20 results on '"Ozluk E"'
Search Results
2. Massive Perivillous Fibrin Deposition and Chronic Histiocytic Intervillositis of a Placenta: Rare co-existence
- Author
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Ozluk, E, primary, Cotelingam, J, additional, and Ong, M, additional
- Published
- 2020
- Full Text
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3. Extra-nodal Rosai-Dorfman Disease Confined to Breast
- Author
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Ozluk, E, primary and Shackelford, R, additional
- Published
- 2020
- Full Text
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4. Risk factors for delirium occurring after deep brain stimulation surgery in patients with Parkinson's disease.
- Author
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Ozluk E and Ozturk G
- Subjects
- Humans, Male, Female, Aged, Risk Factors, Middle Aged, Retrospective Studies, Subthalamic Nucleus surgery, Deep Brain Stimulation adverse effects, Deep Brain Stimulation methods, Parkinson Disease therapy, Parkinson Disease surgery, Delirium etiology, Postoperative Complications etiology, Postoperative Complications epidemiology
- Abstract
Objective: Postoperative delirium (POD) may cause cognitive morbidities and prolonged hospital stay. This study aimed to evaluate the risk factors associated with postoperative delirium in patients undergoing deep brain stimulation (DBS) for Parkinson's disease (PD)., Method: We retrospectively reviewed 83 patients with idiopathic PD who underwent bilateral DBS between 2016 and 2023. The target of DBS was the globus pallidus interna (Gpi) or the subthalamic nucleus (STN) in 84.3% and 15.7% of patients, respectively. Patients were evaluated using the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) and categorized into two groups: those with delirium and those without. Demographic features, disease duration, preoperative cognitive status (Mini-Mental State Examination) and silent ischemia, brain atrophy rates, DBS target location, surgical type and duration, Unified PD Rating Scale-3 scores, Hoehn and Yahr scores, postoperative perilead edema, and electrolyte imbalance were compared between patients with and without post-DBS delirium. Apart from univariate analysis, receiver operating characteristic (ROC) curve analysis for disease duration and multivariate logistic regression analyses were used to determine independent risk factors for post-DBS delirium., Results: Five out of the 83 patients (6%) developed post-DBS delirium. Age (> 68 years), disease duration, preoperative cerebral atrophy rates, and postoperative perilead edema were significantly higher in patients who developed delirium (p < 0.05 each). The ROC curve analysis revealed disease duration of ≥ 11 years as a risk factor for delirium (p = 0.001; odds ratio, OR: 58.4, 95% confidence interval, CI: 5.45-625.49). Age and disease duration were independent risk factors for post-DBS delirium (OR: 1.243, 95% CI: 1.070-1.592 and OR: 22.52, 95% CI: 1.21-383.96, respectively)., Conclusions: Older age and longer disease duration are independent risk factors for postoperative delirium in patients with PD. This study highlights the need to identify high-risk patients when undertaking DBS to facilitate early diagnosis and timely management., Competing Interests: Declarations. Ethical approval: This study was approved by our hospital’s ethics committee and conformed with the principles outlined in the Declaration of Helsinki. Competing interests: The authors declare no competing interests. Usage of AI in manuscript preparation: None., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)
- Published
- 2024
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5. Immune Reconstitution Inflammatory Syndrome in a Patient With Cutaneous Leishmaniasis and HIV: A Diagnostic Challenge for Clinicians Caring for a Migrant Population in the United States.
- Author
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De La Hoz A, Gadi N, Lopez CG, Barrera-Godinez A, Miller NS, Bourque DL, Brem C, Ozluk E, Seth G, Kimball S, and Taylor JL
- Abstract
Migration routes determine exposure to endemic infections. We present a case of complex cutaneous leishmaniasis in a man with HIV infection who migrated to the United States from Haiti, where Leishmania is uncommon, acquiring leishmaniasis while on his journey via South America and Central America. His presentation included hyperpigmented, nonulcerated plaques and nodules on his extremities, chest, back, face, palms, and soles; initially he had no mucosal lesions. Infection with Leishmania panamensis was confirmed via polymerase chain reaction. He was prescribed bictegravir/tenofovir alafenamide/emtricitabine with rapid suppression of HIV and liposomal amphotericin B for diffuse cutaneous leishmaniasis with a limited initial response. He subsequently developed mucosal lesions in the setting of immune reconstitution and was retreated with amphotericin dosed for mucocutaneous disease. A thorough migration history was critical to diagnosis. This case highlights the different presentations of leishmaniasis in people with HIV and the elevated risk for treatment failure., Competing Interests: Potential conflicts of interest. All authors: No reported conflicts., (© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.)
