Familial dysgerminoma associated with 46, XX pure gonadal dysgenesis.

Bahia Namavar-Jahromi, Mitra Mohit, Perikala V Kumar
Author Information
  1. Bahia Namavar-Jahromi: Department of Obstetrics and Gynecology, Shiraz Univeristy of Medical Sciences, Iran. namavarb@sums.ac.ir

Abstract

Although the occurrence of pure gonadal dysgenesis PGD is usually sporadic and nonfamilial, here we present 3 sisters with 46, XX PGD, who are born from a first cousin marriage. Review of their family pedigree is compatible with autosomal recessive inheritance. Surprisingly, 2 of these sisters developed ovarian tumors. Both showed the pathological result of dysgerminoma with syncytiotrophoblastic giant cells. These 2 cases are examples of tumorigenesis in PGD without an identifiable Y chromosome. Therefore, malignant degeneration of the streak gonads should be considered in the patients with 46, XX PGD.

MeSH Term

Adult
Chromosome Disorders
Consanguinity
Dysgerminoma
Female
Genes, Recessive
Giant Cells
Gonadal Dysgenesis, 46,XX
Humans
Iran
Ovarian Neoplasms
Trophoblasts

Word Cloud

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