Gonadoblastoma overview: Difference between revisions
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==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
The [[prevalence]] of gonadoblastoma depends on the [[Chromosome|chromosomal]] content, presence or absence of [[mosaicism]], gonadal [[histology]], and age of the patient and varies between 15,000 to 30,000 per 100,000 individuals worldwide. The [[incidence]] of gonadoblastoma varies according to the presence or absence of [[Y chromosome|Y chromosomal]] content and age of the individual. Patients with [[Turner syndrome]] who have [[Y chromosome|Y chromosomal]] content either completely or partially may develop gonadoblastoma with an [[incidence]] as high as 43,000 per 100,000 individuals worldwide. The [[incidence]] of gonadoblastoma among [[phenotypical]] [[females]] with XY [[gonadal]] [[abnormalities]] have been observed to be 40,000 per 100,000 individuals worldwide. Gonadoblastoma may be found at any age, but commonly presents before the age of 15 years. Since, it usually affects individuals with [[gonadal dysgenesis]], there is no [[genotype]]-[[phenotype]] [[correlation]]. [[Phenotype|Phenotypically]], it tends to affect [[female]] individuals to a greater extent. | |||
==Risk Factors== | ==Risk Factors== | ||
Revision as of 19:39, 20 February 2019
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Gonadoblastoma Microchapters |
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Gonadoblastoma overview On the Web |
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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.
Causes
There are no established causes for gonadoblastoma. However, there are certain risk factors that predispose to increased risk of gonadoblastoma.
Differentiating Xyz from Other Diseases
Gonadoblastoma must be differentiated from other diseases that cause virilization, and primary amenorrhea and also must be differentiated pathologically from dysgerminoma, Sex-cord stromal tumors, and Sertoli-cell nodules.
Epidemiology and Demographics
The prevalence of gonadoblastoma depends on the chromosomal content, presence or absence of mosaicism, gonadal histology, and age of the patient and varies between 15,000 to 30,000 per 100,000 individuals worldwide. The incidence of gonadoblastoma varies according to the presence or absence of Y chromosomal content and age of the individual. Patients with Turner syndrome who have Y chromosomal content either completely or partially may develop gonadoblastoma with an incidence as high as 43,000 per 100,000 individuals worldwide. The incidence of gonadoblastoma among phenotypical females with XY gonadal abnormalities have been observed to be 40,000 per 100,000 individuals worldwide. Gonadoblastoma may be found at any age, but commonly presents before the age of 15 years. Since, it usually affects individuals with gonadal dysgenesis, there is no genotype-phenotype correlation. Phenotypically, it tends to affect female individuals to a greater extent.