- Published
- 2024
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6. Quadruple Negative Metastatic Melanoma With Gain of SOX-11 Expression and TERT Mutation.
- Author
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Ozluk E, Lee J, and Wei EX
- Abstract
Malignant melanoma is a common and aggressive skin cancer with a high incidence of metastases. Diagnosis is usually straightforward, based on a combination of histomorphology and immunohistochemistry. However, metastatic melanoma is notorious for its phenotypic diversity and loss of differentiation markers. Through recent developments in diagnostic immunohistochemistry and molecular pathology, several new markers are identified to be of use in confirming melanoma diagnosis, especially in undifferentiated and dedifferentiated cases. Here we report a challenging case of a 59-year-old male with splenic metastatic melanoma which revealed a loss of four diagnostic melanocytic markers including S100, SOX-10, HMB45, and MART-1, but a gain of SOX-11., Competing Interests: Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work., (Copyright © 2024, Ozluk et al.)
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- 2024
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7. Multiple fibrotic lung nodules in a patient with primary Sjögren's syndrome.
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Carvajal-González A, Chennapragada SS, Ozluk E, and Morisetti P
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- Humans, Female, Middle Aged, Tomography, X-Ray Computed, Risk Factors, Inflammation, Lung diagnostic imaging, Sjogren's Syndrome complications, Sjogren's Syndrome diagnostic imaging
- Abstract
Evaluation of bilateral lung nodules noted on imaging poses a diagnostic challenge to clinicians as it can have many differentials from benign to malignant causes. It becomes especially critical to identify them right when there are underlying autoimmune conditions and risk factors for infection. However, a thorough investigation can lead to the recognition of rare associations as described below. We present here a 57-year-old woman who was admitted to the hospital with shortness of breath. Imaging with a computed tomography (CT) scan showed that she had 8 bilateral cystic pulmonary nodules with focal areas of ground-glass opacity and mediastinal lymphadenopathy. Fibrobronchoscopy and histopathological studies were done on the right middle lobe lung nodule demonstrated that the lung nodule was fibrotic with reactive inflammation but showed no malignant cells. Upon further detailed history and chart review, it was noted that the patient had a history of dry eyes leading to an autoimmune workup showing positive antinuclear antibodies (ANA), anti-Ro, and anti-La antibodies with no follow-up since then. This lead to the suspicion that these nodules could be related to underlying Sjögren's syndrome. Initial inpatient management with intravenous steroids showed significant improvement in her symptomatology. Hence, we present this rare association of lung nodules with Sjögren's syndrome and its management for awareness of this condition., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Inc.)
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- 2023
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8. A Case of Nonhealing Skin Ulcers in a Patient with Nonuremic Calciphylaxis.
- Author
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Agarwal S, Ozluk E, and Boparai S
- Abstract
Competing Interests: There are no conflicts of interest.
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- 2023
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9. A Rare Case of Pure Primary Large Cell Neuroendocrine Carcinoma of the Gallbladder.
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Shackelford RE, Ozluk E, Abdulsattar J, Lairmore TC, Chu Q, and Wei EX
- Abstract
Primary large cell neuroendocrine carcinoma (LCNEC) of the gallbladder is a rare malignancy which is often associated with non-LCNEC histologic components. Histologically "pure" LCNECs of the gallbladder are exceedingly rare with only 15 cases reported in the medical literature. Clinically, LCNECs present with abdominal pain and jaundice and follow an aggressive course with patients surviving a median of 15 months following initial diagnosis. To our knowledge, we present the 16
th case of a histologically pure LCNEC in a 62-year-old African American male who was successfully treated surgically. After discharge, he was subsequently lost to follow-up. Due to the extreme rarity of such disease entity, accurate diagnosis and proper management are essential for the best clinical outcome., Competing Interests: The authors declare that there is no conflict of interest regarding the publication of this article., (Copyright © 2022 Rodney E. Shackelford et al.)- Published
- 2022
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10. Ethylmalonic Encephalopathy 1 Protein Is Increased in Colorectal Adenocarcinoma.
