46, XX disorder of sexual development associated with mixed germ cell tumor of the prostate: a rare case report
Changrong Wang, Jiangli Du, Xueping Xiang, Yuyong Wang, Jingjing Xiang, Qiaoping Xu

TL;DR
A rare case of a 40-year-old male with a genetic disorder and a prostate tumor is reported, offering new insights into its genetic and clinical features.
Contribution
This is the first reported case of a 46, XX disorder of sex development with a mixed prostate germ cell tumor.
Findings
Whole-genome sequencing revealed a high somatic mutational load in the tumor cells.
The patient's karyotype was confirmed as 46, XX (SRY +), with specific hormonal and physical characteristics.
The case provides new insights into the clinicopathological and genetic profile of this rare condition.
Abstract
Extragonadal germ cell tumors originating from the prostate are exceptionally rare. To the best of our knowledge, there have been no reported cases of mixed germ cell tumors in individuals with 46 XX disorder of sex development. In this study, we conducted a comprehensive analysis using whole genome sequencing to investigate the clinicopathological and molecular genetic characteristics of a submitted case, with the objective of elucidating its underlying pathogenesis. A 40-year-old male patient was diagnosed with a combination of 46, XX disorder of sex development and a primary prostate mixed germ cell tumor with yolk sac tumor and teratoma components. Whole-genome sequencing revealed that the tumor cells had a high somatic mutational load. Analysis of genomic structural variations and copy number variants confirmed the patient's karyotype as 46, XX (SRY +). Additionally, the patient…
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Taxonomy
TopicsTesticular diseases and treatments · Sexual Differentiation and Disorders · Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
