A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass
Histiocytic cell malignancies are very rare. Hence, the information about this disease in hematology is limited. In this case report, we present a case of malignant histiocytic tumor affecting the ovary of a 40-year-old virgin female. Primary ovarian malignancy was not considered for the patient who...
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Wiley
2018-01-01
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Series: | Case Reports in Obstetrics and Gynecology |
Online Access: | http://dx.doi.org/10.1155/2018/1792358 |
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author | Emsal Pinar Topdagi Yilmaz Yakup Kumtepe Yunus Emre Topdagi Seray Kaya Topdagi |
author_facet | Emsal Pinar Topdagi Yilmaz Yakup Kumtepe Yunus Emre Topdagi Seray Kaya Topdagi |
author_sort | Emsal Pinar Topdagi Yilmaz |
collection | DOAJ |
description | Histiocytic cell malignancies are very rare. Hence, the information about this disease in hematology is limited. In this case report, we present a case of malignant histiocytic tumor affecting the ovary of a 40-year-old virgin female. Primary ovarian malignancy was not considered for the patient who was approached as if she had ovarian malignancy, since there was an indication of a mass in the ovary. Therefore, an aggressive surgery was not performed. Since our patient was in the reproductive age, fertility-preserving surgery was performed. Our patient was then treated systemically by medical oncology. In conclusion, the rare malignancy group was investigated in the present study along with an evaluation of the current literature. |
format | Article |
id | doaj-art-e742fe08405d4e24b84cf7880ec6e030 |
institution | Kabale University |
issn | 2090-6684 2090-6692 |
language | English |
publishDate | 2018-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Obstetrics and Gynecology |
spelling | doaj-art-e742fe08405d4e24b84cf7880ec6e0302025-02-03T05:46:05ZengWileyCase Reports in Obstetrics and Gynecology2090-66842090-66922018-01-01201810.1155/2018/17923581792358A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian MassEmsal Pinar Topdagi Yilmaz0Yakup Kumtepe1Yunus Emre Topdagi2Seray Kaya Topdagi3Department of Gynecology and Obstetrics, Atatürk University School of Medicine, Erzurum, TurkeyDepartment of Gynecology and Obstetrics, Atatürk University School of Medicine, Erzurum, TurkeyClinic of Gynecology and Obstetrics, Nene Hatun Gynecology and Obstetrics Hospital, Erzurum, TurkeyDepartment of Gynecology and Obstetrics, Atatürk University School of Medicine, Erzurum, TurkeyHistiocytic cell malignancies are very rare. Hence, the information about this disease in hematology is limited. In this case report, we present a case of malignant histiocytic tumor affecting the ovary of a 40-year-old virgin female. Primary ovarian malignancy was not considered for the patient who was approached as if she had ovarian malignancy, since there was an indication of a mass in the ovary. Therefore, an aggressive surgery was not performed. Since our patient was in the reproductive age, fertility-preserving surgery was performed. Our patient was then treated systemically by medical oncology. In conclusion, the rare malignancy group was investigated in the present study along with an evaluation of the current literature.http://dx.doi.org/10.1155/2018/1792358 |
spellingShingle | Emsal Pinar Topdagi Yilmaz Yakup Kumtepe Yunus Emre Topdagi Seray Kaya Topdagi A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass Case Reports in Obstetrics and Gynecology |
title | A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass |
title_full | A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass |
title_fullStr | A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass |
title_full_unstemmed | A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass |
title_short | A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass |
title_sort | rare case report a malignant histiocytic tumor in the form of ovarian mass |
url | http://dx.doi.org/10.1155/2018/1792358 |
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