Dysgerminoma

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Retrieved
2021-01-18
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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 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.

Signs and symptoms

Excision of a dysgerminoma

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 cells. Typically, the stroma contains lymphocytes and about 20% of patients have sarcoid-like granulomas. Metastases are most often present in the lymph nodes.

Diagnosis

LDH tumour markers is elevated in 95% of the cases.

  • 1.jpg/300px-Dysgerminoma%2C_intermed._mag.1.jpg" decoding="async" width="300" height="200" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/b2/Dysgerminoma%2C_intermed._mag.1.jpg/450px-Dysgerminoma%2C_intermed._mag.1.jpg 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/b2/Dysgerminoma%2C_intermed._mag.1.jpg/600px-Dysgerminoma%2C_intermed._mag.1.jpg 2x" data-file-width="4272" data-file-height="2848">

    Dysgerminoma characterized by uniform cells separated by fibrous septa with lymphocytes, H&E stain.

  • Low-power view of a dysgerminoma infiltrating the colonic wall, H&E stain.

Treatment

Dysgerminomas, like other seminomatous germ cell tumors, are very sensitive to both chemotherapy and radiotherapy. For this reason, with treatment patients' chances of long-term survival, even cure, is excellent. Targeted treatments for dysgerminomas that do not respond to chemotherapy are being evaluated.