373 results on '"G Dobos"'
Search Results
2. Actinic cheilitis: a systematic review of treatment options
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G. Dobos, Martine Bagot, Jean-David Bouaziz, Céleste Lebbé, A. de Masson, F. Herms, Larisa J. Geskin, K. Farmer, Claas Ulrich, Nicole Basset-Seguin, and Megan H. Trager
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medicine.medical_specialty ,Skin Neoplasms ,Chemical peel ,MEDLINE ,Dermatology ,Cochrane Library ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Carcinoma ,Humans ,Medicine ,Prospective Studies ,Adverse effect ,Prospective cohort study ,business.industry ,Actinic cheilitis ,Treatment options ,medicine.disease ,Infectious Diseases ,Cheilitis ,030220 oncology & carcinogenesis ,Carcinoma, Squamous Cell ,Neoplasm Recurrence, Local ,business - Abstract
Actinic cheilitis is a premalignant condition that can progress to squamous cell carcinoma with a higher propensity for metastasis than cutaneous squamous cell carcinoma. Optimal treatment for actinic cheilitis has not been established, and evidence-based estimates of clinical cure in the dermatology literature are limited. Here, we review and synthesize outcome data published for patients with actinic cheilitis after treatment with various modalities. A systematic review was conducted in MEDLINE, Embase and the Cochrane library for English, French and German-language studies and references of included articles from inception to 20 January 2020. Studies were included if they reported on at least six patients with biopsy-proven actinic cheilitis. After quality appraisal, results of studies with the strongest methodology criteria were synthesized. 18 studies of 411 patients (published 1985 to 2016) were included. The majority of the studies were case series. Carbon dioxide laser ablation and vermilionectomy were associated with the most favourable outcomes with fewest recurrences. Chemical peel and photodynamic therapy were associated with higher recurrence. Adverse effects generally resolved in the weeks following treatment and cosmetic outcomes were favourable overall. In conclusion, there is a lack of high-quality comparative studies evaluating different treatment options for actinic cheilitis. The included publications used various outcome measures; however, the majority reported on the recently defined core outcome sets. These results suggest that both carbon dioxide laser ablation and vermilionectomy are effective treatments for actinic cheilitis. Prospective head-to-head studies are needed to compare these treatment modalities and to assess patient preferences.
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- 2020
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3. Revue systématique de la littérature des cas de mycosis fongoïde chalazodermique et de ses options thérapeutiques
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G. Battesti, C. Ram-Wolff, G. Dobos, E. Guenova, J.D. Bouaziz, S. Mourah, J.M. Cayuela, H. Moins-Teisserenc, M. Battistella, M.D. Vignon-Pennamen, J. Rivet, M. Bagot, and A. De Masson
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Ocean Engineering ,Safety, Risk, Reliability and Quality - Published
- 2022
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4. CCR8 : nouvelle cible thérapeutique dans les lymphomes T cutanés
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A. de Masson, J. Giustiniani, G. Dobos, H. Moins-Teisserenc, M. Battistella, N. Ortonne, C. Ram-Wolff, J.D. Bouaziz, S. Mourah, A. Marie-Cardine, M. Bagot, T. Kupper, R. Clark, and A. Bensussan
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Ocean Engineering ,Safety, Risk, Reliability and Quality - Published
- 2022
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5. Yield and quality of grain amaranth (Amaranthus sp.) in Eastern Austria
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D.M. Gimplinger, G. Dobos, R. Schönlechner, and H.-P. Kaul
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amaranthus ,genotype ,plant density ,grain yield ,water content ,thousand seed weight ,chemical composition ,microbial infestation ,germination ,Plant culture ,SB1-1110 - Abstract
The introduction of a new crop requires adapted genotypes as well as optimum crop management practices. This study was conducted to determine the optimum crop density of adapted grain amaranth genotypes in the Pannonian region of Eastern Austria. The genotypes Neuer Typ (A. hypochondriacus), Mittlerer Typ (A. hypochondriacus) and Amar (A. cruentus) were established at plant densities of 8, 17 and 35 plants/m2 in 2002 and 2003. Average hand-harvested yields ranged from 2200 to 3000 kg/ha without significant genotypic differences. Genotypes differed in thousand seed weight (0.55-1.04 g), time from sowing to harvest (97-130 days), grain water content at harvest (24-38%), microbial infestation of air-dried grain (0.2-118.6 cfu × 106/g), germination (29-79%) and grain composition. Grain contents fell within the following ranges: crude protein 15.2-18.6%, crude fat 5.4-8.6%, crude fibre 3.5-4.2%, ash 2.7-3.2%, and carbohydrates 66.7-72.7%. High grain water contents involved stronger microbial infestation and reduced germination. Crop density affected neither grain yield nor grain quality.
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- 2007
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6. Quantifying response to various treatments using the revisited blood staging of mycosis fungoides and Sézary syndrome with the KIR3DL2 marker
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Marie Roelens, Maryam Miladi, G. Dobos, Hélène Moins-Teisserenc, Martine Bagot, Maxime Battistella, Adèle de Masson, Armand Bensussan, Caroline Ram-Wolff, Samia Mourah, and Laurence Michel
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Cancer Research ,Mycosis fungoides ,Pathology ,medicine.medical_specialty ,Oncology ,KIR3DL2 ,medicine.diagnostic_test ,business.industry ,medicine ,Biomarker (medicine) ,medicine.disease ,business ,Flow cytometry - Published
- 2021
7. 464 CCR8 is a new therapeutic target in cutaneous T-cell lymphomas
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A. de Masson, G. Dobos, H. Moins-Teisserenc, M. Battistella, N. Ortonne, M. Bagot, T. Kupper, R.A. Clark, A. Bensussan, and J. Giustiniani
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Cell Biology ,Dermatology ,Molecular Biology ,Biochemistry - Published
- 2022
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8. Immunophenotypic identification and characterization of CTCL tumor cells in blood using standardized flow cytometry: a European multicenter study
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S Najidh, AJ Van der Sluijs Gelling, A Cozzio, G Dobos, M Bagot, M Beylot-Barry, E Guenova, J Nicolay, M Lima, PL Ortiz-Romero, E Papadavid, R Pujol, P Quaglino, R Stadler, U Wehkamp, S Whittaker, JJM Van Dongen, J Flores Montero, J Almeida, and MH Vermeer
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Cancer Research ,Oncology - Published
- 2022
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9. Primary cutaneous gamma-delta lymphoma responding only to mogamulizumab and total skin electron beam therapy
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M Kinberger, F Ghoreschi, R Moritz, M Schlaak, K Meier, and G Dobos
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Cancer Research ,Oncology - Published
- 2022
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10. Early detection of relapse in Sézary syndrome: the added value of KIR3DL2, T-plastin, Twist and Tox for clinical routine
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G Dobos, C Ram-Wolff, H Moins, A de Masson, A Bensussan, M Bagot, and L Michel
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Cancer Research ,Oncology - Published
- 2022
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11. Time to next treatment in early-stage mycosis fungoides: a retrospective study from the Charité cutaneous lymphoma registry
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S Schulz, R Cankaya, F Walter, R Moritz, M Schlaak, T Eigentler, and G Dobos
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Cancer Research ,Oncology - Published
- 2022
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12. Kaposi sarcoma in a patient with Sézary syndrome
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CM Rose Kathrin, M Zidane, RU Reidel, and G Dobos
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Cancer Research ,Oncology - Published
- 2022
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13. Distinction between CTCL and inflammatory dermatoses using mRNA expression of cancer-associated fibroblast markers from skin biopsies
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G Dobos, M Battistella, C Ram-Wolff, K Seerror, A de Masson, D Boccara, M Mimoun, M Bagot, and A Bensussan
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Cancer Research ,Oncology - Published
- 2022
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14. Durable complete remission in Sézary syndrome using extracorporal photopheresis: the role of maintenance treatment on a case series
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M Zidane, R Moritz, U Reidel, M Schlaak, and G Dobos
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Cancer Research ,Oncology - Published
- 2022
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15. Skin directed therapy superior to systemic treatment in primary cutaneous B-cell lymphoma? A study from the Charité cutaneous lymphoma registry on time to next treatment
