Structured Summary
Abstract
A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646)
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Classification
Broader headings
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Synonyms
3 entry terms
- Disgerminoma
- Disgerminomas
- Dysgerminomas
MeSH Record
Aspects Covered
39 allowable subheadings
Indexed with the subheadings blood, blood supply, cerebrospinal fluid, chemically induced, chemistry, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, secondary, surgery, therapy, ultrastructure, urine, veterinary, virology.
MeSH Record
Indexing Annotation
coordinate with probably OVARIAN NEOPLASMS
MeSH Record
History Note
79; was DISGERMINOMA 1963-78
MeSH Hierarchy
Tree Number
MeSH Record
NLM Classification
WP 322
AMA Style
References
- National Library of Medicine. Dysgerminoma. Medical Subject Headings (MeSH). 2026. Unique ID D004407. http://id.nlm.nih.gov/mesh/2026/D004407
- Dysgerminoma. In: Wikipedia. https://en.wikipedia.org/wiki/Dysgerminoma
- Dysgerminoma. In: Wikidata. https://www.wikidata.org/wiki/Q1269251