gist
Table of Contents
gastrointestinal stromal tumors (GIST)
see also:
Introduction
- a rare type of GIT tumour (some are benign, some are malignant) believed to originate in cells found between muscle layers of the gastro-intestinal tract, called Interstitial cells of Cajal (ICC) and generally grow outwards
- 50-60% arise in the stomach
- 30-40% arise in small intestines
Aetiology
- increasing age
- genetic risk factors
- Neurofibromatosis type 1
- Carney Triad
- a rare syndrome defined by the coexistence of three specific tumours and typically affecting young people
Clinical features
- usually asymptomatic
- may cause pain, bloating, fatigue, occult or overt GIT bleeding
Diagnosis
- may be picked up on gastroscopy or CT scan
- biopsy to confirm benign vs malignant status
Treatment
- most are treated with surgical excision
- imatinib is used to treat GIST that cannot be removed by surgery
gist.txt · Last modified: 2021/07/29 03:51 by gary1