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A case of Cowden's syndrome associated with Lhermitte-Duclos disease / 대한내과학회지
Korean Journal of Medicine ; : S31-S34, 2009.
Artículo en Coreano | WPRIM | ID: wpr-105035
ABSTRACT
Cowden's disease, or multiple hamartoma syndrome, is an uncommon autosomal dominant condition characterized by mucocutaneous lesions and systemic malignancies. Lhermitte-Duclos disease, or dysplastic gangliocytoma of the cerebellum, is a rare cerebellar lesion that can cause mass effects in the posterior fossa. It may occur sporadically, or in association with Cowden's syndrome. We report a case of Cowden's disease associated with Lhermitte-Duclos disease in a 49-year-old man who underwent a routine checkup
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Síndrome de Hamartoma Múltiple Límite: Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2009 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Síndrome de Hamartoma Múltiple Límite: Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2009 Tipo del documento: Artículo