2B5D.0ICD-11 MMS 2026-01
Malignant mixed epithelial mesenchymal tumour of ovary
Description
Malignant mixed epithelial mesenchymal tumour of the ovary is a rare and very aggressive neoplasm presenting most commonly in postmenopausal women and is composed of adenocarcinomatous and sarcomatous elements and, depending on the types of these elements, can be classified as homologous or heterologous. It often has a poor prognosis.
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
- Malignant mixed epithelial mesenchymal tumour of ovary
- Malignant mixed epithelial mesenchymal tumour of the ovary
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
Malignant mixed epithelial mesenchymal tumour of ovary – http://id.who.int/icd/entity/2072916704
Allowed postcoordination axes
Part of: 2B5D: Malignant mixed epithelial mesenchymal tumour, primary site › 02: Neoplasms