28 results on '"Giselle Martins"'
Search Results
2. Use of dermoscopy in the diagnosis of temporal triangular alopecia
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Jullyene Gomes de Campos, Cláudia Marina Puga Barbosa Oliveira, Sandra Adolfina Reyes Romero, Ana Paula Klein, Patricia Bandeira de Melo Akel, and Giselle Martins Pinto
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Alopecia ,Dermoscopy ,Diagnosis ,Dermatology ,RL1-803 - Abstract
Temporal triangular alopecia, also referred as congenital triangular alopecia, is an uncommon dermatosis of unknown etiology. It is characterized by a non-scarring, circumscribed alopecia often located unilaterally in the frontotemporal region. It usually emerges at ages 2-9 years. Alopecia areata is the main differential diagnosis, especially in atypical cases. Dermoscopy is a noninvasive procedure that helps distinguish temporal triangular alopecia from aloepecia areata. Such procedure prevents invasive diagnostic methods as well as ineffective treatments.
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- 2015
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3. Classical Ehlers-Danlos syndrome: clinical, Histological and ultrastructural aspects Síndrome de Ehlers-Danlos clássica: aspectos clínicos, histológicos e ultraestruturais
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Eduardo de Barros Coelho Bicca, Fabiano Bonow de Almeida, Giselle Martins Pinto, Luis Antônio Suíta de Castro, and Hiram Larangeira de Almeida Jr
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Colágeno tipo V ,Microscopia eletrônica de transmissão ,Microscopia eletrônica de varredura ,Síndrome de Ehlers-Danlos ,Collagen type V ,Ehlers-Danlos syndrome ,Microscopy, electron, scanning ,Microscopy, electron, scanning transmission ,Dermatology ,RL1-803 - Abstract
A 12-year-old boy with difficulty in wound healing and scars of unusual appearance was examined. Thin, shiny and protruding skin, characterizing pseudotumoral lesions, was observed on his knees and elbows. Loose joints and increased skin elasticity were also observed. Light microscopy showed rare collagen bundles and loosely dispersed collagen fibers. Irregularly distributed elastic tissue was observed, and transmission electron microscopy revealed disorganized collagen fibers. In cross sections under high magnifications, fibers of varying diameters could be seen, as well as an irregular fiber outline. Scanning electron microscopy of the dermis showed disorganized collagen fibers, which were rarely arranged in bundles. Isolated and crossed-over fibers were also foundPaciente masculino de 12 anos relatou dificuldade em cicatrizar, seguido por cicatrizes de aspecto infrequente . A pele dos joelhos e cotovelos é fina, brilhante e protrusa, caracterizando pseudo- tumores. Além disso apresenta hiperelasticidade cutânea e articular. A microscopia óptica demonstrou raros feixes colágenos, as fibras colágenas encontram-se dispersas. O tecido elástico está presente e secundariamente irregular. A microscopia eletrônica de transmissão também observou fibras colágenas desorganizadas e com cortes transversais em grande aumento evidenciou diâmetros variados e contorno irregular das mesmas. A microscopia eletrônica de varredura da derme demonstrou raros feixes colágenos e fibras colágenas isoladas e entrecruzadas
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- 2011
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4. [Untitled]
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Renata Hubner Frainer, Luciana Boff de Abreu, Giselle Martins Pinto, André Vicente Esteves de Carvalho, and Luana Pizarro Meneghello
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Anormalidades congênitas ,Hipotricose ,Transtornos da visão ,Congenital abnormalities ,Hypotrichosis ,vision disorders ,Dermatology ,RL1-803 - Abstract
Congenital hypotrichosis and Stargardt macular dystrophy are rare autosomal recessive disorder of unk nown etiology respectively characterized by hair loss, macular degeneration and severe progressive vision reduc tion. There are few reports in the literature with this association. Studies show that the defective gene is on the chro mosome I6q22.1 and involve cadherin molecule in the pathogenesis. Early recognition of these disorders often starts with hair changes and should alert the dermatologist for an eye examination thereby avoiding more severe ocular defect.A hipotricose congênita e a distrofia macular de Stargardt são desordens autossômicas recessivas raras de etiologias desconhecidas, caracterizadas respectivamente pela perda de cabelos, degeneração macular e redução pro gressiva e grave da visão de forma precoce. Encontram-se pouquíssimos relatos na literatura com a associação de ambas. Há estudos que demonstram que o gene defeituoso dessas doenças encontra-se no cromossomo I6q22.1 e implicam a participação da molécula caderina na patogênese das mesmas. O reconhecimento precoce dessas desor dens muitas vezes inicia por alterações capilares e deve alertar o dermatologista para uma análise oftalmológica para como forma de se evitar alterações oculares mais graves.