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R Cankaya, S Schulz, R Moritz, F Walter, M Schlaak, T Eigentler, and G Dobos
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Cancer Research ,Oncology - Published
- 2022
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16. 847P Precision oncology for resistant acral, mucosal and cutaneous melanomas: A prospective broad high throughput genomics feasibility study
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S. Leyvraz, M. Schütte, T. Kessler, M. Lamping, S. Burock, S. Ochsenreither, V. Amstislavskiy, T. Risch, I. Jelas, C. Ulrich, G. Dobos, F. Klauschen, R. Schäfer, B. Lange, K. Klinghammer, M-L. Yaspo, and U. Keilholz
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Oncology ,Hematology - Published
- 2022
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17. Éruptions granulomateuses associées au mogamulizumab mimant un mycosis fongoïde. Six observations
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Martine Bagot, Jana Al Hage, Maxime Battistella, Marie-Dominique Vignon-Pennamen, Hélène Moins-Teisserenc, Adèle De Masson, Samia Mourah, Caroline Ram-Wolff, Marie Boisson, Jacqueline Rivet, G. Dobos, Aurélie Sadoux, and Jingying Wang
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Ocean Engineering ,Safety, Risk, Reliability and Quality - Published
- 2021
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18. Transcriptomic changes during stage progression of mycosis fungoides: from translational analyses to their potential clinical implications
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Chalid Assaf and G. Dobos
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Proteomics ,Oncology ,medicine.medical_specialty ,Mycosis fungoides ,Skin Neoplasms ,Dermatology ,Biology ,medicine.disease ,Transcriptome ,Mycosis Fungoides ,Internal medicine ,medicine ,Humans ,Stage (cooking) - Published
- 2021
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19. Exploring the role of the skin microenvironment in cutaneous T-cell lymphoma using single cell RNA-sequencing
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G. Dobos, Caroline Ram-Wolff, Martine Bagot, Adèle de Masson, Jean-David Bouaziz, A. Calugareanu, Maxime Battistella, Armand Bensussan, and Laurence Michel
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Cancer Research ,Mycosis fungoides ,medicine.anatomical_structure ,Oncology ,Cell ,Cutaneous T-cell lymphoma ,Cancer research ,medicine ,RNA ,Biology ,medicine.disease - Published
- 2021
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20. Granulomatous slack skin: clinical retrospective study of 8 cases of the Cutaneous Lymphoma French Study Group
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Jean-Michel Cayuela, Philippe Courville, Gilles Battesti, Hélène Moins-Tesserenc, Jacqueline Rivet, M.-P. Algros, Martine Bagot, Adèle de Masson, Caroline Ram-Wolff, Samia Mourah, Maxime Battistella, Pascal Joly, Emmanuella Guenova, G. Dobos, François Aubin, and Marie-Dominique Vignon-Pennamen
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Cancer Research ,Mycosis fungoides ,medicine.medical_specialty ,Oncology ,business.industry ,medicine ,Granulomatous slack skin ,Retrospective cohort study ,medicine.disease ,business ,Dermatology ,Cutaneous lymphoma - Published
- 2021
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21. Macrophage-derived CXCL9 and CXCL11 recruit CD8 T cells in skin and provide long-term disease control in mogamulizumab-treated CTCL patients
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Hélène Moins-Teisserenc, Jean-David Bouaziz, Marie Roelens, G. Dobos, Samia Mourah, Aurélie Sadoux, Delphine Darbord, Marie Boisson, Martine Bagot, Hélène Le Buanec, Anne Marie-Cardine, Maxime Battistella, Charles Cassius, Adèle de Masson, Caroline Ram-Wolff, Baptiste Louveau, Pierre de la Grange, and Fanélie Jouenne
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Cancer Research ,Oncology ,business.industry ,Immunology ,Mogamulizumab ,medicine ,CXCL9 ,Cytotoxic T cell ,Macrophage ,CXCL11 ,business ,Disease control ,medicine.drug - Published
- 2021
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22. Case 41. Cutaneous Epstein–Barr Virus post-transplant lymphoproliferative disorder
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Marisa Battistella, Caroline Ram-Wolff, Pauline Brice, David Michonneau, Martine Bagot, G. Dobos, R. Peffault de Latour, and A. de Masson
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business.industry ,Immunology ,Medicine ,business ,medicine.disease_cause ,medicine.disease ,Epstein–Barr virus ,Post-transplant lymphoproliferative disorder - Published
- 2021
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23. Vieillissement cutané
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G. Dobos, E. Zuelgaray, Armand Bensussan, Laurence Michel, Kevin Serror, Françoise Boismal, Hopital Saint-Louis [AP-HP] (AP-HP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Immunologie humaine, physiopathologie & immunothérapie (HIPI (UMR_S_976 / U976)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP), Institut de Recherche Saint-Louis - Hématologie Immunologie Oncologie (Département de recherche de l’UFR de médecine, ex- Institut Universitaire Hématologie-IUH) (IRSL), and Université de Paris (UP)
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0303 health sciences ,business.industry ,Vaccine response ,[SDV]Life Sciences [q-bio] ,General Medicine ,Immunosenescence ,General Biochemistry, Genetics and Molecular Biology ,Pathophysiology ,3. Good health ,Skin Aging ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Innovative Therapies ,Immune system ,Medicine ,business ,Skin pathology ,Neuroscience ,030304 developmental biology - Abstract
Un des enjeux majeurs de ce XXIesiècle est la lutte contre le vieillissement, défini comme un ensemble de mécanismes physiologiques altérant les capacités physiques et intellectuelles de l’organisme. Le vieillissement de la peau n’est qu’un trait visible de ce processus. Il est associé à des défauts de cicatrisation majeurs liés à l’altération des propriétés biomécaniques des cellules cutanées, essentiellement des fibroblastes dermiques. Le système immunitaire, autre composante clé du maintien de l’homéostasie cutanée et du bon déroulement de la cicatrisation des plaies, subit aussi les effets du temps : l’immunosénescence cutanée consécutive limiterait la réponse anti-infectieuse et vaccinale, tout en favorisant un environnement pro-tumoral. Les principales atteintes cutanées dues au vieillissement, que celui-ci soit intrinsèque ou extrinsèque, seront détaillées avant d’énumérer les stratégies anti-âges efficaces pour lutter contre les stigmates dermiques et épidermiques liées à l’âge.
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- 2020
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24. Epidemiology of Cutaneous T-Cell Lymphomas: A Systematic Review and Meta-Analysis of 16,953 Patients
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Jean-David Bouaziz, G. Dobos, Martine Bagot, Caroline Ram-Wolff, Anne Pohrt, Céleste Lebbé, Maxime Battistella, and Adèle de Masson
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Cancer Research ,medicine.medical_specialty ,skin ,T cell ,MEDLINE ,Cochrane Library ,lymphomas ,lcsh:RC254-282 ,Article ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,systematic review ,hemic and lymphatic diseases ,cutaneous T-cell lymphomas ,Epidemiology ,medicine ,Mycosis fungoides ,business.industry ,mycosis fungoides ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,medicine.disease ,Dermatology ,Lymphoma ,Systematic review ,medicine.anatomical_structure ,Oncology ,030220 oncology & carcinogenesis ,Meta-analysis ,business - Abstract
Cutaneous T-cell lymphomas (CTCL) are a heterogenous group of rare diseases. Many studies have reported on local epidemiology or geographic clustering, however we lack information from a global perspective. A systematic review and meta-analysis was conducted in Medline and the Cochrane Library based on a previously registered protocol and according to the preferred reporting of items for systematic reviews and meta-analyses (PRISMA). We selected publications that enrolled at least 100 patients with primary cutaneous lymphomas according to the current classifications. The relative frequencies (proportions) of subtypes were compared between studies and geographic regions in a meta-analysis. In total, 26 studies met our inclusion criteria, reporting on altogether 16,953 patients. Within primary cutaneous lymphomas, CTCL appeared to be 15% more frequent in Asian populations. Mycosis fungoides (MF) accounted for 62% of CTCL, with an important heterogeneity in frequencies between studies and continents. The proportion of Sé, zary syndrome (SS) was 3%, stable worldwide. Rare CTCL, such as NK/T-cell lymphoma or subcutaneous panniculitis-like lymphoma, were more frequent in Asian studies. This global meta-analysis of CTCL confirmed the predominance of CTCL among primary cutaneous lymphomas (83% on average) in the three analyzed continents, most of which were MF cases. It revealed the same proportions of SS across continents, and the heterogeneity of MF frequencies, suggesting the possible role of environmental factors in the pathophysiology of the latter. Registration number: CRD42020148295 (PROSPERO).