- Author
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Ozluk E, Coppola D, Mohammad IZ, Islam T, Ghali G, Kevil CG, and Shackelford RE
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- Adenocarcinoma pathology, Colon metabolism, Colonic Neoplasms pathology, Humans, Neoplasm Staging, Adenocarcinoma metabolism, Colonic Neoplasms metabolism, Mitochondrial Proteins metabolism, Nucleocytoplasmic Transport Proteins metabolism
- Abstract
Background/aim: Ethylmalonic encephalopathy 1 protein (ETHE1) plays an important role in sulfide catabolism and polysulfide formation. As sulfides and polysulfides have recently been identified as playing important roles in cancer, we hypothesized that ETHE1 expression would be increased in colon cancer., Materials and Methods: We used tissue microarray analysis to compare ETHE1 expression in benign colonic epithelium compared to colonic adenocarcinoma. In total, 26 benign colonic epithelial samples were compared to 122 cases of colonic adenocarcinomas., Results: Compared to benign colonic epithelium, ETHE1 expression was significantly increased (~two-fold) in colonic adenocarcinoma. Additionally, this expression increased with increasing colon cancer tumor grades., Conclusion: ETHE1 expression is increased in colon cancer compared to benign colonic epithelium. These data, combined with previous studies, suggest that ETHE1 may contribute to colon carcinogenesis by promoting tumor cell bioenergetics and polysulfide formation., (Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
- Published
- 2021
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11. Primary Pulmonary Leiomyosarcoma in a Forty-Year-Old Woman.
- Author
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Ozluk E, Wei EX, Cotelingam J, and Shackelford RE
- Abstract
Primary pulmonary leiomyosarcomas (PPLs) are rare aggressive malignancies originating from the smooth muscle cells of the pulmonary interstitium, bronchial tree, or blood vessels. Accounting for <0.5% of lung tumors, PPLs are often initially undetected or misdiagnosed as pulmonary emboli, cardiac neoplasms, or as other more common lung cancer subtypes. Due to their aggressive and often lethal clinical profile, the diagnostic delay of PPL can significantly affect patient outcomes and must be avoided. Here we describe a case of PPL in a 40-year-old woman., Competing Interests: We report no conflicts of interests., (Copyright © 2021 by S. Karger AG, Basel.)
- Published
- 2021
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12. Cystathionine Gamma-Lyase Is Increased in Testicular Seminomas, Embryonal, and Yolk Sac Tumors.
- Author
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Ozluk E, Patel S, Coppola D, Ghali G, Cotelingam JD, Kevil CG, and Shackelford RE
- Subjects
- Case-Control Studies, Gene Expression Profiling methods, Gene Expression Regulation, Neoplastic, Humans, Male, Seminoma, Tissue Array Analysis, Carcinoma, Embryonal metabolism, Cystathionine gamma-Lyase metabolism, Endodermal Sinus Tumor metabolism, Testicular Neoplasms metabolism, Up-Regulation
- Abstract
Background: Testicular cancer constitutes 1.0% of male cancer and typically carries a good prognosis. As far as we are aware, the role for hydrogen sulfide in testicular cancer and the level of hydrogen sulfide-synthesizing enzyme have never been addressed. Here we examined cystathionine gamma-lyase (CSE) expression in several germ-cell testicular tumors., Materials and Methods: Tissue microarrays were employed to examine CSE expression in 32 benign testicular samples, 88 testicular seminomas, 34 embryonal carcinomas, 4 mature teratomas, and 16 yolk sac tumors, and CSE expression was compared to that seen in benign testicular tissue., Results: Compared to benign testicular tissue, CSE expression was increased in all three types of testicular neoplasm but not in mature teratomas. Highest CSE expression was identified in embryonal carcinomas, which often show a relatively aggressive clinical course., Conclusion: For the first time, we show that CSE is increased in several common testicular germ-cell tumor types., (Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
- Published
- 2021
- Full Text
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13. Hydrogen sulfide and DNA repair.
