Gastrointestinal Stromal Tumors of Neurofibromatosis Type I: A Case Report
Published: 2023-03-18
Page: 97-101
Issue: 2023 - Volume 6 [Issue 1]
Erguibi Driss
Ain Chock, Casablanca, Morocco.
El Maghraoui Omar *
Ain Chock, Casablanca, Morocco.
Essaidi Zakaria
Hajri Amal
Ain Chock, Casablanca, Morocco.
Boufettal Rachid
Ain Chock, Casablanca, Morocco.
Eljai Saad Rifki
Ain Chock, Casablanca, Morocco.
Chehab Farid
Ain Chock, Casablanca, Morocco.
*Author to whom correspondence should be addressed.
Abstract
Von Recklinghausen’s disease or neurofibromatosis type 1 is an autosomal dominant condition that affects the central nervous system.
A 52-year-old female with known Von Recklinghausen's disease (VRD) presented with abdominal pain. A physical examination found multiple cutaneous and subcutaneous nodules and Café-au-lait pigmentation all over the body. A CT scan of the abdomen showed heterogeneously abdominal mass.she underwent surgical resection. Pathological diagnosis and immunohistochemical was gastrointestinal stromal tumor.
GISTs represent the most common gastrointestinal manifestation of NF1, sporadic GISTs arise predominantly in the stomach, about 90% of Von Recklinghausen’s disease Patients have a tendency to develop GISTs wich located in the small intestine usually in the jejunum and characterized by their tendency for multiplicity.
Gastrointestinal stromal tumors associated Von Recklinghausen’s disease has been described to comprise a minority of cases, We report a clinical case of the association of GIST with NF1 in whom surgical resection was performed.
Keywords: Neurofibromatosis type I, GIST, tumors, gastrointestinal stromal tumors