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A Case of Cowden Disease Associated with Lhermitte-Duclos Disease / 대한소화기내시경학회지
Article em Ko | WPRIM | ID: wpr-185705
Biblioteca responsável: WPRO
ABSTRACT
Cowden disease (CD), also known as 'multiple hamartoma syndrome', is a rare autosomal dominant disorder with a high risk of breast, thyroid, or genitourinary malignancies. Lhermitte-Duclos Disease (LDD) is believed to be a hamartomatous overgrowth of cerebellar ganglion cells and currently is considered to be a part of CD. However, the report of the association between LDD and CD has been very unusual. We have recently experienced a 53-year-old man with LDD who had acral keratosis of extremities, gastrointestinal polyposis, and multinodular goiter. To our knowledge, it is the second case of CD associated with LDD in Korea. We report it with a review of the literatures.
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Texto completo: 1 Índice: WPRIM Assunto principal: Glândula Tireoide / Síndrome do Hamartoma Múltiplo / Mama / Cistos Glanglionares / Extremidades / Bócio / Hamartoma / Ceratose / Coreia (Geográfico) Limite: Humans País/Região como assunto: Asia Idioma: Ko Revista: Korean Journal of Gastrointestinal Endoscopy Ano de publicação: 2004 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Glândula Tireoide / Síndrome do Hamartoma Múltiplo / Mama / Cistos Glanglionares / Extremidades / Bócio / Hamartoma / Ceratose / Coreia (Geográfico) Limite: Humans País/Região como assunto: Asia Idioma: Ko Revista: Korean Journal of Gastrointestinal Endoscopy Ano de publicação: 2004 Tipo de documento: Article