A
dysgerminoma is a type of
germ cell tumor; it usually is
malignant and usually occurs in the
ovary.
A tumor of the identical
histology but not occurring in the ovary may be described by an alternate name:
seminoma in the
testis or
germinoma in the
central nervous system or other parts of the body.
Dysgerminoma is the most common type of
malignant germ cell ovarian cancer, although it accounts for less than 1% of ovarian tumors overall. Dysgerminoma usually occurs in
adolescence and early adult life; about 5% occur in pre-pubertal children. Dysgerminoma is extremely rare after age 50. Dysgerminoma occurs in both ovaries in 10% of patients and, in a further 10%, there is microscopic tumor in the other ovary.
Abnormal
gonads (due to
gonadal dysgenesis and
androgen insensitivity syndrome) have a high risk of developing a dysgerminoma. Most dysgerminomas are associated with elevated serum
lactic dehydrogenase (LDH), which is sometimes used as a
tumor marker.
Presentation
They are exceptionally associated with hypercalcemia. On gross examination, dysgerminomas present with a smooth,
bosselated (knobby) external surface, and is soft, fleshy and either cream-coloured, gray, pink or tan when cut. Microscopic examination typically reveals uniform cells that resemble primordial germ...
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