Case for diagnosis. Stewart-Treves syndrome after mastectomy

Autor: Sato, Roberta Akeme de Oliveira, Pinto, Clovis Antônio Lopes, Alves, Celia Antonia Xavier de Moraes, Ferreira, Juliana Arêas de Souza Lima Beltrame

Publikováno v: In Anais Brasileiros de Dermatologia September-October 2022 97(5):651-653

Panniculitis associated with amyopathic dermatomyositis

Autor: Azevedo, Paula de Oliveira, Castellen, Natalia Roberta, Salai, Ana Flávia, Barbosa, Fernanda Santana, Alves, Célia Antônia Xavier de Moraes, Pinto, Clóvis Antonio Lopes

Publikováno v: Anais Brasileiros de Dermatologia v.93 n.1 2018
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD
Anais Brasileiros de Dermatologia, Volume: 93, Issue: 1, Pages: 119-121, Published: FEB 2018

Panniculitis is a rare clinical finding in dermatomyositis, with less than 30 cases reported and there is only one case associated with the amyopathic subtype described in the literature. The present report describes a 49-year-old female patient that

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0910238c7c92b8334f38a544c3418ae4
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962018000100119

Scleromyxedema: clinical diagnosis and autopsy findings

Autor: Sala,Ana Carolina Bulhões, Cunha,Paulo Rowilson, Pinto,Clóvis Antônio Lopes, Alves,Célia Antônia Xavier de Moraes, Paiva,Ingrid Barreto, Araujo,Ana Paula Vieira

Publikováno v: Anais Brasileiros de Dermatologia, Volume: 91, Issue: 5 Supplement 1, Pages: 48-50, Published: OCT 2016
Anais Brasileiros de Dermatologia v.91 n.5 suppl.1 2016
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD

Scleromyxedema is a rare chronic cutaneous mucinosis of unknown etiology. It is characterized by papular eruption and scleroderma with microscopic evidence of mucin deposition, fibroblast proliferation, and fibrosis. Most patients with scleromyxedema

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f40b2b35cf454aca7c3cd25db04785ec
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100048&lng=en&tlng=en

Bannayan-Riley-Ruvalcaba syndrome with deforming lipomatous hamartomas in infant - Case report

Autor: Gontijo, Gabriela Maria Abreu, Pinto, Clóvis Antonio Lopes, Rogatto, Silvia Regina, Cunha, Isabela Werneck da, Aguiar Junior, Samuel, Alves, Célia Antônia Xavier de Moraes

Publikováno v: Anais Brasileiros de Dermatologia, Volume: 88, Issue: 6, Pages: 982-985, Published: DEC 2013

Bannayan-Riley-Ruvalcaba Syndrome is a rare condition caused by mutations in the PTEN gene. It displays association of multiple lipomas, macrocephaly, hemangiomas, hamartomatous intestinal polyposis, developmental delay and speckled pigmented maculae

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______608::16a86c80567d90bb72032a5134ac5e82
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000600982&lng=en&tlng=en

Panniculitis associated with amyopathic dermatomyositis.

Autor: Azevedo PO; (Dermatology Service, Faculdade de Medicina de Jundiaí (FMJ) - Jundiaí (SP), Brasil., Castellen NR; (Dermatology Service, Faculdade de Medicina de Jundiaí (FMJ) - Jundiaí (SP), Brasil., Salai AF; (Dermatology Service, Faculdade de Medicina de Jundiaí (FMJ) - Jundiaí (SP), Brasil., Barbosa FS; (Dermatology Service, Faculdade de Medicina de Jundiaí (FMJ) - Jundiaí (SP), Brasil., Alves CAXM; (Dermatology Service, Faculdade de Medicina de Jundiaí (FMJ) - Jundiaí (SP), Brasil., Pinto CAL; Department of Pathology, Faculdade de Medicina de Jundiaí (FMJ) - Jundiaí (SP), Brasil.; Pathology Service, Hospital AC Camargo - São Paulo (SP), Brasil.

Publikováno v: Anais brasileiros de dermatologia [An Bras Dermatol] 2018 Jan-Feb; Vol. 93 (1), pp. 119-121.