A case of generalized ostraceous psoriasis mimicking dermatitis neglecta

Autor: Bianca Angelina Macêdo do Nascimento, Alessandra Haber Carvalho, Carolina Moraes Dias, Thaiane Lima Lage, Clívia Maria Oliveira Carneiro, Maraya de Jesus Semblano Bittencourt

Publikováno v: Anais Brasileiros de Dermatologia, Vol 90, Iss 3 suppl 1, Pp 197-199 (2015)

AbstractLithium has been implicated in the exacerbation of pre-existing psoriasis, in the induction of psoriasis on previously uninvolved skin of psoriasis patients, and in the triggering of psoriasis for the first time in patients without a personal

Externí odkaz: https://doaj.org/article/55ea39e5ef724219bd1986429ca325d2

Case for diagnosis

Autor: Thaiane Lima Lage, Mario Fernando Ribeiro de Miranda, Maraya de Jesus Semblano Bittencourt, Carolina Moraes Dias, Amanda Magno de Parijós, Theisla Kely Azevedo Raiol

Publikováno v: Anais Brasileiros de Dermatologia, Vol 88, Iss 6, Pp 1005-1007 (2013)

Granular cell tumor is a rare benign neoplasm of neural origin. We report the case of a female patient, 27 years old presenting a brown-red nodule in the right arm, which pathological examination showed to be formed by polygonal cells with eosinophil

Externí odkaz: https://doaj.org/article/d9af6fc840ea457fbb85bb037e4e88a5

Langerhans cell histiocytosis with nail changes and multisystem disease: a case report

Autor: Carolina Moraes Dias, Alessandra Haber Carvalho, Letícia Brito Mesquita, Thaiane Lima Lage, Maraya de Jesus Semblano Bittencourt, Amanda Magno de Parijós

Publikováno v: de Jesus Semblano Bittencourt, Maraya; Moraes Dias, Carolina; Lima Lage, Thaiane; Magno Parijós, Amanda; Brito Mesquita, Letícia; & Haber Carvalho, Alessandra. (2016). Langerhans cell histiocytosis with nail changes and multisystem disease: a case report. Dermatology Online Journal, 22(7). Retrieved from: http://www.escholarship.org/uc/item/0n60013n

Nail involvement in Langerhans cell histiocytosis is uncommon and is said to indicate a poor prognosis. We describe a 2-year-old boy with onycholysis, subungual hyperkeratosis, and hemorrhages on his fingernails. He also had hepatosplenomegaly and pu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c2d1e82f5b40a4b7025f78bf3f4e7d7
http://www.escholarship.org/uc/item/0n60013n

Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis -- case report

Autor: Maraya de Jesus Semblano Bittencourt, Renata Silva Barros, Waldonio de Brito Vieira, Thaiane Lima Lage, Carolina Moraes Dias, Otavio Augusto Gomes Paz

Publikováno v: Anais Brasileiros de Dermatologia

Behçet's disease is a chronic inflammatory disease of unknown aetiology, characterized by recurrent oral and genital aphthous ulcerations, uveitis, skin lesions and other multisystem affections associated with vasculitis. Different types of vessels,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abdd092b1e95e3b7d3c00471bfa8f2d5
https://pubmed.ncbi.nlm.nih.gov/23793200