 Dysgerminoma
"Dysgerminoma" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
| Descriptor ID |
D004407
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| MeSH Number(s) |
C04.557.465.330.300
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| Concept/Terms |
Dysgerminoma- Dysgerminoma
- Dysgerminomas
- Disgerminoma
- Disgerminomas
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Below are MeSH descriptors whose meaning is more general than "Dysgerminoma".
Below are MeSH descriptors whose meaning is more specific than "Dysgerminoma".
This graph shows the total number of publications written about "Dysgerminoma" by people in this website by year, and whether "Dysgerminoma" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 1 | 0 | 1 | | 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Dysgerminoma" by people in Profiles.
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Nasioudis D, Mastroyannis SA, Latif NA, Ko EM. Trends in the surgical management of malignant ovarian germcell tumors. Gynecol Oncol. 2020 04; 157(1):89-93.
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Kanakatti Shankar R, Inge TH, Gutmark-Little I, Backeljauw PF. Oophorectomy versus salpingo-oophorectomy in Turner syndrome patients with Y-chromosome material: clinical experience and current practice patterns assessment. J Pediatr Surg. 2014 Nov; 49(11):1585-8.
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Cost NG, Ludwig AT, Wilcox DT, Rakheja D, Steinberg SJ, Baker LA. A novel SOX9 mutation, 972delC, causes 46,XY sex-reversed campomelic dysplasia with nephrocalcinosis, urolithiasis, and dysgerminoma. J Pediatr Surg. 2009 Feb; 44(2):451-4.
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Crawford ED, Goodman P, Nabors WL, Stephens RL, Khan K, Pass LM, Smith AY, Christie DW. Treatment of stages B3 and C seminoma with chemotherapy followed by irradiation therapy. Southwest Oncology Group Study. Urology. 1992 May; 39(5):457-60.
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