Late Recurrence in Ovarian Dysgerminoma Presenting as a Primary Retroperitoneal Tumor: A Case Report and Review of the Literature

Author:

Sato Yuichiro1ORCID,Hayashi Tohru23,Yamamoto Hidetaka4,Niina Ichiro5,Kuroki Naoya5,Iwamura Takeshi5,Onishi Junji6

Affiliation:

1. Department of Diagnostic Pathology, Miyazaki University Hospital, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan

2. Department of Diagnostic Pathology, Junwakai Memorial Hospital, Komatsu, Miyazaki 880-2112, Japan

3. Department of Clinical Laboratory, Breastopia Miyazaki Hospital, Maruyama, Miyazaki 880-0052, Japan

4. Department of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyusyu University, Umade, Fukuoka 812-8582, Japan

5. Department of Surgery, Junwakai Memorial Hospital, Komatsu, Miyazaki 880-2112, Japan

6. Department of Obstetrics and Gynecology, Faculty of Medicine, University of Miyazaki, Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan

Abstract

Ovarian dysgerminoma is a rare type of germ cell tumor. The majority of patient relapses occur within 2 years of diagnosis. Here, we report the case of a 74-year-old woman with a history of ovarian dysgerminoma 39 years earlier. The patient visited the hospital presenting with heartburn. An abdominal computed tomography (CT) revealed a right retroperitoneal mass, and a primary retroperitoneal tumor was suspected. She underwent surgical resection of the retroperitoneal tumor. Histological examination confirmed a metastatic dysgerminoma to the retroperitoneum. Postoperative CT showed paraaortic and cervical lymph node metastases. The patient was treated with bleomycin, etoposide, and cisplatin chemotherapy. This case demonstrates the difficulties that may be encountered in the differential diagnosis of a retroperitoneal mass and underlines the necessity for understanding a patient’s clinical history.

Publisher

Hindawi Limited

Subject

General Medicine

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