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- 2013
5. Graham-Little Piccardi Lassueur Syndrome: case report Síndrome de Graham-Little Piccardi Lassueur: relato de caso
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Raquel Bissacotti Steglich, Renata Elise Tonoli, Giselle Martins Pinto, Fernanda Melo Müller, Isabelle Maffei Guarenti, and Ernani Siegmann Duvelius
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Alopecia ,Hipotricose ,Líquen plano ,Hypotrichosis ,Lichen planus ,Dermatology ,RL1-803 - Abstract
A 33-year-old woman presented with a 3-year history of progressive alopecia of the scalp. Past treatment with hydroxicloroquine did not show improvement. Physical examination revealed multiple areas of alopecia with atrophic aspect of the scalp, and axillary and pubic hypotrichosis. Dermoscopy showed hyperkeratosis and accentuation of follicular ostia. Anatomopathological examination revealed decrease in the number of hair follicles, upper perifollicular infiltrate and areas with fibrosis. The Piccardi-Lassueur-Graham-Little syndrome is a rare disorder, characterized by the triad of multifocal scarring alopecia of the scalp, keratotic follicular eruption and hypotrichosis of axillary and pubic regions. Management is a challenge and many medications tried have controversial results. We report a case of this rare syndrome which improved with corticoids.Mulher, 33 anos, apresenta quadro de alopecia progressiva do couro cabeludo há 3 anos. Tratamento com hidroxicloroquina há 12 meses, sem apresentar melhora. Ao exame físico exibe múltiplas áreas de alopecia cicatricial no couro cabeludo, além de hipotricose axilar e pubiana. A dermatoscopia evidencia hipercetose folicular e acentuação dos óstios foliculares. O exame anatomopatológico revela diminuição do número de folículos pilosos, infiltrado perifolicular e fibrose. A síndrome de Graham-Little Piccardi Lassueur é uma dermatose rara, caracterizada pela tríade de alopecia cicatricial multifocal do couro cabeludo, ceratose folicular disseminada e hipotricose das regiões axilares e pubianas. A terapêutica desta dermatose é um desafio, muitas medicações relatadas tem resultados controversos. Relatamos o caso desta síndrome rara que apresentou melhora com corticoterapia.
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- 2012
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6. Concordance between direct microscopy and fungical culture for the diagnostic of feet's onychomycosis Concordância entre o exame micológico direto e a cultura para fungos no diagnóstico das onicomicoses dos pés
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Paulo Ricardo Martins Souza, Gerson Vettorato, Giselle Martins Pinto, Rodrigo Pereira Duquia, Tais Guarienti Amaro, Hiram Laranjeira de Almeira Junior, and Juliano de Avelar Breunig
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Cultura ,Dermatomicoses ,Microscopia ,Onicomicose ,Culture ,Dermatomycoses ,Microscopy ,Onychomycosis ,Dermatology ,RL1-803 - Abstract
Prospective study compared the agreement between the direct microscopy and fungical culture from subungueal samples of the patients with clinical suspicion of feet's onychomycosis. The agreement occurred in 56.1% of the exams with dermatophytes, in 52.4% by others fungi and in 90.4% of the negative cases, 0,54 according to the Kappa`s test. In 39.3% of the onychomycosis caused by dermatophytes and 31.8% by nondermatophytes, these were identificated only for direct microscopy. The direct microscopic showed more sensibility compared with the culture, being superior in 19.5% of the total sample and maintaining agreement with the culture in 71.5% of the sample.Estudo prospectivo avaliando a concordância entre os resultados do exame micológico direto e dacultura para fungos de material coletado de pacientes com suspeita clínica de onicomicose dos pés. Ocorreu concordância em 56,1% dos exames com dermatófitos, em 52,4% dos exames com outros fungos e em 90,4% dos exames negativos (0,54 de acordo com o teste kappa). Em 39,3% das onicomicoses por dermatófitos e em 31,8% das por não dermatófitos, os agentes etiológicos foram identificados somente pelo exame direto. O exame direto demonstrou maior sensibilidade, comparado ao cultural, sendo superior em 19,5% da amostra total e mantendo concordância com a cultura em 71,5% da amostra.
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- 2012
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7. A pilot retrospective study on trichoscopy of 21 cases of rosacea of the scalp
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Deborah, Lin, Giselle, Martins, Jessika, Sanz, Ludmila, Corral, and Mariya, Miteva
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Dermatology - Published
- 2023
8. Frontal fibrosing alopecia associated with lichen planus pigmentosus: A multicentre retrospective descriptive analytical study of 104 patients
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Flavia Oliveira Xavier de Brito, Rita Fernanda Cortez de Almeida, Carla Jorge Machado, Luciana Rodino Lemes, Andre Luiz Vairo Donda, Aline Blanco, Aline Lucy Galavotti Silveira, Andreia Munck, Caren dos Santos Lima, Carolina Porto Cotrim Canela, Carolina Oliveira Costa Fechine, Daniel Lago Obadia, Giselle Martins Pinto, Lorena Dourado Alves, Maria Fernanda Reis Gavazzoni Dias, Marcela Benez, Marcelo Rigatti, Nadia El Kadi, Priscila Kakizaki, Renan Minotto, Sidney Frattini, Paulo Müller Ramos, and Daniel Fernandes Melo
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Infectious Diseases ,Dermatology - Published
- 2023
9. Guidelines for clinical trials of frontal fibrosing alopecia: consensus recommendations from the International FFA Cooperative Group (IFFACG)*
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Wilma F. Bergfeld, Maria K. Hordinsky, S. Papanikou, Giselle Martins Pinto, Isabella Doche, Satoshi Itami, S. Malakar, K. Khobzei, Elise A. Olsen, Paradi Mirmirani, T. Silyuk, V. Chasapi, Rod Sinclair, Valerie D. Callender, Amy J. McMichael, Kenneth Washenik, Matthew Harries, R. O. Soares, Rodrigo Pirmez, N. Enechukwu, Lidia Rudnicka, Ulrike Blume-Peytavi, Won Soo Lee, Abraham Zlotogorski, Pascal Reygagne, David Saceda-Corralo, Yuliya Ovcharenko, Jerry Shapiro, A. Souissi, George Cotsarelis, Ramon Grimalt, O. Correia, Antonella Tosti, Douglas Canfield, Ncoza C. Dlova, Sergio Vano-Galvan, Annika Vogt, Rachita Dhurat, Andrew G. Messenger, Bianca Maria Piraccini, Janet L. Roberts, Olsen E.A., Harries M., Tosti A., Bergfeld W., Blume-Peytavi U., Callender V., Chasapi V., Correia O., Cotsarelis G., Dhurat R., Dlova N., Doche I., Enechukwu N., Grimalt R., Itami S., Hordinsky M., Khobzei K., Lee W.S., Malakar S., Messenger A., McMichael A., Mirmirani P., Ovcharenko Y., Papanikou S., Pinto G.M., Piraccini B.M., Pirmez R., Reygagne P., Roberts J., Rudnicka L., Saceda-Corralo D., Shapiro J., Silyuk T., Sinclair R., Soares R.O., Souissi A., Vogt A., Washenik K., Zlotogorski A., Canfield D., and Vano-Galvan S.
