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Neurofibromatosis Type 1 Presenting as Bleeding Jejunal Gastrointestinal Stromal Tumour.

Authors :
Liang, Raymond Fueng-Hin
Chau, Cora Yuk-Ping
Lim, Wee Chian
Source :
Case Reports in Gastroenterology. 2024, Vol. 18 Issue 1, p299-305. 7p.
Publication Year :
2024

Abstract

Introduction: Gastrointestinal stromal tumours (GISTs) are an important, though uncommon, cause of obscure gastrointestinal bleeding and may rarely be associated with genodermatoses such as neurofibromatosis type 1 (NF1). NF1-related GISTs have unique phenotypic features compared with sporadic GISTs and may elude diagnosis due to their predilection for the small bowel. Case Presentation: We report a case of a 45-year-old Singaporean woman with café-au-lait macules and cutaneous neurofibromas who presented with occult obscure gastrointestinal bleeding and was eventually discovered to have a bleeding jejunal GIST. This finding, considered together with her cutaneous signs, eventually led to the diagnosis of NF1. Conclusion: Genodermatoses and their gastrointestinal complications are likely under-reported in adult Southeast Asian populations and deserve greater awareness from gastroenterologists practising in this region. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16620631
Volume :
18
Issue :
1
Database :
Academic Search Index
Journal :
Case Reports in Gastroenterology
Publication Type :
Academic Journal
Accession number :
178030257
Full Text :
https://doi.org/10.1159/000538688