CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2011; 32(03): 171-173
DOI: 10.4103/0971-5851.92823
CASE REPORT

Paravaginal peripheral primitive neuroectodermal tumor: A rare tumor

Samrat Dutta
Department of Radiotherapy, Medical College, Kolkata, West Bengal, India
,
Chandan Dasgupta
Department of Radiotherapy, Medical College, Kolkata, West Bengal, India
,
Kakoli Choudhury
Department of Radiotherapy, Medical College, Kolkata, West Bengal, India
› Author Affiliations

Abstract

Peripheral primitive neuroectodermal tumor (PNET) of the female genital tract, particularly those in the vaginal and paravaginal region, are extremely rare. A 36-year-old woman presented with clinical features similar to that of a case of cervical fibroid. It was only after surgery that the histopathology suggested it to be a malignant round cell tumour and was CD99 positive. She underwent adjuvant chemotherapy with the Ifosfamide and Etoposide alternating with Vincristine, Doxorubicin, and Cyclophosphamide regime and radical radiotherapy. She is disease free at 12 months of follow-up. The importance of immunostaining and adequate histopathology report lies in the fact that the correct diagnosis thus achieved enabled us to manage a rare case of paravaginal PNET with a multimodality approach.



Publication History

Article published online:
06 August 2021

© 2011. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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