Multiple gastrointestinal stromal tumors in type I neurofibromatosis: a pathologic and molecular study
- 1 April 2005
- journal article
- case report
- Published by Elsevier in Laboratory Investigation
- Vol. 18 (4) , 475-484
- https://doi.org/10.1038/modpathol.3800334
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Gastrointestinal Stromal Tumors and Other Mesenchymal Lesions of the GutLaboratory Investigation, 2003
- Polyclonal nature of diffuse proliferation of interstitial cells of Cajal in patients with familial and multiple gastrointestinal stromal tumoursGut, 2002
- Prognostic Value ofKITMutation Type, Mitotic Activity, and Histologic Subtype in Gastrointestinal Stromal TumorsJournal of Clinical Oncology, 2002
- Gain-of-function mutation at the extracellular domain of KIT in gastrointestinal stromal tumoursThe Journal of Pathology, 2001
- Gastrointestinal stromal tumor of the rectum with activating mutation of c- kitDiseases of the Colon & Rectum, 2000
- KIT Extracellular and Kinase Domain Mutations in Gastrointestinal Stromal TumorsThe American Journal of Pathology, 2000
- Gain-of-Function Mutations of c- kit in Human Gastrointestinal Stromal TumorsScience, 1998
- Multiple small intestinal stromal tumors with skeinoid fibers in association with neurofibromatosis 1 (von Recklinghausen's disease)Pathology International, 1996
- A Case of von Recklinghausen's Disease with Bilateral Pheochromocytoma-Malignant Peripheral Nerve Sheath Tumors of the Adrenal and Gastrointestinal Autonomic Nerve TumorsThe American Journal of Surgical Pathology, 1996
- Von Recklinghausen NeurofibromatosisNew England Journal of Medicine, 1981