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Shackelford R, Ozluk E, Islam MZ, Hopper B, Meram A, Ghali G, and Kevil CG
- Subjects
- Animals, Ataxia Telangiectasia Mutated Proteins genetics, Ataxia Telangiectasia Mutated Proteins metabolism, Cell Cycle Proteins metabolism, DNA Damage, Humans, Phosphorylation, DNA Repair, Hydrogen Sulfide
- Abstract
Recent evidence has revealed that exposing cells to exogenous H 2 S or inhibiting cellular H 2 S synthesis can modulate cell cycle checkpoints, DNA damage and repair, and the expression of proteins involved in the maintenance of genomic stability, all suggesting that H 2 S plays an important role in the DNA damage response (DDR). Here we review the role of H 2 S in the DRR and maintenance of genomic stability. Treatment of various cell types with pharmacologic H 2 S donors or cellular H 2 S synthesis inhibitors modulate the G 1 checkpoint, inhibition of DNA synthesis, and cause p21, and p53 induction. Moreover, in some cell models H 2 S exposure induces PARP-1 and g-H2AX foci formation, increases PCNA, CHK2, Ku70, Ku80, and DNA polymerase-d protein expression, and maintains mitochondrial genomic stability. Our group has also revealed that H 2 S bioavailability and the ATR kinase regulate each other with ATR inhibition lowering cellular H 2 S concentrations, whereas intracellular H 2 S concentrations regulate ATR kinase activity via ATR serine 435 phosphorylation. In summary, these findings have many implications for the DDR, for cancer chemotherapy, and fundamental biochemical metabolic pathways involving H 2 S., (Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2021
- Full Text
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14. Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma.
- Author
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Dabrowski D, Ozluk E, Barbeito S, and Wei EX
- Abstract
Renal cell carcinoma (RCC) is the predominant renal malignancy in adults. Of the four general subtypes, papillary renal cell carcinoma (P-RCC) is the second most common and can be subdivided into type I, type II, and a mixture of type I and II. Focal segmental glomerulosclerosis (FSGS) is the most common glomerulopathy at all ages, and it can be seen as a paraneoplastic syndrome. RCC, in general, is known to present with many paraneoplastic syndromes, and glomerulopathies are among these. Rarely, RCC and glomerulopathies may overlap in the same patient. Here, we report a 58-year-old male with a past medical history of FSGS and chronic kidney disease (CKD), stage III, who was found to have an incidental renal mass that was later diagnosed as type II P-RCC. The histology showed pseudostratified tumor cells with an eosinophilic cytoplasm that formed papillary configurations and displayed areas of necrosis. The prior FSGS diagnosis exhibited segmental sclerosis, refractory tufts, and capillary membrane wrinkling. A period of 1.5 years elapsed between the diagnosis of the glomerulopathy and the malignancy. The tumor was found to be at stage TIb. To our knowledge, this may be the first reported case of usual-type FSGS as paraneoplastic glomerulopathy (PG) preceding P-RCC. Because FSGS only sparingly affects the kidney and is a common glomerulopathy in adults, it is reasonable to complete comprehensive diagnostic studies and commence medically necessary treatment, especially in the background of other renal comorbidities. These preexisting comorbidities may be associated with malignancy very early in its course. The probability of RCC-associated paraneoplastic glomerulopathy is low, which means an already incidentally found renal mass may conceal a serpentine paraneoplastic syndrome. A more developed understanding of these manifestations can lead experienced clinicians to suspect and possibly uncover an insidious RCC before it advances., Competing Interests: The authors declare that there is no conflict of interest regarding the publication of this paper., (Copyright © 2020 Dominik Dabrowski et al.)
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- 2020
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15. Brain MRI Findings in Patients in the Intensive Care Unit with COVID-19 Infection.
