Erschienen in:
01.09.2009 | Case Report
Extraskeletal neuroectodermal tumour of the vagina: a single case report and review
verfasst von:
Halima Al-tamimi, Alia A. Al-Hadi, Al-Hareth Al-Khater, Issam Al-bozom, Najla Al-sayed
Erschienen in:
Archives of Gynecology and Obstetrics
|
Ausgabe 3/2009
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Abstract
A case report and review of an extraskeletal neuroectodermal tumour of the vagina.
Background
Ewing’s sarcoma (ES) and primitive neuroectodermal tumours (PNETs) account for approximately 6–10% of primary malignant bone tumours and, following osteosarcoma, are the second most common group of bone sarcomas in children. Ewing’s sarcoma rarely affects the genitourinary tract.
Case summary
We report a rare case of extraskeletal Ewing’s sarcoma diagnosed in a 47-year-old Indian woman presenting with a simple cystic lesion in the posterior wall of the vagina. The histopathology revealed a rare presentation of a primitive malignant extraskeletal neuroectodermal tumour.
Conclusion
As our PubMed review found only six previously reported cases of vaginal extraskeletal Ewing’s sarcoma. Presentation as vaginal masses helped in early disease detection.