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