- Author
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Kandemirli SG, Dogan L, Sarikaya ZT, Kara S, Akinci C, Kaya D, Kaya Y, Yildirim D, Tuzuner F, Yildirim MS, Ozluk E, Gucyetmez B, Karaarslan E, Koyluoglu I, Demirel Kaya HS, Mammadov O, Kisa Ozdemir I, Afsar N, Citci Yalcinkaya B, Rasimoglu S, Guduk DE, Kedir Jima A, Ilksoz A, Ersoz V, Yonca Eren M, Celtik N, Arslan S, Korkmazer B, Dincer SS, Gulek E, Dikmen I, Yazici M, Unsal S, Ljama T, Demirel I, Ayyildiz A, Kesimci I, Bolsoy Deveci S, Tutuncu M, Kizilkilic O, Telci L, Zengin R, Dincer A, Akinci IO, and Kocer N
- Subjects
- Adult, Aged, Aged, 80 and over, Betacoronavirus isolation & purification, Brain pathology, Brain Diseases epidemiology, COVID-19, Comorbidity, Coronavirus Infections complications, Coronavirus Infections epidemiology, Coronavirus Infections pathology, Female, Humans, Intensive Care Units, Magnetic Resonance Imaging, Male, Middle Aged, Pandemics, Pneumonia, Viral complications, Pneumonia, Viral epidemiology, Pneumonia, Viral pathology, Retrospective Studies, SARS-CoV-2, Brain diagnostic imaging, Brain Diseases diagnostic imaging, Brain Diseases virology, Coronavirus Infections diagnostic imaging, Pneumonia, Viral diagnostic imaging
- Abstract
Online supplemental material is available for this article.
- Published
- 2020
- Full Text
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16. A Pregnant Woman with Cranial Aneurysm Rupture in the Second Trimester of Pregnancy.
- Author
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Karabuk E, Kadirogullari P, Kutlu Dilek TU, Ozluk E, and Ozturk G
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- Adult, Aneurysm, Ruptured diagnostic imaging, Angiography, Digital Subtraction, Female, Humans, Intracranial Aneurysm diagnostic imaging, Magnetic Resonance Imaging, Pregnancy, Pregnancy Complications, Cardiovascular diagnostic imaging, Pregnancy Trimester, Second, Surgical Instruments, Aneurysm, Ruptured surgery, Intracranial Aneurysm surgery, Pregnancy Complications, Cardiovascular surgery
- Abstract
Background: Reports of cerebral aneurysm and aneurysm rupture during pregnancy are rare in the literature. Aneurysms might rupture and cause intracranial hemorrhage during or after pregnancy. Aneurysmal subarachnoid hemorrhage during pregnancy presents a challenge regarding treatment and management. No institution has reported a large patient population or experience in managing this condition during pregnancy in the literature. Owing to the limited number of cases, there are no available treatment guidelines, and treatment is usually based on a case-by-case approach., Case Description: A 31-year-old woman presented in the 27th week of pregnancy with sudden-onset headache, which was diagnosed as subarachnoid hemorrhage. The diagnosis of subarachnoid hemorrhage with an aneurysm located on the anterior communicating artery was made with magnetic resonance imaging and digital subtraction angiography. The aneurysm was treated by surgical clipping. The pregnancy continued successfully until the 35th gestational week, when the infant was successfully delivered by planned cesarean section owing to preeclampsia and fetal growth retardation. Postoperative follow-up was uneventful., Conclusions: We present our experience in the management of aneurysmal subarachnoid hemorrhage during pregnancy and maternal and fetal outcomes of this rare disease. More cases and multicenter studies are needed to develop standardized management of this disease., (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Published
- 2020
- Full Text
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17. Quantitative susceptibility mapping in superficial hemosiderosis of the central nervous system.
- Author
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Dargazanli C, Deverdun J, Lionnet C, Michau S, Ozluk E, Corlobé A, Ayrignac X, Carra-Dallière C, Le Bars E, Labauge P, Bonafé A, and Menjot de Champfleur N
- Subjects
- Humans, Male, Young Adult, Brain diagnostic imaging, Brain Diseases diagnostic imaging, Cerebral Angiography methods, Hemosiderosis diagnostic imaging, Intracranial Hypertension diagnostic imaging, Magnetic Resonance Imaging methods
- Published
- 2015
- Full Text
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18. Histopathologic Study of Pathergy Test in Behçet's Disease.
