Solitary Malignant Gastrointestinal Stromal Tumor Associated with a Neurofibromatosis Type I
Annals of Dermatology
;
: 12-14, 2003.
Artículo
en Inglés
| WPRIM
| ID: wpr-194044
ABSTRACT
From the Department of Dermatology, College of Medicine, The Catholic University of Korea, Kangnam St. Mary's Hospital, 505, Banpo-Dong, Seocho-Gu, 137-040, Seoul, Korea, Gastrointestinal stromal tumors are usually late manifestations of neurofibromatosis (von Recklinghausen's disease) and most become clinically apparent in middle-aged patients as multiple benign tumors. To our review of the literature, solitary malignant stromal tumor of gastrointestinal tract is exceptionally rare in von Recklinghausen's disease. We herein present a case of solitary jejunal stromal tumor in a 50-year-old woman with NF1, which histopathologically showed a malignant change and combined smooth muscle-neural type.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Neurofibromatosis 1
/
Neurofibromatosis
/
Tracto Gastrointestinal
/
Tumores del Estroma Gastrointestinal
/
Dermatología
/
Seúl
/
Corea (Geográfico)
Límite:
Femenino
/
Humanos
País/Región como asunto:
Asia
Idioma:
Inglés
Revista:
Annals of Dermatology
Año:
2003
Tipo del documento:
Artículo
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