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- 2020
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25. Lupus Erythematosus Tumidus Mimicking Primary Cutaneous Marginal Zone B-cell Lymphoma
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Larisa J. Geskin, Caroline Ram-Wolff, Jean-David Bouaziz, Maxime Battistella, Marie-Dominique Vignon-Pennamen, Adèle de Masson, Martine Bagot, Pauline Brice, Jacqueline Rivet, G. Dobos, and Megan H. Trager
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Pathology ,medicine.medical_specialty ,Systemic lupus erythematosus ,Hardware_MEMORYSTRUCTURES ,Skin Neoplasms ,business.industry ,lymphoma ,Dermatology ,General Medicine ,lupus ,Lymphoma, B-Cell, Marginal Zone ,lcsh:RL1-803 ,medicine.disease ,Lupus Erythematosus Tumidus ,Hodgkin Disease ,Lymphoma ,Lupus Erythematosus, Discoid ,medicine ,lcsh:Dermatology ,Lupus Erythematosus, Cutaneous ,Humans ,business ,clinical challenge ,Primary cutaneous marginal zone B-cell lymphoma - Abstract
is missing (Short communication)
- Published
- 2020
26. Diagnostic performance of high‐throughput sequencing of the T‐cell receptor beta gene for the diagnosis of cutaneous T‐cell lymphoma
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Marisa Battistella, Céleste Lebbé, Jacqueline Rivet, Baptiste Louveau, Samia Mourah, Jean Michel Cayuela, Aurélie Sadoux, C. Zimmermann, G. Dobos, A. de Masson, M.-D. Vignon-Pennamen, Caroline Ram-Wolff, Aurélia Gruber, Martine Bagot, Hélène Moins-Teisserenc, Marie Boisson, and Marie Roelens
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Skin Neoplasms ,business.industry ,T-Cell Receptor Beta Gene ,T cell ,Cutaneous T-cell lymphoma ,High-Throughput Nucleotide Sequencing ,Dermatology ,medicine.disease ,DNA sequencing ,Lymphoma, T-Cell, Cutaneous ,Lymphoma ,T-Cell Receptor Beta ,medicine.anatomical_structure ,Text mining ,Genes, T-Cell Receptor beta ,Cancer research ,Humans ,Medicine ,business ,Gene - Published
- 2021
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27. Recent advances on cutaneous lymphoma epidemiology
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G. Dobos, M. Miladi, L. Michel, C. Ram-Wolff, M. Battistella, M. Bagot, and A. de Masson
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Lymphoma, B-Cell ,Skin Neoplasms ,Humans ,General Medicine ,Prognosis ,Biomarkers ,Lymphoma, T-Cell, Cutaneous - Abstract
Primary cutaneous lymphomas are a group of T- (CTCL) and B-cell (CBCL) malignancies. These diseases have different clinical presentations and prognosis. Our knowledge on their epidemiology is limited. Aim of this review was to summarize recent findings on the incidence of CTCL and CBCL, how they change over time, and to describe possible causes and consequences. We found that although there are important differences in the epidemiology of cutaneous lymphomas in different countries, the relative frequency of certain, especially rare lymphomas remains stable. Several studies described growing incidences of both CTCL and CBCL. The emergence of new diagnostic criteria, a more precise definition of the entities and new biomarkers enable a better classification of cases.
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- 2022
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28. Performances du séquençage haut débit du TCR-bêta pour le diagnostic de lymphome T cutané
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Jean-Michel Cayuela, Céleste Lebbé, Marie-Dominique Vignon-Pennamen, Hélène Moins-Teisserenc, Maxime Battistella, Aurélia Gruber, Marie Boisson, Jacqueline Rivet, Marie Roelens, Samia Mourah, Aurélie Sadoux, Caroline Ram Wolff, Baptiste Louveau, G. Dobos, Martine Bagot, Adèle de Masson, and Clement Zimmermann
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Ocean Engineering ,Safety, Risk, Reliability and Quality - Abstract
Introduction Le diagnostic precoce de lymphome T cutane n’est pas toujours aise et repose sur un faisceau d’arguments cliniques, biologiques, histologiques et moleculaires. Le sequencage haut debit du TCR-beta permet par la reconnaissance de sequences CDR3 specifiques l’identification et la quantification de chaque clone T present dans un echantillon donne. Il existe encore peu d’etudes a ce sujet avec des resultats discordants et aucun critere diagnostic valide. Notre etude avait comme but de determiner pour cette technique des seuils optimaux pour les valeurs suivantes : frequence du clone T majoritaire dans la peau rapportee a l’echantillon total (TCF) et ratio entre la frequence du premier et du deuxieme clone T (RPF), avec comme objectif de developper de nouveaux algorithmes pour le diagnostic de lymphome T cutane. Materiel et methodes Nous avons analyse retrospectivement les donnees obtenues par le sequencage haut debit du TCR-beta dans des echantillons de biopsies cutanees realisees chez 144 patients entre 2013 et 2020. Le diagnostic de lymphome T cutane etait base sur des criteres internationaux valides. Nous avons inclus 101 echantillons de patients ayant un diagnostic de lymphome T confirme dont 47 MF stade I-IIA, 1 stade IIB, 4 stade III, 35 syndromes de Sezary, 8 lymphomes T agressifs (PTCL NOS ou CD8+) et 6 lymphoproliferations CD30+ (3 papuloses lymphomatoides et 3 lymphomes anaplasiques a grandes cellules). En complement 43 echantillons provenant de patients avec des pathologies inflammatoires etaient inclus. Les performances de la technique ont ete etudiees a l’aide de courbes ROC. Resultats Les meilleures performances diagnostiques etaient obtenues pour le TCF avec une AUC de 0,957 versus 0,929 pour le RPF. Les valeurs de TCF et RPF pour chaque categorie ont ete modelisees. Avec des seuils de TCF de 5 % et 25 %,la specificite pour le diagnostic etait de 95 % et 100 %, et la sensibilite de 89 % et 50 %. Il existait une correlation significative entre le TCF et l’importance de l’atteinte sanguine chez les patients SS (cellules TCD4 + CD26−, r = 0,59, p = 0,0008 ; T CD4 + CD7−, r = 0,45, p = 0,01 ; T CD4 + CD158k+, r = 0,4, p = 0,03) Discussion Le TCF obtenu par HTS-TRB est un critere robuste pour le diagnostic de lymphome T cutane et particulierement pour celui de MF, avec une sp de 95 % et une se de 89 % pour un seuil de 5 %. Une telle specificite permettrait un diagnostic precoce de lymphome T cutane dans des cas difficiles. Ces resultats sont meilleurs que ceux obtenus a l’aide de la PCR classique sur gel du TCR gamma qui sont entaches de nombreux faux negatifs et faux positifs. Des etudes multicentriques prospectives seraient necessaires pour la definition de criteres valides internationaux pour l’usage de cette technique dans le diagnostic de lymphome T cutane.
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- 2021
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29. Treatment efficacy for Sézary syndrome: an international, multi-centre, comparative study of current systemic therapies
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Belinda A. Campbell, Zahra Haider, Julia Scarisbrick, Caroline Ram-Wolff, H. Miles Prince, Martine Bagot, Christopher McCormack, Maryam Miladi, and G. Dobos
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Cancer Research ,Mycosis fungoides ,Chemotherapy ,medicine.medical_specialty ,Combination therapy ,business.industry ,medicine.medical_treatment ,medicine.disease ,Systemic therapy ,Clinical trial ,Oncology ,Internal medicine ,Clinical endpoint ,Medicine ,Methotrexate ,Stage (cooking) ,business ,medicine.drug - Abstract
Background: Despite increasing availability of therapeutic agents, Sezary syndrome (SS) remains associated with a generally poor prognosis. Typically, patients endure multi-line treatment, frequently with disappointingly short durations of clinical benefit. Time to next treatment (TTNT) measures the interval from the date of commencement of one therapy to the date of initiation of the next line of therapy, and provides a simple and reliable surrogate for duration of clinical benefit outside of clinical trials [ 1 ]. In this multi-centre collaborative study, we review the clinical outcomes of patients with SS/ mycosis fungoides (MF) with B1-2 blood involvement, and compare the treatment efficacy of the currently available systemic therapies using TTNT. Methods: In this retrospective analysis, eligible patients were identified from University Hospital Birmingham, Birmingham, Peter MacCallum Cancer Centre, Melbourne, and Hopital Saint Louis, Paris. Strict eligibility required biopsy-proven MF/SS, with B1-2 blood involvement, newly diagnosed during 1/1/2012 to 31/12/2020. Studied treatment groups include monotherapy and combination therapies of interferon, methotrexate, ECP, HDAC inhibitors, retinoids, monoclonal antibodies, biologicals, chemotherapy, allogeneic stem cell transplant, and best supportive care. The primary endpoint was TTNT, with the aim to compare the efficacy of these systemic therapies. Results: 178 patients were eligible. 77 (43%) were female, median age was 66 (17–94) years. At diagnosis, 35 (20%) patients had Stage IIIB, 131 (74%) Stage IVA and 12 (7%) Stage IVB MF/SS. Large cell transformation was present in 35 (20%) patients at time of diagnosis. A total of 802 treatment lines were delivered, of which 711 were systemic therapies and were included for analysis. Of the 178 patients, 168 received systemic therapy first-line: the most commonly delivered first-line systemic treatments were ECP-containing regimens in 42 (25%) patients (ECP-monotherapy, 17, ECP-based combination therapy, 25), retinoid monotherapy in 34 (19%), interferon monotherapy in 25 (14%) and methotrexate monotherapy in 25 (14%) patients. TTNT and overall survival data will be presented. Conclusions: As a surrogate for duration of clinical benefit, TTNT is a useful endpoint to retrospectively compare the treatment efficacy of currently available systemic therapies for SS/MF with B1-2 blood involvement. Long-term disease control with durable clinical benefit remains the ultimate goal for patients with SS/MF with blood involvement.