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Frontal fibrosing alopecia, group of experts in hair loss, consensus recommendations for clinical trials ,Clinical Trials as Topic ,medicine.medical_specialty ,Consensus ,Scalp ,business.industry ,Frontal fibrosing alopecia ,Lichen Planus ,MEDLINE ,Alopecia ,Guidelines as Topic ,Dermatology ,Scarring alopecia ,Patient assessment ,medicine.disease ,Clinical trial ,Cicatrix ,Hair loss ,medicine ,Etiology ,Humans ,Cooperative group ,business ,Intensive care medicine - Abstract
Background Frontal fibrosing alopecia (FFA) has become one of the most common causes of cicatricial alopecia worldwide. However, there is a lack of clear aetiology and robust clinical trial evidence for the efficacy and safety of agents currently used for treatment. Objectives To enable data to be collected worldwide on FFA using common criteria and assessment methods. Methods A multicentre, international group of experts in hair loss was convened by email to create consensus recommendations for clinical trials. Consensus was defined at > 90% agreement on each recommended part of these guidelines. Results Standardized diagnostic criteria, severity rating, staging, and investigator and patient assessment of scalp hair loss and other clinical features of FFA were created. Conclusions These guidelines should allow the collection of reliable aggregate data on FFA and advance efforts in both clinical and basic research to close knowledge gaps in this condition.
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- 2021
10. Straight to the Point: What Do We Know So Far on Hair Straightening?
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Simone Carolina Frattini, Patricia Damasco, Daniel Fernandes Melo, Giselle Martins Pinto, Flavia Weffort, and Taynara de Mattos Barreto
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integumentary system ,Point (typography) ,Computer science ,business.industry ,Internet privacy ,otorhinolaryngologic diseases ,sense organs ,Review Article ,Dermatology ,Hair straightening ,business - Abstract
Background: Hair represents a valued aspect of human individuality. The possibility of having an easy to handle hairstyle and changing it from time to time promoted an increasing search for chemical hair transformations, including hair straightening. Hair straightening is the process used to convert curly into straight hair. Aims: This review aims to discuss hair straightening, addressing techniques, products, methods of application, consequences to hair shafts, recommendations on this topic, and the risks involving the safety of both the user and the performing professional. Methods and Results: The terms “straightening” AND “hair,” “straightening” AND “alopecia,” and “straightening” AND “human hair” were used to perform a literature search in MEDLINE through PubMed until July 15, 2020. We limited the search to articles available in English, considering those mentioning alternatives to straighten the hair. We had a total of 33 relevant articles. Conclusions: This article will help dermatologists to advise their patients, providing a more suitable orientation on how to get the best outcome without risking one’s safety.
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- 2021
11. Permanent hair wavings: What dermatologists should know?
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Simone Carolina Frattini, Patricia Damasco, Giselle Martins Pinto, Flavia Weffort, Taynara de Mattos Barreto, and Daniel Fernandes Melo
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Administration, Topical ,Hair breakage ,Internet privacy ,Hair Preparations ,Dermatology ,Scarring alopecia ,Hair treatment ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,medicine ,Humans ,Oral toxicity ,Hair Cosmetics ,integumentary system ,business.industry ,Alopecia ,medicine.disease ,Curly hair ,Skin irritation ,030220 oncology & carcinogenesis ,sense organs ,Psychology ,business ,Dermatologists ,Hair - Abstract
Hair represents an important aspect of human individuality. The possibility of having an easy to handle hairstyle and changing it from time to time promoted an increasing search for chemical hair transformations, including permanent wavings (PW). PW is the chemical process used to convert straight into curly hair. Significant findings have been made in this field within the last three decades. In the past few years, PW has come back up to date, helping to define curls in wavy and curly hair and to create waves in straight hair. "Afro permanent" and "Beach waves" are some popular names for these new uses of PW. The primary safety concerns for PW generally arise from misuse or failure to comply with the product's usage instructions. Skin irritation, hair breakage, oral toxicity, sensitization, and scarring alopecia have been reported in the literature. Therefore, dermatologists need to understand well this matter to properly advise patients on how to get the best outcome without hazards. This review aims to discuss the main types of reducing agents used, the different techniques, the consequences to hair shafts, and the most important patients' recommendations on this topic.
