Gonadoblastoma overview: Difference between revisions
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==Pathophysiology== | ==Pathophysiology== | ||
The exact [[pathogenesis]] of gonadoblastoma is not fully understood. [[Gonadal]] development starts at 5 weeks of [[gestation]] and continues according to [[sex chromosomes]]. Any [[defects]] in this complicated process leads to defective [[gonadal]] development and [[gonadal dysgenesis]] and subsequently, it may be converted to gonadoblastoma in 20% to 30% of the cases. | |||
==Causes== | ==Causes== |
Revision as of 18:50, 20 February 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]
Overview
Historical Perspective
Gonadoblastoma was first discovered by Dr. Scully in 1953. The association between GBY gene (GonadoBlastoma on the Y chromosome) and gonadoblastoma was made in 1986. In 1995, Tsuchiya found that the GBY gene located near the centromere of Y chromosome and contains multiple genes including Testis-specific protein Y-encoded (TSPY) gene.
Classification
Gonadoblastoma may be classified according to pathological appearance into three sub-types including classical, dissecting, and burnt-out.
Pathophysiology
The exact pathogenesis of gonadoblastoma is not fully understood. Gonadal development starts at 5 weeks of gestation and continues according to sex chromosomes. Any defects in this complicated process leads to defective gonadal development and gonadal dysgenesis and subsequently, it may be converted to gonadoblastoma in 20% to 30% of the cases.