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- 2021
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30. Secretomic and proteomic analysis of cutaneous T cell lymphoma-associated fibroblasts
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Jean-Marie Camadro, Sophie Ly Ka So, Françoise Boismal, G. Dobos, M. Mimoun, Kevin Serror, Martine Bagot, Armand Bensussan, and Laurence Michel
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Cancer Research ,Tumor microenvironment ,Chemistry ,Mesenchymal stem cell ,Cutaneous T-cell lymphoma ,medicine.disease ,medicine.disease_cause ,Metastasis ,Lymphoma ,medicine.anatomical_structure ,Oncology ,hemic and lymphatic diseases ,Proteome ,medicine ,Cancer research ,Carcinogenesis ,Fibroblast - Abstract
Introduction: Cancer-associated fibroblasts (CAFs), a component of tumor microenvironment, play a key role in oncogenesis and promote growth, invasion, metastasis and chemo-resistance of tumor cells. Our previous RNAseq results brought evidence of the contribution of dermal fibroblasts obtained from cutaneous T-cell lymphoma (CTCL) lesions to support tumor growth. Here, we further go on by analyzing the alteration of protein production by dermal fibroblasts obtained from CTCL lesions versus control fibroblasts. Materials and methods: Secretome and proteome was performed on fibroblast primary cultures skin biopsies of 6 cutaneous T-cell lymphoma (CTCL[GD1]) versus fibroblasts from healthy mammary skin controls (age-paired). The fibroblasts of the two groups were studied at the 3rd passage, after stimulation or not with 5 ng/ml TGF-β for 24 h. The supernatants and lysates collected underwent enzymatic digestion with trypsin before peptide analysis by HLPC/Mass spectrometry Results: The comparison of the secretomes from the CTCL groups (± TGF-s) and the control donors showed a global significant differential expression (fold >2, p-value 2, p-value Conclusion: The present data demonstrate the potent proteomic alteration of CTCL-associated dermal fibroblasts, confirming the involvement of mesenchymal cells on the behavior of CTCL.
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- 2021
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31. Granulomatous rash associated with mogamulizumab mimicking mycosis fungoides: a case series
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Jana Al Hage, Jacqueline Rivet, Adèle de Masson, Martine Bagot, Maxime Battistella, Marie-Dominique Vignon-Pennamen, Marie Boisson, Aurélie Sadoux, Samia Mourah, Caroline Ram-Wolff, Hélène Moins-Teisserenc, G. Dobos, and Jingying Wang
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Cancer Research ,Mycosis fungoides ,medicine.medical_specialty ,Oncology ,business.industry ,Mogamulizumab ,medicine ,medicine.symptom ,medicine.disease ,business ,Rash ,Dermatology ,medicine.drug - Published
- 2021
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32. 267 Characterization of Cancer-Associated Fibroblasts from Mycosis Fungoides and Sézary syndrome
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Habib Zouali, Caroline Ram-Wolff, M. Mimoun, A. de Masson, Martine Bagot, K. Serror, G. Dobos, Laurence Michel, Jean-François Deleuze, and S. Ly Ka So
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Mycosis fungoides ,business.industry ,Cancer research ,medicine ,Cancer-Associated Fibroblasts ,Cell Biology ,Dermatology ,medicine.disease ,business ,Molecular Biology ,Biochemistry - Published
- 2021
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33. Diagnostic performance of high throughput sequencing of the T-cell receptor beta gene for the diagnosis of cutaneous T-cell lymphoma
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Hélène Moins-Teisserenc, Aurélia Gruber, Céleste Lebbé, Adèle de Masson, Dominique Vignon, Jean-Michel Cayuela, Aurélie Sadoux, Martine Bagot, Samia Mourah, Maxime Battistella, Clement Zimmermann, Caroline Ram-Wolff, Jacqueline Rivet, Marie Boisson, G. Dobos, Baptiste Louveau, and Marie Roelens
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Cancer Research ,Oncology ,T-Cell Receptor Beta Gene ,Cutaneous T-cell lymphoma ,medicine ,Cancer research ,Biology ,medicine.disease ,DNA sequencing - Published
- 2021
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34. The effectiveness of standardized skin care regimens on skin dryness in nursing home residents: A randomized controlled parallel-group pragmatic trial
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Jan Kottner, Ulrike Blume-Peytavi, Natalie Garcia Bartels, Andrea Lichterfeld-Kottner, Andrea Stroux, Anja Klasen, Heike Neels-Herzmann, Elisabeth Hahnel, Carina Trojahn, G. Dobos, and Irina Jahnke
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Male ,medicine.medical_specialty ,Cutis ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Dry skin ,medicine ,Humans ,030212 general & internal medicine ,General Nursing ,Aged ,Aged, 80 and over ,Skin care ,Inpatients ,integumentary system ,business.industry ,Ichthyosis ,Trunk ,Pragmatic trial ,Nursing Homes ,Clinical trial ,Physical therapy ,Dryness ,Female ,medicine.symptom ,Nursing homes ,business - Abstract
Background Aged residents of institutional long-term care facilities are at high risk for developing skin and tissue diseases. Besides various common skin problems, dry skin (xerosis cutis) is one of the most frequent skin conditions in this setting. Objectives To investigate the effectiveness of two structured skin care regimens in comparison to routine skin care on xerosis cutis in nursing home residents. Design A multi-center, pragmatic, randomized, controlled, investigator blinded study with three parallel groups. Settings The study was conducted in a random sample of ten out of 291 institutional long-term care facilities of the federal state of Berlin, Germany. Participants Long-term care residents being 65+ years affected by dry skin were included. Methods The residents were allocated into one of three study groups. Two interventional groups used standardized skin care regimens, consisting of a body wash and twice daily applications of leave-on products for eight weeks. The third control group performed skin care as usual. All participating residents were examined at baseline and after 4 and 8 weeks. Xerosis cutis was measured with the Overall Dry Skin score. Instrumental skin barrier measurements were performed at baseline and after 8 weeks. Diaries were used to document washing and skin care frequencies. Results In total, 133 residents were included and allocated to one of the three groups. Mean age was 83.8 (SD 8.3) years, 65.4% were female and most residents had care levels I (42.9%) or II (42.9%) according to the German Social Code Book XI. Mean Barthel score was 46.8 (SD 24.2) and mean Braden score was 17.6 (SD 3.7). Leg skin areas were drier compared to arms and trunk areas. At the end of the study the Overall Dry Skin scores in the intervention groups were lower compared to the control group. There were statistically significant improvements of skin dryness in both intervention groups compared to the control group over time. Conclusions The results of this pragmatic trial indicate that structured skin care regimens are effective in reducing skin dryness in aged nursing home residents within eight weeks. Trial registration The study is registered at https://clinicaltrials.gov/ct2/show/NCT02216526.
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- 2017
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35. Changements dans l’épidémiologie des lymphomes cutanés primitifs en France : une analyse de 8593 patients du registre du Groupe Français d’Etude des Lymphomes Cutanés (GFELC)
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Michel D'Incan, Anne Durlach, E. Maubec, Anne Pham-Ledard, Liliane Laroche, Saskia Oro, A. de Masson, Stéphane Barete, Caroline Ram-Wolff, Martine Bagot, Florent Amatore, T. Petrella, Nathalie Franck, Florent Grange, Groupe français d’étude des lymphomes cutanés, Marie Beylot-Barry, Jacques Rouanet, Nicolas Ortonne, Isabelle Templier, Laurent Mortier, Isabelle Moulonguet, Charlée Nardin, B. Vergier, Laurence Lamant, Serge Boulinguez, Romain Dubois, Jacqueline Rivet, Agnès Carlotti, N. Josselin, Laurence Michel, F. Franck, M.-D. Vignon-Pennamen, O. Dereur, Gaëlle Quéreux, Philippe Courville, Marisa Battistella, Pascal Joly, S. Taix, Sophie Dalac, O. Augereau, and G. Dobos
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Dermatology - Abstract
Introduction Les lymphomes cutanes primitifs sont un groupe heterogene de lymphomes T cutanes (LTC) et de lymphomes B cutanes (LBC). Nous avons peu dinformations sur les caracteristiques des patients atteints de ces maladies et leurs stades initiaux. Malgre plusieurs publications nationales europeennes il existe peu de donnees sur ĺevolution de leur epidemiologie au cours du temps. Le but de cette etude etait de comparer ĺepidemiologie, les caracteristiques et la demographie des patients atteints dun lymphome cutane primitif au cours des quinze dernieres annees et dinvestiguer d’eventuels changements. Materiel et methodes Nous avons inclus les patients ayant eu un diagnostic de lymphome cutane primitif selon les criteres de ĺEORTC-OMS entre 2005 et 2019. Les patients ont ete tries en 3 groupes definis par leur periode d’inclusion (2005–2009, 2010–2014 et 2015–2019) pour les comparer. Resultats Le nombre total de patients inclus a augmente annuellement. Ĺincidence calculee des lymphomes cutanes primitifs etait de 1,06/100 000 habitants en France, ce qui est plus eleve que ce qui a ete decrit dans la litterature. La majorite des lymphomes cutanes etaient plus frequents chez les hommes a un âge moyen de 60 ans. La frequence relative des LTC etait stable, la proportion du mycosis fongoide classique avait diminue et la proportion des autres variants etait croissante (par exemple le mycosis fongoide folliculotrope). Des tendances similaires ont ete observees pour les lymphomes B cutanes, la frequence relative des lymphomes B de la zone marginale etait croissante. Discussion Les changements de frequence des lymphomes cutanes peuvent etre expliques par ĺemergence de nouveaux criteres diagnostiques et des definitions plus precises de ces maladies dans la nouvelle classification. Cest la premiere etude a demontrer des changements de ĺepidemiologie des lymphomes cutanes primitifs au cours du temps.
