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Case Report

A Rare Report of Vaginal Rhabdomyosarcoma

Ananya Das, Subrat Panda, Anusuya Sarma, Biswajit Dey

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Indian Journal of Obstetrics and Gynecology 10(4):p 199-202, October-December 2022. | DOI: https://doi.org/10.21088/ijog.2321.1636.10422.3

How Cite This Article:

Ananya Das, Subrat Panda, Anusuya Sarma, et. al./A Rare Report of Vaginal Rhabdomyosarcoma/Indian J Obstet Gynecol. 2022;10(4):199–202.

Timeline

Received : March 10, 2022         Accepted : April 12, 2022          Published : December 25, 2022

Abstract

Sarcomas are connective tissue cancers and Rhabdomyosarcomas are cancers originating from the skeletal muscle cells of the body. A 23 year old female unmarried, nulligravida presented in our emergency with the complaint of bleeding per vagina on and off since last 4 months. The lesion measured 9.2 (cc) x8.7 (cs)x7.8 (ap) cm. The lesion displaced the uterus superiorly distended the vaginal canal compressed the urinary bladder and urethra anteriorly but with no evidence of infiltration into the pelvic side wall and with maintained fat plane. Rest all pelvic organs as well as abdominal organs were within normal limit. The HPE report on microscopic examination of the tissue showed features suggestive of malignant spindle cell neoplasm. Immunohistochemistry was done and IHC report showed: Positive for Desmin, Myogenin predominantly cytoplasmic positive. Correlating the morphologic and IHC markers the report came to be Embryonal Rhabdomyosarcoma (Botryoid Rhabdomyosarcoma). As soon as the final diagnosis was made patient was referred to Department of Oncology and chemotherapy with Cyclophosphamide was started. She has been on regular follow up since then and is keeping well. The presence of a cervical polyp in an adolescent is a gynecologic oddity and must necessarily be examined histologically because it might be a rhabdomyosarcoma. This is extremely important because diagnosis at an early stage of the disease is a highly favorable prognostic factor.


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Data Sharing Statement

There are no additional data available. All raw data and code are available upon request.

Funding

This research received no funding.

Author Contributions

All authors contributed significantly to the work and approve its publication.

Ethics Declaration

This article does not involve any human or animal subjects, and therefore does not require ethics approval.

Acknowledgements

We would like to express our gratitude to the patients, their families, and all those who have contributed to this study.

Conflicts of Interest

No conflicts of interest in this work.


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Cite this article

Ananya Das, Subrat Panda, Anusuya Sarma, et. al./A Rare Report of Vaginal Rhabdomyosarcoma/Indian J Obstet Gynecol. 2022;10(4):199–202.


Licence:

Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.


Received Accepted Published
March 10, 2022 April 12, 2022 December 25, 2022

DOI: https://doi.org/10.21088/ijog.2321.1636.10422.3

Keywords

Vaginal RhabdomyosarcomaBleeding per vaginaMesenchymal cells

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Received March 10, 2022
Accepted April 12, 2022
Published December 25, 2022

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Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.


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