2B5B.1ICD-11 MMS 2026-01
Gastrointestinal stromal tumour of small intestine
Description
A gastrointestinal stromal tumour that arises from the small intestine. It usually affects adults over fifty years of age. The majority of cases have spindle cell morphology. The prognosis depends on the tumour size and the mitotic activity.
Coding note from above levels
For use of this category, reference should be made to the mortality coding rules and guidelines in the Reference Guide.
Index terms
- Gastrointestinal stromal tumour of small intestine
- Malignant GIST - [gastrointestinal stromal tumour] of small intestine
- Gastrointestinal stromal tumour of jejunum
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- Gastrointestinal stromal tumour of ileum
- Gastrointestinal stromal tumour of Meckel diverticulum
- Gastrointestinal stromal tumour involving overlapping sites of small intestine
- Gastrointestinal stromal tumour of duodenum
- Malignant GIST - [gastrointestinal stromal tumour] of the duodenum
Exclusions from above levels
2A01.1– Mesenchymal tumour of meninges2A02.1– Tumours of cranial or paraspinal nerves- http://id.who.int/icd/entity/879154182 – Neoplasms of central nervous system or related structures
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- http://id.who.int/icd/entity/944754984 – Neoplasms of haematopoietic or lymphoid tissues
Sibling codes
Foundation entity
Gastrointestinal stromal tumour of small intestine – http://id.who.int/icd/entity/319870485
Allowed postcoordination axes
Part of: 2B5B: Gastrointestinal stromal tumour, primary site › 02: Neoplasms