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- 2020
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36. Epidemiological changes in cutaneous lymphomas: an analysis of 8593 patients from the French Cutaneous Lymphoma Registry
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Nicolas Franck, E. Maubec, Gaëlle Quéreux, Caroline Ram-Wolff, Philippe Courville, Laurence Lamant, Olivier Dereure, G. Dobos, Isabelle Templier, Florent Grange, Saskia Ingen-Housz-Oro, Jacques Rouanet, Martine Bagot, N. Josselin, O. Augereau, Stéphane Barete, Serge Boulinguez, Isabelle Moulonguet, Marisa Battistella, Nicolas Ortonne, Anne Durlach, A. Carlotti, Pascal Joly, S. Taix, Sophie Dalac, Michel D'Incan, F. Franck, Laurent Mortier, A. de Masson, Marie Beylot-Barry, Charlée Nardin, Jacqueline Rivet, M.-D. Vignon-Pennamen, Laurence Michel, Liliane Laroche, Anne Pham-Ledard, Romain Dubois, T. Petrella, Béatrice Vergier, Florent Amatore, Service de Dermatologie [AP-HP Hôpital Saint-Louis], Hopital Saint-Louis [AP-HP] (AP-HP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Immunologie humaine, physiopathologie & immunothérapie (HIPI (UMR_S_976 / U976)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP), Service de dermatologie [Bordeaux], Université Bordeaux Segalen - Bordeaux 2-CHU Bordeaux [Bordeaux]-Hôpital Haut-Lévêque [CHU Bordeaux], CHU Bordeaux [Bordeaux], Département de pathologie [Mondor], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Imagerie Moléculaire et Stratégies Théranostiques (IMoST), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020]), CHU Gabriel Montpied [Clermont-Ferrand], CHU Clermont-Ferrand, Service de Dermatologie [CHU Cochin], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Cochin [AP-HP], Hôpital Cochin [AP-HP], Centre hospitalier de Cahors, Institut Universitaire du Cancer de Toulouse - Oncopole (IUCT Oncopole - UMR 1037), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-CHU Toulouse [Toulouse]-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de Pathologie [CHU de Dijon], Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Service de Dermatologie (CHU de Dijon), Service de Dermatologie [Rouen], Hôpital Charles Nicolle [Rouen]-CHU Rouen, Normandie Université (NU)-Normandie Université (NU), Physiopathologie, Autoimmunité, maladies Neuromusculaires et THErapies Régénératrices (PANTHER), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Rouen Normandie (UNIROUEN), Département de Pathologie [CHU Rouen], CHU Rouen, Normandie Université (NU)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Pathogénèse et contrôle des infections chroniques (PCCI), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre Hospitalier Universitaire de Montpellier (CHU Montpellier ), Service de dermatologie, vénéreologie et cancérologie cutanée [Hôpital de la Timone - APHM], Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE), Hôpital de la Timone [CHU - APHM] (TIMONE), Hôpital Robert Debré, Hôpital Robert Debré-Centre Hospitalier Universitaire de Reims (CHU Reims), Pathologies Pulmonaires et Plasticité Cellulaire - UMR-S 1250 (P3CELL), Université de Reims Champagne-Ardenne (URCA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de dermatologie [Nantes], Université de Nantes (UN)-Centre hospitalier universitaire de Nantes (CHU Nantes), Centre hospitalier universitaire de Nantes (CHU Nantes), Hôpital Claude Huriez [Lille], CHU Lille, Thérapies Laser Assistées par l'Image pour l'Oncologie - U 1189 (ONCO-THAI), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Service de pathologie [CHU Lille], Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Service de dermatologie [Avicenne], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Avicenne [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Sorbonne Paris Nord, CHU Grenoble, CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), Interactions hôte-greffon-tumeur, ingénierie cellulaire et génique - UFC (UMR INSERM 1098) (RIGHT), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-Etablissement français du sang [Bourgogne-Franche-Comté] (EFS [Bourgogne-Franche-Comté]), Service de pathologie [Bordeaux], Université Bordeaux Segalen - Bordeaux 2-CHU Bordeaux [Bordeaux]-Groupe hospitalier Pellegrin, Bordeaux Research In Translational Oncology [Bordeaux] (BaRITOn), Université de Bordeaux (UB)-CHU Bordeaux [Bordeaux]-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Centre Hospitalier Cahors, Université de Toulouse (UT)-Université de Toulouse (UT)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Charles Nicolle [Rouen], Normandie Université (NU)-Normandie Université (NU)-CHU Rouen, Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Etablissement français du sang [Bourgogne-Franche-Comté] (EFS BFC)-Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC), and Institut National de la Santé et de la Recherche Médicale (INSERM)-Etablissement français du sang [Bourgogne-Franche-Comté] (EFS [Bourgogne-Franche-Comté])-Université de Franche-Comté (UFC)
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medicine.medical_specialty ,Mycosis fungoides ,Heterogeneous group ,business.industry ,Incidence (epidemiology) ,[SDV]Life Sciences [q-bio] ,CBCL ,Retrospective cohort study ,Dermatology ,medicine.disease ,Cutaneous lymphoma ,3. Good health ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Male patient ,Epidemiology ,medicine ,business ,ComputingMilieux_MISCELLANEOUS - Abstract
Background Primary cutaneous lymphomas (PCLs) are a heterogeneous group of T-cell (CTCL) and B-cell (CBCL) malignancies. Little is known about their epidemiology at initial presentation in Europe and about potential changes over time. Objectives The aim of this retrospective study was to analyse the frequency of PCLs in the French Cutaneous Lymphoma Registry (GFELC) and to describe the demography of patients. Methods Patients with a centrally validated diagnosis of primary PCL, diagnosed between 2005 and 2019, were included. Results The calculated incidence was unprecedently high at 1·06 per 100 000 person-years. The number of included patients increased yearly. Most PCL subtypes were more frequent in male patients, diagnosed at a median age of 60 years. The relative frequency of rare CTCL remained stable, the proportion of classical mycosis fungoides (MF) decreased, and the frequency of its variants (e.g. folliculotropic MF) increased. Similar patterns were observed for CBCL; for example, the proportion of marginal-zone CBCL increased over time. Conclusions Changes in PCL frequencies may be explained by the emergence of new diagnostic criteria and better description of the entities in the most recent PCL classification. Moreover, we propose that an algorithm should be developed to confirm the diagnosis of PCL by central validation of the cases.
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- 2020
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37. Challenges in the diagnosis of primary cutaneous <scp>CD</scp> 30 + anaplastic large‐cell lymphoma
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J.-N. Dauendorffer, Samia Mourah, Céleste Lebbé, Jean Michel Cayuela, Fanélie Jouenne, Martine Bagot, J. Rivet, D. Bouaziz, Marisa Battistella, Caroline Ram-Wolff, F. Herms, M.D. Vignon‐Pennamen, A. de Masson, Pauline Brice, and G. Dobos
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Pathology ,medicine.medical_specialty ,CD30 ,business.industry ,Cutaneous T-cell lymphoma ,Medicine ,Immunohistochemistry ,Dermatology ,CD30+ Anaplastic Large Cell Lymphoma ,business ,Brentuximab vedotin ,medicine.disease ,medicine.drug - Published
- 2019
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38. The effectiveness of using a bath oil to reduce signs of dry skin: A randomized controlled pragmatic study
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G. Dobos, Kathrin Hillmann, Varvara Kanti, Elisabeth Hahnel, Annika Vogt, Andrea Lichterfeld-Kottner, Ulrike Blume-Peytavi, Claudia Richter, and Jan Kottner
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Adult ,Male ,medicine.medical_specialty ,Adolescent ,Bathing ,Cutis ,Young Adult ,030207 dermatology & venereal diseases ,03 medical and health sciences ,Nursing care ,0302 clinical medicine ,Skin Physiological Phenomena ,Skin surface ,Dry skin ,medicine ,Humans ,030212 general & internal medicine ,Child ,General Nursing ,Aged ,Aged, 80 and over ,Skin care ,Transepidermal water loss ,integumentary system ,business.industry ,Infant ,Middle Aged ,Skin Care ,Dermatology ,Clinical trial ,Child, Preschool ,Female ,medicine.symptom ,business ,Oils - Abstract
Background Dry skin (xerosis cutis) is increasingly recognized as a relevant health problem in daily life and in health and nursing care. The use of bath additives such as oils is common to reduce dry skin, but empirical evidence supporting this practice is limited. Objectives The aim of this study was to investigate the effectiveness of using a bath oil additive in improving skin barrier function and ameliorating dry skin in comparison to non-oil containing skin cleansers for bathing or showering. Design Single centre randomized observer blind pragmatic parallel group trial. Settings Outpatient/community care. Participants Volunteers showing clinically mild to moderate dry skin recruited from the city of Berlin. Methods Healthy children and adults were randomly assigned to use either a commercially available bath oil or to continue using their regular non-oil containing skin cleansers every other day over a study period of 28days. Skin barrier parameters and the severity of dry skin were assessed at baseline and at two follow-up visits at the study centre. Transepidermal water loss was the primary outcome. Results All sixty participants randomized completed the trial. Median age was 32.5 (IQR 8.3 to 69) years. At the end of study the mean transepidermal water loss in the intervention group was statistically significant lower compared to the control group (mean difference −1.9 (95% CI −3.1 to −0.8) g/m 2 /h). Stratum corneum hydration was statistically significantly higher in the intervention group at the end of the study. Skin surface pH and roughness were comparable in both groups and remained unchanged, while both groups showed a trend to improvement in dry skin symptoms Conclusions This pragmatic trial provides empirical evidence that the regular use of the investigated bath oil is effective in improving the skin barrier function in children and adults with mild dry skin when used in routine skin care and supports its use as a basic element for the management of a broad spectrum of dry skin conditions. Trial registration ClinicalTrials.gov Identifier NCT02557698.
