2C73.1ICD-11 MMS 2026-01
Dysgerminoma of ovary
Description
A malignant germ cell tumour arising from the ovary. Morphologically, it is identical to seminoma and consists of a monotonous population of germ cells with abundant pale cytoplasm and uniform nuclei. The stroma invariably contains chronic inflammatory cells, mostly T-lymphocytes. It responds to chemotherapy or radiotherapy and the prognosis relates to the tumour stage.
Coding note from above levels
Includes Malignant neoplasm of skin of female genital organs
For use of this category, reference should be made to the mortality coding rules and guidelines in the Reference Guide.
Index terms
- Dysgerminoma of ovary
- Malignant dysgerminomatous germ cell tumour of ovary
- dysgerminoma, unspecified site, female
Inclusions
- Malignant dysgerminomatous germ cell tumour of ovary
Exclusions from above levels
2E05.0– Malignant neoplasm metastasis in ovary- http://id.who.int/icd/entity/1965082709 – Malignant mesenchymal neoplasms
2E05– Malignant neoplasm metastasis in female reproductive system
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- http://id.who.int/icd/entity/879154182 – Neoplasms of central nervous system or related structures
- http://id.who.int/icd/entity/944754984 – Neoplasms of haematopoietic or lymphoid tissues
Sibling codes
2C73.0– Carcinomas of ovary2C73.2– Granulosa cell malignant tumour of ovary2C73.3– Malignant teratoma of ovary2C73.4– Serous cystadenoma, borderline malignancy of ovary2C73.5– Endodermal sinus tumour, unspecified site, female2C73.Y– Other specified malignant neoplasms of the ovary2C73.Z– Malignant neoplasms of ovary, unspecified
Foundation entity
Dysgerminoma of ovary – http://id.who.int/icd/entity/208782658