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Congenital multiple clustered dermatofibroma and multiple eruptive dermatofibromas--unusual presentations of a common entity
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Orientador(es)
Resumo(s)
Dermatofibroma is one of the most common entities seen in dermatology clinical practice. Several clinical subtypes have nevertheless been described, all of them of uncommon occurrence. The authors present two rare clinical variants of dermatofibromas: congenital multiple clustered dermatofibroma (the presented case is the 4th congenital case to be reported so far) and multiple eruptive dermatofibromas developing in the setting of a Sjögren's syndrome. Since the uncommon subtypes may not be clinically evident, dermatologists should familiarize themselves with their main features and we advise a high level of clinical suspicion in order to reach the correct diagnosis.
Descrição
Palavras-chave
Adult children Congenital abnormalities Histiocytoma benign fibrous Sjogren's Syndrome
Contexto Educativo
Citação
Pinto-Almeida, Teresa, Caetano, Mónica, Alves, Rosário, & Selores, Manuela. (2013). Congenital multiple clustered dermatofibroma and multiple eruptive dermatofibromas - unusual presentations of a common entity. Anais Brasileiros de Dermatologia, 88(6, Suppl. 1), 63-66. Retrieved July 31, 2014, from http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000800063&lng=en&tlng=en. 10.1590/abd1806-4841.20132647
Editora
Sociedade Brasileira de Dermatologia