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- 2020
12. Dissecting cellulitis in women: a retrospective multicenter study with 17 patients
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Daniel Fernandes Melo, Paulo Müller Ramos, Carla Jorge Machado, Alessandra Anzai, Aline Blanco, Fabiane Mulinari‐Brenner, Giselle Martins Pinto, Leonardo Spagnol Abraham, Lorena Dourado Alves, Marcelo Rigatti, Maria Cecilia Rivitti‐Machado, Priscila Kakizaki, Renan Minotto, Thalita Barbosa Macedo, Thuany Silva Santos, and Isabella Doche
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Scalp Dermatoses ,Humans ,Skin Diseases, Genetic ,Cellulitis ,Female ,Dermatology ,Retrospective Studies - Published
- 2022
13. Trichoscopy in Hair Restoration Practice: An Introduction for Hair Restoration Surgeons and Pathologists *
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Giselle Martins and Rui Oliveira Soares
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medicine.medical_specialty ,business.industry ,Medicine ,business ,Dermatology ,Trichoscopy - Published
- 2021
14. Risk factors for frontal fibrosing alopecia: A case-control study in a multiracial population
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Paulo Müller Ramos, Leopoldo Duailibe Nogueira Santos, Bruna Duque-Estrada, Fabiane Mulinari-Brenner, Giselle Martins Pinto, Rodrigo Pirmez, Débora Cadore de Farias, Hélio Amante Miot, Alessandra Anzai, Leonardo Spagnol Abraham, Daniel Fernandes Melo, Universidade Estadual Paulista (UNESP), Universidade de São Paulo (USP), Santa Casa de Misericórdia do Rio de Janeiro, Universidade Federal de Santa Catarina (UFSC), Universidade Estadual do Rio de Janeiro, Universidade Federal do Paraná (UFPR), Santa Casa Misericórdia, Universidade de Brasília (UnB), and Santa Casa de São Paulo
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medicine.medical_specialty ,Population ,frontal fibrosing alopecia ,Dermatology ,tobacco ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Recall bias ,medicine ,sunscreens ,risk factors ,Hair straightening ,education ,education.field_of_study ,integumentary system ,business.industry ,Frontal fibrosing alopecia ,Case-control study ,Environmental exposure ,Odds ratio ,medicine.disease ,Rosacea ,030220 oncology & carcinogenesis ,business ,case-control - Abstract
Made available in DSpace on 2022-05-01T03:29:53Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-03-01 Background: Frontal fibrosing alopecia (FFA) is a chronic cicatricial alopecia with unknown etiology and a worldwide rising incidence. Objective: The objective of this study was to evaluate the association of FFA with demographic and exposure factors in a Brazilian multiracial population. Methods: A multicenter case-control study was conducted in 11 referral centers throughout Brazil. The study was a case-control study that prospectively recruited 902 participants (451 patients with FFA and 451 sex-matched control individuals). Study participants completed a thorough questionnaire comprising variables grouped as baseline demographics, environmental exposure, diet, hormonal factors, allergies, and hair and skin care. Results: When adjusted by sex, age, menopause, and skin color, FFA was associated with hair straightening with formalin (odds ratio [OR], 3.18), use of ordinary (nondermatologic) facial soap (OR, 2.09) and facial moisturizer (OR, 1.99), thyroid disorders (OR, 1.69), and rosacea (OR, 2.08). Smokers (OR, 0.33) and users of antiresidue/clarifying shampoo (OR, 0.35) presented a negative association with FFA. There was no association with the use of sunscreen. Limitations: Recall bias. Conclusions: The association with moisturizers, ordinary facial soap, and hair straightening with formalin and the negative association with antiresidue/clarifying shampoo reinforce the possibility of an exogenous particle triggering FFA. Universidade Estadual Paulista Universidade de São Paulo Santa Casa de Misericórdia do Rio de Janeiro Universidade Federal de Santa Catarina Universidade Estadual do Rio de Janeiro Universidade Federal do Paraná Santa Casa Misericórdia Universidade de Brasília Santa Casa de São Paulo Universidade Estadual Paulista
- Published
- 2021
15. Regarding methodologic concerns in clinical studies on frontal fibrosing alopecia
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Rodrigo Pirmez, Giselle Martins Pinto, Hélio Amante Miot, Leopoldo Duailibe Nogueira Santos, Daniel Fernandes Melo, Débora Cadore de Farias, Bruna Duque-Estrada, Paulo Müller Ramos, Fabiane Mulinari-Brenner, Leonardo Spagnol Abraham, and Alessandra Anzai
