Abstract
Neurofibromatosis type 1 (NF1) is a genetic disorder commonly associated with cutaneous, neurologic, and orthopedic manifestations. It is the most frequent of the so-called hamartoses. This syndrome results from a mutation in or deletion of the NF1 gene. The gene product neurofibromin serves as a tumor suppressor, and decreased production of this protein results in a myriad of clinical features. GI stromal tumors, often multiple, with a predilection for the small bowel, may be seen in patients with NF1. 1 Hochberg F.H. Dasilva A.B. Gadalbini J. Gastrointestinal involvement in von Recklinghausen's neurofibromatosis. Neurology. 1974; 24: 1144-1155 Crossref PubMed Google Scholar We report an unusual case of gastric plexiform neurofibroma of a patient who presented with upper-GI bleeding and partial intestinal obstruction.
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