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- 2017
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39. LB01 SIX WEEKS OF SOFOSBUVIR/LEDIPASVIR TREATMENT OF ACUTE HEPATITIS C VIRUS GENOTYPE 1 MONOINFECTION: FINAL RESULTS OF THE THE GERMAN HEPNET ACUTE HCV IV STUDY
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K. Deterding, C.D. Spinner, E. Schott, T.M. Welzel, G. Gerken, H. Klinker, U. Spengler, J. Wiegand, J. Schulze zur Wiesch, A. Pathil, M. Cornberg, A. Umgelter, C. Zöllner, S. Zeuzem, A. Papkalla, K. Weber, S. Hardtke, H. Leyen, A. Koch, D. Witzendorff, M. Manns, H. Wedemeyer, C.M. Preda, C.P. Popescu, C. Baicus, M. Manuc, R. Voiosu, E. Ceausu, L. Fulger, A. Nisanian, C.S. Pop, A. Oproiu, A. Arezzo, R. Passera, A. Bullano, Y. Mintz, A. KEDAR, L. Boni, E. Cassinotti, R. Rosati, U. Fumagalli, M. Sorrentino, M. Brizzolari, N. Di Lorenzo, A.L. Gaspari, D. Andreone, E. De Stefani, G. Navarra, S. Lazzara, M. Degiuli, K. Shishin, I. Khatkov, I. Kazakov, R. Schrittwieser, T. Carus, A. Corradi, G. Sitzman, A. Lacy, S. Uranues, A. Szold, M.A. Bonino, M. Morino, J. Strömberg, G. Sandblom, R. Coelen, M. Gaspersz, T. Labeur, J. Vugt, S. Dieren, F. Willemssen, C.Y. Nio, J. IJzermans, H.‐J. Klümpen, B. Groot Koerkamp, T. Gulik, R. Sturgess, D. Palmer, J. Trojan, A. Hoffmeister, B. Neu, S. Kasper, A. Dechêne, C. Jürgensen, J. Schirra, R. Jakobs, A. Høgset, L. Finnesand, A.E. Abd Elrazek, S. Saab, T. Salem, M. Abdel‐Aty, B. Hawary, A. Ismail, M. Zayied, M. Alboraie, R. Orenstein, E. Dubberke, C.H. Lee, S. Khanna, G. Hecht, S. Wong, T. Kwong, X. Wang, R.S.Y. Tang, S.C. Ng, J.J.Y. Sung, J. Yu, S. Ott, G.H. Waetzig, A. Rehmann, J. Moltzau‐Anderson, R. Bharti, J.A. Grasis, L. Cassidy, A. Tholey, H. Fickenscher, D. Seegert, P. Rosenstiel, S. Schreiber, T. Mazzawi, G.A. Lied, M. El‐Salhy, O.H. Gilja, J.G. Hatlebakk, T. Hausken, S.T. Witt, O. Bednarska, A. Icenhour, S. Elsenbruch, M. Ström, J.D. Söderholm, M. Engström, E.A. Mayer, Å. Keita, S. Walter, P.K. Kump, P. Wurm, H.P. Gröchenig, H.H. Wenzl, W. Petritsch, B. Halwachs, M. Wagner, V. Stadlbauer‐Köllner, A.J. Eherer, K.M. Hoffmann, A. Deutschmann, G. Reicht, L. Reiter, P. Slawitsch, G. Gorkiewicz, C. Hoegenauer, Y. Zhou, R. Kakuturu, D. Jung, K.K. Jørgensen, I.C. Olsen, G.L. Goll, M. Lorentzen, N. Bolstad, E.A. Haavardsholm, K.E. Lundin, C. Mørk, J. Jahnsen, T.K. Kvien, B.G. Feagan, B.E. Sands, G. Rossiter, X. Li, K. Usiskin, X. Zhan, J.‐F. Colombel, W.J. Sandborn, J. Panés, M. Ferrante, E. Louis, G. D'Haens, D. Franchimont, A. Kaser, O. Dewit, U. Seidler, K.‐J. Kim, M.F. Neurath, P. Scholl, S. Visvanathan, S.J. Padula, I. Herichova, N. Sha, D. Hall, W.O. Böcher, F. Bloemendaal, A. Levin, M. Wildenberg, P. Koelink, S. Verbeek, J. Claassens, B. Mcrae, G. Vidarsson, G.R. Brink, M. Badke, S. Rose‐John, M.E. Spehlmann, L. Peyrin‐Biroulet, J. Gatlin, M. Soloman, D. Unett, H. Al‐Shamma, D. Behan, J. Langhorst, J. Boone, A. Rueffer, G. Dobos, K. Beiderwellen, T. Lauenstein, W.S. Ngu, R. Bevan, Z.P. Tsiamoulos, P. Bassett, Z. Hoare, M. Rutter, N. Totton, T.J. Lee, A.V. Ramadas, J. Silcock, J. Painter, L.J. Neilson, B.P. Saunders, C.J. Rees, A. Schmidt, S. Goelder, H. Messmann, M. Goetz, T. Kratt, A. Meining, M. Birk, J. Delius, M. Albert, J.Y.W. Escher, A. Lau, R. Hoffman, K. Wiest, null Caca, A. Siddiqui, D. Wilson, M. Cangelosi, R. Rameshshanker, P. Wall, K. Cocks, T. Doulton, A. Yusuf, C. Hancock, R. Valori, A. Aravani, J. Rashbass, S. Vernon, E.J.A. Morris, J.H. ‐Choi, D.‐W. Seo, T.J. Song, D.H. Park, S.S. Lee, S.K. Lee, ‐H. Kim, P. Somani, and M. Sharma
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0301 basic medicine ,Ledipasvir ,Sofosbuvir ,business.industry ,Gastroenterology ,Virology ,Virus ,03 medical and health sciences ,chemistry.chemical_compound ,030104 developmental biology ,0302 clinical medicine ,Oncology ,chemistry ,Genotype ,Medicine ,030211 gastroenterology & hepatology ,Acute hepatitis C ,business ,medicine.drug - Published
- 2016
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40. Sensitivity to change of the Dermatology Life Quality Index in adult females with facial acne vulgaris: a validation study
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Annika Vogt, Jan Kottner, Carina Trojahn, Ulrike Blume-Peytavi, Claudia Richter, G. Dobos, Varvara Kanti, and Kathrin Hillmann
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medicine.medical_specialty ,Validation study ,Population ,Dermatology ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Quality of life ,Acne Vulgaris ,Humans ,Medicine ,030212 general & internal medicine ,Sensitivity to change ,Prospective cohort study ,education ,Acne ,education.field_of_study ,Adult female ,business.industry ,Dermatology Life Quality Index ,medicine.disease ,Surgery ,Infectious Diseases ,Face ,Quality of Life ,Female ,business - Abstract
Background The postadolescent form of acne papulopustulosa, also referred to as ‘acne tarda’ can have substantial negative impact on Quality of Life, especially in adult female patients. Objective Although the Dermatology Life Quality Index (DLQI) is widely used, empirical evidence about its performance in adult female acne patients is lacking. Methods In this prospective cohort study, we have investigated the sensitivity to change of the DLQI in 53 female adult acne patients with mild to moderate facial acne treated with azelaic acid (AzA) 15% gel twice daily over 24 weeks. Results Mean Investigator Static Global Assessment (ISGA) score was 2.3 (SD 0.5) at baseline and ranged from 0.9 (SD 0.3) to 2.1 (SD 0.4) at the end of the study in the ‘Highly Improved’ and ‘Unchanged’ responder groups respectively. The mean baseline DLQI score was 5.1 (SD 4.2). The Effect Size in the responder group ‘Highly Improved’ was 0.66; in group ‘Improved’ 0.62 and 0.23 in group ‘Unchanged’. At the end of study, the mean DLQI score ranged from 1.1 (SD 1.5) in the ‘Highly Improved’ group to 3.7 (SD 6.0) in the ‘Unchanged’ group. Conclusion The results support the sensitivity to change of the DLQI in this population.