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medicine.medical_specialty ,business.industry ,Frontal fibrosing alopecia ,MEDLINE ,Lichen Planus ,Medicine ,Humans ,Alopecia ,Dermatology ,business ,medicine.disease - Published
- 2020
16. Hair and Scalp Infections
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Mariya Miteva and Giselle Martins
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medicine.medical_specialty ,medicine.anatomical_structure ,business.industry ,Scalp ,medicine ,business ,Dermatology - Published
- 2019
17. Frequency of the Types of Alopecia at Twenty-Two Specialist Hair Clinics: A Multicenter Study
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Jose Cucchía, Antonella Tosti, Rodney Sinclair, Daniela Araucaria Guzmán-Sánchez, Jorge Larrondo, Susan Holmes, Ulrike Blume-Peytavi, Lidia Rudnicka, Ncoza C. Dlova, Daniel de la Rosa Carrillo, Bianca Maria Piraccini, David Saceda-Corralo, Sergio Vano-Galvan, Anisa Mosam, Ralph M. Trüeb, Jerry Shapiro, Ramon Grimalt, Maria Fernanda Reis Gavazzoni Dias, Annika Vogt, Matthew Harries, Rui Oliveira-Soares, Giselle Martins Pinto, Mariya Miteva, Rodrigo Pirmez, Anthony Ho, and Vañó-Galván S, Saceda-Corralo D, Blume-Peytavi U, Cucchía J, Dlova NC, Gavazzoni Dias MFR, Grimalt R, Guzmán-Sánchez D, Harries M, Ho A, Holmes S, Larrondo J, Mosam A, Oliveira-Soares R, Pinto GM, Piraccini BM, Pirmez R, De la Rosa Carrillo D, Rudnicka L, Shapiro J, Sinclair R, Tosti A, Trüeb RM, Vogt A, Miteva M.
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Central centrifugal cicatricial alopecia ,medicine.medical_specialty ,Traction alopecia ,Epidemiology ,Alopecia areata ,Dermatology ,Frontal fibrosing alopecia ,Telogen effluvium ,medicine ,skin and connective tissue diseases ,Androgenetic alopecia ,Lichen planopilaris ,integumentary system ,business.industry ,Acne keloidalis nuchae ,Folliculitis decalvan ,Hair disease ,Alopecia ,medicine.disease ,body regions ,stomatognathic diseases ,Lichen planopilari ,Hair diseases ,business ,Folliculitis decalvans ,600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit ,Research Article - Abstract
Background: The frequency of different types of alopecia is not clearly reported in recent studies. Objective: To analyze the frequency of the types of alopecia in patients consulting at specialist hair clinics (SHC) and to assess for global variations. Methods: Multicenter retrospective study including data from patients evaluated at referral SHC in Europe, America, Africa and Australia. Results: A total of 2,835 patients (72.7% females and 27.3% males) with 3,133 diagnoses of alopecia were included (73% were non-cicatricial and 27% were cicatricial alopecias). In all, 57 different types of alopecia were characterized. The most frequent type was androgenetic alopecia (AGA) (37.7%), followed by alopecia areata (AA) (18.2%), telogen effluvium (TE) (11.3%), frontal fibrosing alopecia (FFA) (10.8%), lichen planopilaris (LPP) (7.6%), folliculitis decalvans (FD) (2.8%), discoid lupus (1.9%) and fibrosing alopecia in a pattern distribution (FAPD) (1.8%). There was a male predominance in patients with acne keloidalis nuchae, dissecting cellulitis and FD, and female predominance in traction alopecia, central centrifugal cicatricial alopecia, FFA, TE, FAPD and LPP. Conclusion: AGA followed by AA and TE were the most frequent cause of non-cicatricial alopecia, while FFA was the most frequent cause of cicatricial alopecia in all studied geographical areas.
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- 2019
18. Contents Vol. 2, 2016
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Vidhi V. Shah, Tudor Pinteala, Stephanie Mlacker, Giulia Rech, Richard K. Scher, Luca Muscardin, Nilton Gioia Di Chiacchio, Shari Lipner, Dimitrios Rigopoulos, Robert Baran, Sema Aytekin, Nilton Di Chiacchio, Amanda Artis, Mariya I. Miteva, Mengensatzproduktion, Luiza Alonso Pereira, Adam S. Aldahan, Michelangelo La Placa, Claudio Marasca, Norma Cameli, Celso Tavares Sodré, Anca Eduard Chiriac, Dimitra Lianou, Evangelia Bozi, Giselle Martins Pinto, Emre Kaynak, Manasmon Chairatchaneeboon, Şirin Yaşar, Leandro Damiani, Giuseppe Monfrecola, Shari R. Lipner, Konstantina Diamanti, Francesca Larese Filon, Vasileia Damaskou, Paraskevi-Aikaterini Pierrakou, George Aravanis, Irina Rosca, Adam I. Rubin, Adina Coroaba, Damia L. Vendramini, Pierre Halteh, Raymond