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[Mixed germ cell tumor of the ovary with rhabdomyosarcomatous component. A case report].

Authors :
Bel Haj Salah M
Brahim EB
Zidi YS
Tangour M
Kilani H
Chatti-Dey S
Source :
Annales de pathologie [Ann Pathol] 2010 Oct; Vol. 30 (5), pp. 394-7. Date of Electronic Publication: 2010 Oct 16.
Publication Year :
2010

Abstract

Malignant germ cell tumors of the ovary are rare representing 3% of all ovarian neoplasms. Hence, they are the most common ovarian malignancy in girls and young women and account for approximately two-thirds of the ovarian cancers that occur in the first two decades of life. Germ cell tumors constitute a heterogeneous group of tumors and are often mixed associating at least two different tumoral components. Exceptionally, sarcomatous areas can be found. We present a case of a 15-year old girl admitted for a voluminous left ovarian mass revealed by pelvic pain. Pathological examination of the dissected material revealed the tumor to be a mixed germ cell tumor (immature teratoma and yolk sac tumor) with rhabdomyosarcomatous component of embryonal type. Clinico-pathological characteristics of such ovarian tumors will be discussed with emphasis on diagnostic difficulties.<br /> (Copyright © 2010 Elsevier Masson SAS. All rights reserved.)

Details

Language :
French
ISSN :
0242-6498
Volume :
30
Issue :
5
Database :
MEDLINE
Journal :
Annales de pathologie
Publication Type :
Academic Journal
Accession number :
21055529
Full Text :
https://doi.org/10.1016/j.annpat.2010.06.002