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Isolated ileal ganglioneuromatosis in an 11‑year‑old boy: Case report and review of literature.
Indian J Pathol Microbiol ; 2016 July-Sept 59(3): 365-367
Artículo en Inglés | IMSEAR | ID: sea-179581
ABSTRACT
Ganglioneuromatous proliferation in the gastrointestinal tract is a rare occurrence and is usually associated with specific syndrome complexes such as multiple endocrine neoplasia Type 2B or von Recklinghausen’s disease. We report here a case of diffuse intestinal ganglioneuromatosis, presenting as intestinal obstruction and chronic constipation in an 11‑year‑old boy. Sporadic cases of intestinal ganglioneuromatosis in the absence of any systemic manifestations are a very rare cause of enteric motility disorders in childhood, and we discuss the pathological and clinical significance of this finding. Histopathological identification of this uncommon cause of a common pediatric problem is important since the condition is amenable to surgical treatment.

Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Tipo de estudio: Estudio pronóstico Idioma: Inglés Revista: Indian J Pathol Microbiol Año: 2016 Tipo del documento: Artículo

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Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Tipo de estudio: Estudio pronóstico Idioma: Inglés Revista: Indian J Pathol Microbiol Año: 2016 Tipo del documento: Artículo