Fertig, Ramon Grimalt, Dimitris Rigopoulos, Elisa Raquel Martins da Costa Marques, Leandro Noriega, Dimitrios Sgouros, Slimane Zerdoud, Dimitra Daskari, Ioannis Panayiotides, Matteo Megna, Maria Mariano, Bruno R.L. Silveira, Maria Fernanda Reis Gavazzoni-Dias, Richard Scher, Jean-Pierre Delord, Ana Letícia Boff, Gabriella Fabbrocini, Vincent M. Hsu, Jhessica Andrade, Cristian Podoleanu, Fernanda Musa Aguiar, Aikaterini I. Liakou, Rodrigo Pirmez, Flávia Cury Rezende, Marcelo Teixeira, Miruna Negulescu, Zafer Küçükodacı, Pembegül Güneş, Mariana Vale Scribel da Silva, Druckerei Stückle, Emilie Tournier, Simona Stolnicu, Claudia Cavallotti, Antonella Tosti, Serge Boulinguez, Carlo Renè Girardelli, Vincent Sibaud, Lucy L. Chen, Jon Holmes, Maíra Rochael, Riccardo Balestri, Efstathios Rallis, Fatih Göktay, Alexandros C. Katoulis, Jessica S. Haber, Raymond M. Fertig, Bruna Duque-Estrada, Mariana Pinteala, Bianca Maria Piraccini, Antigoni Alevizou, Marius Florin Coros, Jerry Shapiro, Cynthia Magro, Letícia Arsie Contin, Chariklia Spiliadi, Wilma Bergfeld, Anca Chiriac, and Keyvan Nouri
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Dermatology - Published
- 2016
19. Dermoscopic Findings of Scalp Aplasia Cutis Congenita
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Giselle Martins Pinto, Mariana Vale Scribel da Silva, Fernanda Musa Aguiar, Leandro Damiani, and Mariya Miteva
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Hypertrichosis ,Pathology ,medicine.medical_specialty ,business.industry ,Dermatology ,medicine.disease ,Aplasia cutis congenita ,medicine.anatomical_structure ,Scalp ,medicine ,Nevus ,Original Article ,medicine.symptom ,Scalp aplasia cutis congenita ,business ,Aplasia cutis ,Rare disease - Abstract
Aplasia cutis congenita (ACC) is a rare disease characterized by congenital absence of skin, affecting preferentially the scalp. Diagnosis is made clinically; however, recent studies have shown that dermoscopy can be a useful tool for the diagnosis and differentiation from sebaceous nevus. The clinical findings include a shiny atrophic alopecic patch associated with dermoscopic findings of absent follicular openings, thicker vessels and a distinct collar hypertrichosis. We report 2 cases of alopecia presenting from birth. At dermoscopy, the absence of follicular openings and the increase in the caliber of vessels led us to establish the diagnosis of ACC.
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- 2016
20. It's not all traction: the pseudo ‘fringe sign’ in frontal fibrosing alopecia
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Rodrigo Pirmez, Yanna Kelly, Bruna Duque-Estrada, D.C. de Farias, Isabella Doche, Giselle Martins Pinto, and Leonardo Spagnol Abraham
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Adult ,Male ,medicine.medical_specialty ,business.industry ,medicine.medical_treatment ,Frontal fibrosing alopecia ,Alopecia ,Dermatology ,Middle Aged ,Traction (orthopedics) ,medicine.disease ,medicine.anatomical_structure ,Scalp Dermatoses ,Forehead ,medicine ,Humans ,Female ,business ,Aged ,Retrospective Studies - Published
- 2015
21. Use of dermoscopy in the diagnosis of temporal triangular alopecia
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Giselle Martins Pinto, Patrícia Bandeira de Melo Akel, Sandra Adolfina Reyes Romero, Cláudia Marina Puga Barbosa Oliveira, Jullyene Gomes de Campos, and Ana Paula Klein
- Subjects
Triangular alopecia ,Pathology ,medicine.medical_specialty ,Diagnostic methods ,Alopecia Areata ,Dermoscopy ,Dermatology ,Diagnosis, Differential ,Diagnosis ,Humans ,Medicine ,Imaging in Dermatology ,skin and connective tissue diseases ,integumentary system ,business.industry ,Infant ,Reproducibility of Results ,Alopecia ,Genetic Diseases, X-Linked ,Alopecia areata ,medicine.disease ,stomatognathic diseases ,RL1-803 ,Etiology ,Circumscribed alopecia ,Female ,Differential diagnosis ,business - Abstract
Temporal triangular alopecia, also referred as congenital triangular alopecia, is an uncommon dermatosis of unknown etiology. It is characterized by a non-scarring, circumscribed alopecia often located unilaterally in the frontotemporal region. It usually emerges at ages 2-9 years. Alopecia areata is the main differential diagnosis, especially in atypical cases. Dermoscopy is a noninvasive procedure that helps distinguish temporal triangular alopecia from aloepecia areata. Such procedure prevents invasive diagnostic methods as well as ineffective treatments.
