Intestinal tumors in neurofibromatosis 1 with special reference to fatal gastrointestinal stromal tumors (GIST)
Author:
Affiliation:
1. Department of Cell Biology and Anatomy University of Turku Turku Finland
2. Department of Pulmonary Diseases Turku University Hospital Turku Finland
3. Department of Dermatology Turku University Hospital Turku Finland
Funder
Syöpäjärjestöt
Turun Yliopistollinen Keskussairaala
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.927
Reference29 articles.
1. Gastrointestinal manifestations of neurofibromatosis type 1 (Recklinghausen's disease): Clinicopathological spectrum with pathogenetic considerations;Agaimy A.;International Journal of Clinical and Experimental Pathology,2012
2. The importance of interstitial cells of cajal in the gastrointestinal tract
3. NF1-Associated Gastrointestinal Stromal Tumors Have Unique Clinical, Phenotypic, and Genotypic Characteristics
4. Gastrointestinal stromal tumours: ESMO–EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up
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1. Neurofibromatosis type I identified in a patient with four concurrent neoplasms (neurofibroma, GIST, pheochromocytoma and ampullary NET): a case report with literature review;2023-05-22
2. Neurofibromatosis type 1 with multiple gastrointestinal stromal tumors: A case report;World Journal of Clinical Cases;2023-04-06
3. Unusual presentation of GIST associated with type 1 neurofibromatosis: A case report;International Journal of Surgery Case Reports;2023-04
4. Challenges in the management of metastatic gastrointestinal stromal tumor in a patient with neurofibromatosis type 1: a case report;Journal of Medical Case Reports;2022-05-01
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