Section Editor: Dharam M. Ramnani, MD

Virginia Urology, Richmond, VA, USA

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Genetics of Gonadoblastoma: Gonadoblastoma develops in patients with gonadal dysgenesis which is a disorder of sex development. It is caused by mutations or deletions in one or more genes required for the development of physiological male phenotype. The gonadal tissue must contain Y chromosome (or portion of Y chromosome containing TSPY locus). The involved genes include WT1, SOX9, SF1, and SRY among others.

Treatment and Prognosis: Gonadoblastoma is considered to be a premalignant lesion which can give rise to germ cell tumors, usually seminomas, but any non-seminomatous germ cell tumor can develop. The risk of malignancy can be estimated by observing the degree of external masculinization. The risk is highest in individuals with ambiguous phenotype; intermediate in boys with mild undervirilization; and lowest among girls with Turner syndrome phenotype.

Gonadectomy before the development of a germ cell tumor is curative. The gonadal excision is done bilaterally because of association of gonadoblastoma with gonadal dysgenesis and high frequency of bilaterality of this tumor (almost 40% of cases).

The image shows germ cell neoplasia-in-situ like cells and sex cord-stromal cells (small dark hyperchromatic cells) arranged around basement membrane material (Call-Exner pattern).

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