- Published
- 2015
22. HTLV-1-associated infective dermatitis and probable HTLV-1- associated myelopathy in an adolescent female
- Author
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Giselle Martins Pinto, Renata Elise Tonoli, Paulo Ricardo Martins Souza, Rudimar dos Santos Riesgo, and Raquel Bissacotti Steglich
- Subjects
Doenças desmielinizantes ,Adolescent ,viruses ,Case Report ,Dermatite ,Dermatitis ,Dermatology ,Myelopathy ,immune system diseases ,hemic and lymphatic diseases ,Tropical spastic paraparesis ,Spastic ,Medicine ,Humans ,In patient ,Human T cell lymphotropic virus type 1 ,Vírus Linfotrópico T Tipo 1 Humano ,Human T-lymphotropic virus 1 ,biology ,business.industry ,virus diseases ,HTLV 1-associated myelopathy ,Paraparesis, tropical spastic ,biology.organism_classification ,medicine.disease ,HTLV-I Infections ,Immunohistochemistry ,Demyelinating diseases ,Scalp Dermatoses ,RL1-803 ,Infective dermatitis ,Immunology ,Skin Diseases, Viral ,Disease Progression ,Paraparesia espástica tropical ,Female ,business - Abstract
Human T cell lymphotropic virus type 1 (HTLV-1)-associated infective dermatitis (ID) is a chronic, severe and recurrent eczema occurring during childhood in patients vertically infected with HTLV-1. HTLV-1-associated myelopathy/tropical spastic paraparesia (HAM/ TSP) is slow and progressive. We report the case of an adolescent female from a non-endemic area for HTLV-1 who presents ID and, most likely, associated HAM/TSP.
- Published
- 2015
23. Graham-Little Piccardi Lassueur Syndrome: case report
- Author
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Ernani Siegmann Duvelius, Renata Elise Tonoli, Giselle Martins Pinto, Raquel Bissacotti Steglich, Fernanda Melo Müller, and Isabelle Maffei Guarenti
- Subjects
Adult ,medicine.medical_specialty ,Pathology ,Hyperkeratosis ,Dermoscopy ,Physical examination ,Dermatology ,Scarring alopecia ,Hypotrichosis ,Cicatrix ,medicine ,Humans ,Rare syndrome ,Scalp ,integumentary system ,medicine.diagnostic_test ,business.industry ,Alopecia ,Keratosis ,Syndrome ,Progressive alopecia ,medicine.disease ,body regions ,medicine.anatomical_structure ,Female ,Graham Little Piccardi Lassueur syndrome ,business - Abstract
A 33-year-old woman presented with a 3-year history of progressive alopecia of the scalp. Past treatment with hydroxicloroquine did not show improvement. Physical examination revealed multiple areas of alopecia with atrophic aspect of the scalp, and axillary and pubic hypotrichosis. Dermoscopy showed hyperkeratosis and accentuation of follicular ostia. Anatomopathological examination revealed decrease in the number of hair follicles, upper perifollicular infiltrate and areas with fibrosis. The Piccardi-Lassueur-Graham-Little syndrome is a rare disorder, characterized by the triad of multifocal scarring alopecia of the scalp, keratotic follicular eruption and hypotrichosis of axillary and pubic regions. Management is a challenge and many medications tried have controversial results. We report a case of this rare syndrome which improved with corticoids.
- Published
- 2012
24. Concordance between direct microscopy and fungical culture for the diagnostic of feet's onychomycosis
- Author
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Rodrigo Pereira Duquia, Gerson Vettorato, Juliano de Avelar Breunig, Paulo Ricardo Martins Souza, Giselle Martins Pinto, Hiram Laranjeira de Almeira Junior, and Tais Guarienti Amaro
- Subjects
Foot Dermatoses ,Microscopy ,medicine.medical_specialty ,business.industry ,Arthrodermataceae ,Concordance ,education ,Direct microscopy ,Dermatology ,Surgery ,Predictive Value of Tests ,Onychomycosis ,medicine ,Dermatomycoses ,Humans ,Prospective Studies ,business - Abstract
Prospective study compared the agreement between the direct microscopy and fungical culture from subungueal samples of the patients with clinical suspicion of feet's onychomycosis. The agreement occurred in 56.1% of the exams with dermatophytes, in 52.4% by others fungi and in 90.4% of the negative cases, 0,54 according to the Kappa`s test. In 39.3% of the onychomycosis caused by dermatophytes and 31.8% by nondermatophytes, these were identificated only for direct microscopy. The direct microscopic showed more sensibility compared with the culture, being superior in 19.5% of the total sample and maintaining agreement with the culture in 71.5% of the sample.
- Published
- 2012
25. Three simultaneous paraneoplastic manifestations (ichthyosis acquisita, Bazex syndrome, and Leser–Trélat sign) with prostate adenocarcinoma
- Author
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Juliana Steckel Bortoluzzi, Ana Cecília Michel Rosa, Rodrigo Pereira Duquia, Hiram Larangeira de Almeida, and Giselle Martins Pinto
- Subjects
Ichthyosis acquisita ,Prostate adenocarcinoma ,Pathology ,medicine.medical_specialty ,Keratosis ,business.industry ,medicine ,Dermatology ,medicine.symptom ,medicine.disease ,business ,Leser–Trélat sign - Published
- 2009
26. Do you know this syndrome?
- Author
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Renata Hubner Frainer, Giselle Martins Pinto, Luana Pizarro Meneghello, Luciana Boff de Abreu, and André Vicente Esteves de Carvalho
- Subjects
medicine.medical_specialty ,Adolescent ,genetic structures ,vision disorders ,Dermatology ,Hypotrichosis ,Congenital abnormalities ,Pathogenesis ,Macular Degeneration ,medicine ,Humans ,Congenital hypotrichosis ,medicine.diagnostic_test ,Cadherin ,business.industry ,Syndrome ,Macular dystrophy ,Macular degeneration ,medicine.disease ,eye diseases ,Hair loss ,Vision disorders ,Eye examination ,Etiology ,Syndrome In Question ,Female ,sense organs ,business - Abstract
Congenital hypotrichosis and Stargardt macular dystrophy are rare autosomal recessive disorder of unk nown etiology respectively characterized by hair loss, macular degeneration and severe progressive vision reduc tion. There are few reports in the literature with this association. Studies show that the defective gene is on the chro mosome I6q22.1 and involve cadherin molecule in the pathogenesis. Early recognition of these disorders often starts with hair changes and should alert the dermatologist for an eye examination thereby avoiding more severe ocular defect.