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- 2016
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41. Épidémiologie globale des lymphomes cutanés primitifs : revue systématique et méta-analyse de 16 953 patients
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G. Dobos, Marisa Battistella, Anne Pohrt, Caroline Ram-Wolff, J.-D. Bouaziz, Martine Bagot, C. Lebbé, and D.M. Adèle
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Dermatology - Abstract
Introduction Les lymphomes cutanes primitifs sont un groupe heterogene de maladies rares. Plusieurs publications ont demontre des motifs epidemiologiques locaux, mais pour l’instant, il n’y avait pas encore de comparaison systematique globale publiee. Le but de cette etude etait de comparer les frequences relatives des lymphomes cutanes entre les differents pays du monde et d’analyser d’eventuels regroupements regionaux. Materiel et methodes Nous avons conduit une revue systematique de la litterature sur Medline (Pubmed) et dans la librairie Cochrane pour les publications incluant au moins 100 cas de lymphomes cutanes primitifs et au moins 3 diagnostics differents selon les classifications internationales reconnues. Les proportions relatives de chaque sous-type de lymphome cutane ont ete calculees et comparees dans une meta-analyse. Cette etude a ete realisee en accord avec son protocole enregistre et publie et avec les principes PRISMA. Resultats Apres une selection en double-aveugle, nous avons identifie 26 etudes rapportant 16 953 patients correspondant a nos criteres d’inclusion et exclusion. La frequence des lymphomes cutanes T etait 15 % plus elevee dans les populations asiatiques. La frequence moyenne du mycosis fongoide etait de 62 % avec une heterogeneite importante entre les etudes. Par contre, la frequence du syndrome de Sezary etait stable a 3 % independamment du pays. Certains lymphomes cutanes T rares, comme par exemple le lymphome T a type de panniculite ou le lymphome NK/T de type nasal, etaient plus frequents dans les etudes asiatiques. Discussion Cette meta-analyse globale des lymphomes cutanes a montre que les lymphomes cutanes T sont les lymphomes cutanes primitifs les plus frequents (83 % en moyenne) avec une predominance du mycosis fongoide. Cependant, la frequence relative du syndrome de Sezary etait plutot stable a environ 3 % ce qui pourrait indiquer qu’une instabilite genetique innee joue un role important dans la physiopathologie de cette maladie.
- Published
- 2020
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42. Analyse transcriptomique des fibroblastes dermiques associés aux lymphomes T cutanés : démonstration de leur rôle support
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G. Dobos, Jean-François Deleuze, Armand Bensussan, S. Peltier, Martine Bagot, Laurence Michel, Habib Zouali, S. Ly Ka So, Anne Boland, C. Battail, and Caroline Ram-Wolff
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Dermatology - Abstract
Introduction Le microenvironnement tissulaire joue un role cle dans l’oncogenese et favorise la croissance, l’invasion, les metastases et la resistance a la chimio-prevention des cellules tumorales. Notre objectif est de determiner quelle est la contribution du microenvironnement cutane mesenchymateux dans les lesions tumorales des lymphomes T cutanes (LTC) en caracterisant plus particulierement le profil d’expression genique des fibroblastes dermiques obtenus a partir de lesions cutanees. Materiel et methodes Un sequencage d’ARN (RNA-seq) a ete effectue sur des cultures primaires de fibroblastes cultives a partir de biopsies cutanees de 8 mycosis fongoides (MF), 6 syndrome de Sezary (SS) et 15 fibroblastes normaux (FN) provenant de plasties mammaires (âge apparie). Le RNA-seq a ete realise en utilisant les reactifs Illumina TruSeq V3. La quantification du niveau d’expression et l’identification des genes exprimes differentiellement (differential gene expression : DEG) dans les LTC par rapport aux temoins a ete realisee par DESeq2 (valeur de p ajustee padj Resultats 1044 DEG ont ete identifies entre les fibroblastes associes aux LTC et les FN, avec 542 genes sous-exprimes et 502 surexprimes (1345 genes dans les fibroblastes MF vs FN), 457 genes pour les SS et seulement 45 genes entre SS vs MF. L’analyse GSEA de tous les fibroblastes associes aux CTCL a identifie l’enrichissement de 3 voies principales de signalisation : “IFNa reponse”, “IFNγ reponse”,“cibles MYC”. L’analyse du facteur de transcription IPA® a mis en evidence 25 reseaux moleculaires et plusieurs ensembles de genes associes, dont « Inhibition des Metalloproteases » ou « Signalisation d’extravasation des leucocytes ». Les principaux genes d’interet ont ete valides en qRT-PCR. Discussion Les presentes donnees demontrent l’alteration de l’expression des genes dans les fibroblastes dermiques associes aux LTC, suggerant l’implication des cellules mesenchymateuses sur l’evolution des LTC.
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- 2020
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43. [Intra-arterial procaine injection in peripheral arterial disease]
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S, Schotes, F J, Saha, and G, Dobos
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Peripheral Arterial Disease ,Injections, Intra-Arterial ,Humans ,Pain ,Female ,Middle Aged ,Procaine ,Injections - Abstract
The report concerns a 61-year-old woman suffering from a chronic pain syndrome of peripheral arterial vascular disease. Despite level III-WHO medication she was not able to walk a distance of more than 100 m without pain. The patient received sonographically guided procaine injections into both femoral arteries. Directly after the injection the patient was free of pain for 4 weeks and for 6 months after a repeat injection.Wir berichten über eine 61-jährige Patientin, die unter einem Schmerzsyndrom bei pAVK leidet. Eine Gehstrecke von maximal 100 m war nur unter starken Schmerzen trotz WHO-Stufe-III-Medikation möglich. Die Patientin erhielt sonografisch gesteuerte intraarterielle Procaininjektionen in beide Femoralarterien. Nach der Injektion war die Patientin schmerzfrei für 4 Wochen und nach wiederholter Injektion 6 Monate.
- Published
- 2018
44. [Herbal medicines for psychiatric disorders]
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D, Anheyer, H, Haller, P, Klose, H, Cramer, and G, Dobos
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Depressive Disorder ,Depression ,Germany ,Herbal Medicine ,Mental Disorders ,Humans - Abstract
In Germany herbal medicines are traditionally frequently used. They represent an important therapeutic option, especially in self-medication.Current systematic review articles and meta-analyses were evaluated and summarized with respect to the evidence of phytotherapeutic drugs for selected psychiatric indications.Apart from the use of St. John's wort for depression, no other herb has so far shown convincing evidence.Due to the promising effects and the low side effect potential within the existing studies, further randomized controlled trials (e. g. for Passiflora incarnata, Rhodiola rosea and Lavendula officinalis) are definitely indicated.
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- 2018
45. Difficultés du diagnostic du lymphome T cutané anaplasique à grandes cellules CD30 positives
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Martine Bagot, Jean-David Bouaziz, G. Dobos, F. Herms, Pauline Brice, C. Lebbé, M.-V. Vignon-Pennamen, Jacqueline Rivet, Fanélie Jouenne, A. de Masson, Caroline Ram-Wolff, Marisa Battistella, J.-N. Dauendorffer, Samia Mourah, and Jean Michel Cayuela
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Dermatology - Abstract
Introduction Le lymphome T cutane anaplasique a grandes cellules est un lymphome T cutane (LTC) de bon pronostic avec expression de CD30 par plus de 75 % des cellules. Les lymphomes T cutanes primitifs qui ne correspondent a aucune des categories definies par la classification Organisation mondiale de la sante/European Organization for Research and Treatment of Cancer (OMS/EORTC) sont classes comme lymphome T peripherique non classable (pcPTCL-NOS). Materiel et methodes Nous presentons deux cas cliniques avec un diagnostic initial de pcPTCL-NOS avec peu ou pas d’expression de CD30 initiale qui echappaient apres la premiere ligne de traitement et rechutaient sous forme de lymphomes cutanes CD30+ avec une atteinte systemique. Observations Cas 1 : un patient de 79 ans presentait une plaque ulceree du prepuce. L’histologie montrait une infiltration dense de lymphocytes atypiques de taille moyenne sans epidermotropisme. Les cellules tumorales exprimaient CD3, CD8, granzyme B et 10 % etaient CD30+, ce qui permettait de porter le diagnostic de pcPTCL-NOS. Le patient etait en reponse complete apres radiotherapie. Il rechutait 4 ans plus tard sous forme de lesions cutanees et systemiques. L’examen anatomopathologique montrait un aspect de lymphome anaplasique a grandes cellules, avec une infiltration lymphocytaire dense, dont 80 % des cellules etaient CD30+. Les traitements par doxorubicine liposomale pegylee et brentuximab vedotin permettaient d’obtenir une reponse complete, mais le patient rechutait a nouveau. Une analyse des recepteurs T des lymphocytes par hightroughput sequencing retrouvait un clone T identique au diagnostic initial et au moment de la rechute dans les biopsies cutanees. Cas 2 : un patient de 71 ans se presentait avec des symptomes B et des ulcerations du genou droit. La biopsie montrait une infiltration dermique par des lymphocytes de taille moyenne, CD3+ CD5-, CD7-, granzyme B+, CD4+/− et CD8+/−, sans expression de CD30. La tomographie a emission de positons–tomodensitometrie (TEP-TDM) etait strictement normale, le diagnostic de pcPTCL-NOS etait retenu. Quelques mois apres la polychimiotherapie, le patient rechutait avec une atteinte systemique et des ulcerations cutanees. La biopsie montrait un aspect de lymphome T anaplasique CD30+. Discussion L’heterogeneite de l’expression du CD30 chez un meme patient et dans la meme biopsie a deja ete rapportee. Ces observations demontrent la plasticite d’un meme clone T qui peut realiser des tableaux anatomocliniques differents ce qui peut avoir des consequences therapeutiques, en particulier concernant les possibilites de traitement par un anticorps anti-CD30. Conclusion Il est toujours utile de faire plusieurs biopsies initiales et au cours de l’evolution devant des lymphomes cutanes de classement et de traitement difficiles.