- Author
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Ozluk E, Balta I, Akoguz O, Kalkan G, Astarci M, Akbay G, and Eksioglu M
- Abstract
Background: The pathergy test (PT) is important in the diagnosis of Behçet's disease (BD). However, misinterpretation of the test might cause false-positive or false-negative results. Therefore, immunopathologic and histopathologic tests are recommended with PT., Aims and Objectives: The aim of this study is to determine histopathologic findings of positive pathergy reaction at BD., Materials and Methods: This study was performed on 23 patients with BD. All patients were in active period of the disease. After 48 h from the injection, biopsy was performed on positive pathergy lesions., Results: Of the specimen from positive PT lesions of patients with BD, nine revealed mixed type inflammatory cell infiltration (39.1%), two revealed lobular panniculitis without vasculitis (8.7%), two revealed neutrophil rich infiltration (8.7%), and five revealed lymphocyte rich infiltration (21.7%) at the subcutaneous tissue. Mixed type inflammatory cell infiltration (43.4%), endothelial swelling and thickening (17.3%), erythrocyte extravasation (26.0%), perivascular cell infiltration (13.0%), lymphocytic vascular reaction (8.6%), lymphocytic vasculitis (13.0%), and leukocytoclastic vasculitis (21.7%) were detected in dermis by histopathologic examinations. There was no statistically significant difference between histopathologic findings and sex, family history, and systemic involvement except uveitis., Conclusion: This is an exceptional study since it is the first study that determines subcutaneous tissue findings of positive pathergy reaction in Behçet patients. In our study, uveitis was found to be statistically significant in the patients who had vasculitis in dermis. It can be a clue for prediction of disease severity and course. Further, studies that include wide number of patients will better illuminate the correlation between subcutaneous tissue findings and disease severity and clinical course.
- Published
- 2014
- Full Text
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19. Percutaneous sclerotherapy of peripheral venous malformations in pediatric patients.
- Author
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Gulsen F, Cantasdemir M, Solak S, Gulsen G, Ozluk E, and Numan F
- Subjects
- Adolescent, Child, Child, Preschool, Dose-Response Relationship, Drug, Female, Fluoroscopy, Follow-Up Studies, Humans, Injections, Intralesional, Lower Extremity blood supply, Male, Phlebography, Polidocanol, Retrospective Studies, Sclerosing Solutions administration & dosage, Tissue Adhesives, Treatment Outcome, Ultrasonography, Upper Extremity blood supply, Vascular Malformations diagnostic imaging, Polyethylene Glycols administration & dosage, Sclerotherapy methods, Vascular Malformations therapy, Veins abnormalities
- Abstract
Purpose: To report the efficacy of percutaneous puncture and sclerosis using polidocanol in the treatment of venous malformations (VMs) in pediatric patients., Patients/methods: Between March 2007 and February 2011, a series of 19 patients with VMs on the upper and lower extremities had undergone a total of 89 sessions of intralesional sclerotherapy using polidocanol. All the procedures were performed in an angiographic suite under general anesthesia in order to maintain sedation for facilitating the procedure. For each injection, approximately 1 ml of 2% polidocanol was injected for each centimeter of the diameter of the lesion, with a maximum of 6 ml. Injection of the sclerosant was guided by real-time sonography and fluoroscopy., Results: After the treatment, the symptoms completely resolved in four patients (21%). Clinical symptoms, such as bulging and pain were improved in 12 out of 19 patients (63%). They remained unchanged in three patients (16%). During the procedures, no major complications were encountered. The minor complications (65%) encountered were swelling and pain after treatment which were resolved by taking NSAID within a few days., Conclusion: In pediatric patients, sonographically guided percutaneous puncture and fluoroscopically guided sclerosis using 2% polidocanol is effective, less invasive and safe for the treatment of VMs, with a high success rate and minimal complications.
- Published
- 2011
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20. Endovascular stent-graft placement for ruptured dissecting aortic aneurysm in an adolescent patient with systemic lupus erythematosus: case report.
- Author
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Gulsen F, Cantasdemir M, Ozluk E, Arisoy N, and Numan F
- Subjects
- Adolescent, Aortic Rupture diagnosis, Emergency Medicine, Female, Humans, Tomography, X-Ray Computed, Treatment Outcome, Aortic Rupture complications, Aortic Rupture therapy, Blood Vessel Prosthesis Implantation, Lupus Erythematosus, Systemic complications, Stents
- Published
- 2011
- Full Text
- View/download PDF
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