- Published
- 2013
27. Acknowledgement to Referees for Skin Appendage Disorders 2016
- Author
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Luiza Alonso Pereira, Adam S. Aldahan, Michelangelo La Placa, Bianca Maria Piraccini, Giulia Rech, Amanda Artis, Efstathios Rallis, Evangelia Bozi, Konstantina Diamanti, Damia L. Vendramini, Leandro Noriega, Chariklia Spiliadi, Antigoni Alevizou, Marius Florin Coros, Emilie Tournier, Adam I. Rubin, Vincent M. Hsu, Lucy L. Chen, Claudia Cavallotti, Jerry Shapiro, Jon Holmes, George Aravanis, Vincent Sibaud, Jean-Pierre Delord, Ana Letícia Boff, Leandro Damiani, Mariya I. Miteva, Şirin Yaşar, Raymond M. Fertig, Mengensatzproduktion, Gabriella Fabbrocini, Riccardo Balestri, Pierre Halteh, Wilma Bergfeld, Tudor Pinteala, Stephanie Mlacker, Keyvan Nouri, Miruna Negulescu, Paraskevi-Aikaterini Pierrakou, Jhessica Andrade, Maíra Rochael, Marcelo Teixeira, Vidhi V. Shah, Nilton Gioia Di Chiacchio, Pembegül Güneş, Druckerei Stückle, Shari Lipner, Mariana Vale Scribel da Silva, Claudio Marasca, Sema Aytekin, Dimitrios Sgouros, Nilton Di Chiacchio, Simona Stolnicu, Emre Kaynak, Fatih Göktay, Adina Coroaba, Maria Fernanda Reis Gavazzoni-Dias, Alexandros C. Katoulis, Ramon Grimalt, Anca Chiriac, Slimane Zerdoud, Dimitra Daskari, Aikaterini I. Liakou, Anca Eduard Chiriac, Irina Rosca, Cynthia Magro, Antonella Tosti, Dimitra Lianou, Jessica S. Haber, Shari R. Lipner, Serge Boulinguez, Rodrigo Pirmez, Giselle Martins Pinto, Letícia Arsie Contin, Celso Tavares Sodré, Cristian Podoleanu, Manasmon Chairatchaneeboon, Francesca Larese Filon, Richard Scher, Maria Mariano, Elisa Raquel Martins da Costa Marques, Matteo Megna, Raymond Fertig, Robert Baran, Richard K. Scher, Luca Muscardin, Carlo Renè Girardelli, Dimitrios Rigopoulos, Norma Cameli, Giuseppe Monfrecola, Vasileia Damaskou, Dimitris Rigopoulos, Bruno R.L. Silveira, Fernanda Musa Aguiar, Zafer Küçükodacı, Ioannis Panayiotides, Flávia Cury Rezende, Bruna Duque-Estrada, and Mariana Pinteala
- Subjects
medicine.medical_specialty ,business.industry ,Acknowledgement ,Medicine ,Dermatology ,Anatomy ,business ,Skin appendage - Published
- 2016
28. Classical Ehlers-Danlos syndrome: clinical, Histological and ultrastructural aspects
- Author
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Giselle Martins Pinto, Luis Antônio Suita de Castro, Fabiano Bonow de Almeida, Hiram Larangeira de Almeida, and Eduardo de Barros Coelho Bicca
- Subjects
Male ,Pathology ,medicine.medical_specialty ,Materials science ,Scars ,Dermatology ,Anatomy ,medicine.disease ,medicine.anatomical_structure ,Dermis ,Microscopy, Electron, Transmission ,Ehlers–Danlos syndrome ,Transmission electron microscopy ,Microscopy ,medicine ,Ultrastructure ,Humans ,Ehlers-Danlos Syndrome ,Fiber ,Collagen ,medicine.symptom ,Wound healing ,Child ,Skin - Abstract
A 12-year-old boy with difficulty in wound healing and scars of unusual appearance was examined. Thin, shiny and protruding skin, characterizing pseudotumoral lesions, was observed on his knees and elbows. Loose joints and increased skin elasticity were also observed. Light microscopy showed rare collagen bundles and loosely dispersed collagen fibers. Irregularly distributed elastic tissue was observed, and transmission electron microscopy revealed disorganized collagen fibers. In cross sections under high magnifications, fibers of varying diameters could be seen, as well as an irregular fiber outline. Scanning electron microscopy of the dermis showed disorganized collagen fibers, which were rarely arranged in bundles. Isolated and crossed-over fibers were also found
- Published
- 2010
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