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- 2019
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46. Evaluation of skin ageing: a systematic review of clinical scales
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Ulrike Blume-Peytavi, Jan Kottner, G. Dobos, and Andrea Lichterfeld
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Observer Variation ,Skin ageing ,medicine.medical_specialty ,business.industry ,media_common.quotation_subject ,Scopus ,MEDLINE ,Reproducibility of Results ,Dermatology ,Skin Aging ,Inter-rater reliability ,Scale (social sciences) ,Criterion validity ,medicine ,Health Status Indicators ,Humans ,Medical physics ,Quality (business) ,business ,Reliability (statistics) ,media_common - Abstract
Clinical scales are widely used in anti-ageing research and practice. More than 100 skin ageing scales exist, which makes it difficult to choose outcome measures and to compare study results. The objectives were to assess and evaluate the quality of measurement properties of available clinical skin ageing scales. A systematic review was conducted. Electronic databases including Medline (1970 to June 2013) and EMBASE (1974 to June 2013) were searched via Ovid SP. To enhance the sensitivity forward searches were conducted in Scopus and Web of Science. We identified 111 scales in 52 included publications. Thirty studies had good methodology for at least one measurement property. Forty-two scales were evaluated for their test-retest or interrater reliability. Nineteen showed high reliability coefficients. A further 15 instruments were partly supported by content and/or structural and/or criterion validity and/or hypotheses-testing evidence. The majority of existing clinical skin ageing scales were developed for evaluating facial characteristics. Many scales quantify similar constructs. In contrast to the high number of available scales there is limited evidence supporting their measurement properties. Recommendations for the use of specific skin ageing scales for clinical studies must be made with caution because of the high number of studies with poor methodology. Development of new instruments should be justified, and existing ones investigated for scale behaviour using appropriate methods. Future research should aim to select and/or adapt existing scales to identify the 'best' to improve clinical research and practice.
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- 2015
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47. Does dietary fluid intake affect skin hydration in healthy humans? A systematic literature review
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G. Dobos, Jan Kottner, Merve Akdeniz, Tsenka Tomova-Simitchieva, and Ulrike Blume-Peytavi
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Skin physiology ,Drinking ,Physiology ,Dermatology ,030207 dermatology & venereal diseases ,03 medical and health sciences ,Skin hydration ,0302 clinical medicine ,Body Water ,Skin Physiological Phenomena ,Dry skin ,medicine ,Stratum corneum ,Humans ,Skin ,Transepidermal water loss ,integumentary system ,business.industry ,Water ,Hydrogen-Ion Concentration ,Water Loss, Insensible ,Sebum ,Systematic review ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Dryness ,Observational study ,medicine.symptom ,Epidermis ,business - Abstract
Background Associations between daily amounts of drinking water and skin hydration and skin physiology receive increasingly attention in the daily life and in clinical practice. However, there is a lack of evidence of dermatological benefits from drinking increased amounts of water. Materials and methods Pubmed and Web of Science were searched without any restrictions of publication dates. References of included papers and related reviews were checked. Eligibility criteria were primary intervention and observational studies investigating the effects of fluid intake on skin properties in English, German, Spanish or Portuguese language, including subjects being healthy and 18+ years. Results Searches resulted in 216 records, 23 articles were read in full text, and six were included. The mean age of the samples ranged from 24 to 56 years. Overall the evidence is weak in terms of quantity and methodological quality. Disregarding the methodological limitations a slight increase in stratum corneum and "deep" skin hydration was observed after additional water intake, particularly in individuals with lower prior water consumption. Reductions of clinical signs of dryness and roughness were observed. The extensibility and elasticity of the skin increased slightly. Unclear associations were shown between water intake and transepidermal water loss, sebum content, and skin surface pH. Conclusions Additional dietary water intake may increase stratum corneum hydration. The underlying biological mechanism for this possible relationship is unknown. Whether this association also exists in aged subjects is unclear. Research is needed to answer the question whether increased fluid intake decreases signs of dry skin.
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- 2018
48. Intra-arterial procaine injection in peripheral arterial disease
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G. Dobos, S. Schotes, and F. J. Saha
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medicine.medical_specialty ,Neurology ,Sports medicine ,business.industry ,Pain medicine ,Chronic pain ,Medizin ,Psychosomatic medicine ,030208 emergency & critical care medicine ,medicine.disease ,Rheumatology ,Peripheral ,03 medical and health sciences ,Procaine ,0302 clinical medicine ,Anesthesiology and Pain Medicine ,Internal medicine ,Anesthesia ,medicine ,030212 general & internal medicine ,Neurology (clinical) ,business ,medicine.drug - Abstract
The report concerns a 61-year-old woman suffering from a chronic pain syndrome of peripheral arterial vascular disease. Despite level III-WHO medication she was not able to walk a distance of more than 100 m without pain. The patient received sonographically guided procaine injections into both femoral arteries. Directly after the injection the patient was free of pain for 4 weeks and for 6 months after a repeat injection.
- Published
- 2018
49. Evidence-based (S3) guideline for the treatment of androgenetic alopecia in women and in men - short version
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Alexander Nast, A. Finner, Anja Blumeyer, Pascal Reygagne, Myrto Trakatelli, V. Del Marmol, Ulrike Blume-Peytavi, Varvara Kanti, Antonella Tosti, Bianca Maria Piraccini, Andrew G. Messenger, G. Dobos, Kanti, V, Messenger, A, Dobos, G, Reygagne, P, Finner, A, Blumeyer, A, Trakatelli, M, Tosti, A, Del Marmol, V, Piraccini, Bm, Nast, A, and Blume-Peytavi, U.
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Male ,medicine.medical_specialty ,Evidence-based practice ,Vasodilator Agents ,Dermatology ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Pharmacotherapy ,5-alpha Reductase Inhibitors ,Quality of life ,Outcome Assessment, Health Care ,Medicine ,Humans ,Low-Level Light Therapy ,Androgenetic alopecia, therapy, finasteride, minoxidil, Laser, guidelines, baldness ,skin and connective tissue diseases ,Hair transplantation ,Evidence-Based Medicine ,integumentary system ,business.industry ,Platelet-Rich Plasma ,Finasteride ,Alopecia ,Guideline ,Evidence-based medicine ,Dutasteride ,medicine.disease ,Infectious Diseases ,Hair loss ,Minoxidil ,030220 oncology & carcinogenesis ,Practice Guidelines as Topic ,Drug Therapy, Combination ,Female ,business ,medicine.drug ,Hair - Abstract
Androgenetic alopecia is the most common hair loss disorder, affecting both men and women. Initial signs of androgenetic alopecia usually develop during teenage years leading to progressive hair loss with a pattern distribution. Moreover, its frequency increases with age and affects up to 80% Caucasian men and 42% of women. Patients afflicted with androgenetic alopecia may undergo significant impairment of quality of life. The European Dermatology Forum (EDF) initiated a project to develop evidence-based guidelines for the treatment of androgenetic alopecia. Based on a systematic literature research the efficacy of the currently available therapeutic options was assessed and therapeutic recommendations were passed in a consensus conference. The purpose of the guideline is to provide dermatologists with an evidence-based tool for choosing an efficacious and safe therapy for patients with androgenetic alopecia.
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- 2017
50. Challenges in the diagnosis of CD30+ anaplastic large-cell lymphoma
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Martine Bagot, J.-N. Dauendorffer, Samia Mourah, Jean Michel Cayuela, C. Lebbé, Marisa Battistella, Jacqueline Rivet, Pauline Brice, G. Dobos, Caroline Ram-Wolff, M.-D. Vignon-Pennamen, F. Herms, J.-D. Bouaziz, A. de Masson, and Fanélie Jouenne
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Cancer Research ,Oncology ,business.industry ,Cancer research ,Medicine ,CD30+ Anaplastic Large Cell Lymphoma ,business - Published
- 2019
- Full Text
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