Literature DB >> 31175959

Gonadoblastoma-Associated Mixed Gonadal Germ Cell Tumor with Dysgerminoma and Hepatoid Yolk Sac Tumor Components in 46XY Gonadal Dysgenesis.

Daniele M Losada1, Cristina L Benetti-Pinto2, Liliana A L A Andrade3.   

Abstract

BACKGROUND: Disorders of sex development are congenital conditions with atypical chromosomal, gonadal, or anatomical sex development. Gonadal dysgenesis in patients containing a Y chromosome have a high risk of developing germ cell tumors with potential for malignant transformation. CASE: We present the case of a 17-year-old phenotypic female with primary amenorrhea and 46,XY complete gonadal dysgenesis. Pelvic ultrasound showed a solid cystic lesion in the right gonad. Pathology showed a gonadoblastoma-associated mixed gonadal germ cell tumor with dysgerminoma and hepatoid yolk sac tumor. SUMMARY AND
CONCLUSION: To our knowledge, this mixed neoplasm association has not been previously reported and this case illustrates the challenges for the diagnosis of gonadal dysgenesis-associated tumors, emphasizing its recognition and prognostic implications.
Copyright © 2019 North American Society for Pediatric and Adolescent Gynecology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  46,XY gonadal dysgenesis; Dysgerminoma; Gonadoblastoma; Primary amenorrhea; Yolk sac tumor; disorders of sex development

Mesh:

Year:  2019        PMID: 31175959     DOI: 10.1016/j.jpag.2019.05.014

Source DB:  PubMed          Journal:  J Pediatr Adolesc Gynecol        ISSN: 1083-3188            Impact factor:   1.814


  1 in total

1.  A rare case of ovarian gonadoblastoma flourishing into malignant mixed germ cell tumour with review of literature.

Authors:  Tarang Patel; Bhamini Jakhetiya; Ashish Jakhetiya; Virendrakumar Meena
Journal:  Int Cancer Conf J       Date:  2022-01-06
  1 in total

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