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Peripheral primitive neuroectodermal tumor (PNET) of the vulva: a case report

  • S. Halil1,*,
  • M. Kucuk2
  • M. Arvas3
  • Ö. Aydın4
  • Z.Z. Calay5

1Department of Obstetrics and Gynecology, Turkish Kidney Foundation, Hizmet Hospital, Istanbul

2Department of Obstetrics and Gynecology, Cine State Hospital, Cine, Aydin

3Department of Obstetrics and Gynecology, Istanbul University, Cerrahpasa School of Medicine, Istanbul

4Department of Pathology, Istanbul University, Cerrahpasa School of Medicine, Istanbul

5Department of Pathology, Eta Patoloji Akkavak Sok. Dilek, Nişantaşı, Istanbul, Turkey

DOI: 10.12892/ejgo201101117 Vol.32,Issue 1,January 2011 pp.117-118

Published: 10 January 2011

*Corresponding Author(s): S. Halil E-mail: saithalil@hotmail.com

Abstract

Introduction: Ewing's sarcoma/peripheral primitive neuroectodermal tumor (ES-PNET) is a high-grade malignant neoplasm that often develops in the skeletal system. Primary extraskeletal ES-PNET is an uncommon condition that rarely affects the female genital tract. Tumors in the ovary, cervix, and uterine corpus and vulva are occasionally reported. Reports on the Ewing family of tumors involving the vulva are extremely rare in the relevant literature. Only a few cases of vulvar ES-PNET have so far been reported. Case presentation: A 14-year-old adolescent girl presented to the clinic with a 4-month history of a left vulvar mass. The mass was excised under general anesthesia, and re-resection was performed three weeks later to obtain negative microscopic margins. The patient received chemotherapy and radiotherapy; however, she died of pulmonary metastasis within nine months of the initial surgery. Conclusion: In summary, we describe a rare case of vulvar ES-PNET with distinct rosette-like structures in a 14-year-old adolescent girl with a very poor prognosis.

Keywords

PNET; Vulva

Cite and Share

S. Halil,M. Kucuk,M. Arvas,Ö. Aydın,Z.Z. Calay. Peripheral primitive neuroectodermal tumor (PNET) of the vulva: a case report. European Journal of Gynaecological Oncology. 2011. 32(1);117-118.

References

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