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Primary histiocytic sarcoma of the uterine cervix: an extremely rare entity Cover

Primary histiocytic sarcoma of the uterine cervix: an extremely rare entity

Open Access
|Mar 2017

Abstract

Objective. Histiocytic sarcoma (HS) is an extraordinary rare tumor and it has an offensive clinical course. HS of the uterine cervix is a far uncommon tumor with just a few cases described so far. Here we presented a case of primary HS of the uterine cervix in a 62-year-old female initially misdiagnosed as large cell non-keratinizing squamous cell carcinoma. To the best of our knowledge, this is the first reported case of HS of the uterine cervix from Iran.

Case report. The patient presented with post-menopausal vaginal bleeding. Further evaluations revealed the presence of a relatively large cervical mass that was sampled. Under the preliminary diagnosis of large cell non-keratinizing squamous cell carcinoma, the patient underwent radical surgery. Postoperative pathological examination confirmed the diagnosis of HS of the uterine cervix. The patient received chemotherapy.

Conclusion. Clinical presentations of HS of the uterine cervix are very similar to more common cervical tumors; as a result its diagnosis relies on immunohistochemical methods. A correct diagnose could lead to the proper and timely treatment.

DOI: https://doi.org/10.1515/rjim-2016-0051 | Journal eISSN: 2501-062X | Journal ISSN: 1220-4749
Language: English
Page range: 53 - 56
Submitted on: Jul 21, 2016
Published on: Mar 4, 2017
Published by: N.G. Lupu Internal Medicine Foundation
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2017 Fariba Binesh, Mojgan Karimi-Zarchi, Mohammad Reza Vahidfar, Zahra Kargar Hadgiabadi, published by N.G. Lupu Internal Medicine Foundation
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.