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A Case of Reed's Syndrome(Familial Leiomyomatosis Cutis Et Uteri) / 대한피부과학회지
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-183509
Biblioteca responsável: WPRO
ABSTRACT
Reed's syndrome is a rare, autosomal dominant disease with incomplete penetrance that is characterized by uterine and cutaneous leiomyomas. We report a case of Reed's syndrome in a 50-year-old woman. The patient underwent removal of the uterine leiomyoma at the age of 36. Following this the patient noticed development of multiple, cutaneous nodules on both arms at the age of 45. These nodules progressively increased in both number and size, while appearing in other sites. The histopathologic finding of an isolated, single skin lesion showed typical leiomyoma arising from arrector pilorum muscle. Familial history revealed that her father had been affected with similar cutaneous lesions.
Assuntos

Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Braço / Pele / Leiomiomatose / Penetrância / Pai / Leiomioma Limite: Feminino / Humanos Idioma: Coreano Revista: Korean Journal of Dermatology Ano de publicação: 2007 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Braço / Pele / Leiomiomatose / Penetrância / Pai / Leiomioma Limite: Feminino / Humanos Idioma: Coreano Revista: Korean Journal of Dermatology Ano de publicação: 2007 Tipo de documento: Artigo
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