Motegi Yoko, Ogawa Hiroomi, Tateno Kohei, Suga Kunihiko, Okada Takuhisa, Osone Katsuya, Katoh Ryuji, Ogata Kyoichi, Sakai Makoto, Sohda Makoto, Makiguchi Takaya, Shirabe Ken, Saeki Hiroshi
Department of General Surgical Science, Graduate School of Medicine, Gunma University, 3-39-22, Showa-machi, Maebashi Gunma, 371-8511, Japan.
Clinical Department of Pathology, Gunma University Hospital, 3-39-15, Showa-machi, Maebashi Gunma, 371-8511, Japan.
Clin J Gastroenterol. 2021 Aug;14(4):1169-1174. doi: 10.1007/s12328-021-01436-0. Epub 2021 Jun 28.
Retroperitoneal leiomyoma is a very rare disease, with little reported information on its origin. Herein, we report a case of a large retroperitoneal leiomyoma that developed from the pelvic floor. A 44-year-old woman had a large mass protruding outside the body from the right hip. Imaging revealed a large tumor developing from the pelvic floor to the buttocks. It was difficult to identify the place of origin. Upon preoperative biopsy, the patient was diagnosed with retroperitoneal leiomyoma. Tumor removal with abdominoperineal and partial vaginal resection was performed. Based on the histological findings of the surgical specimens, she was diagnosed with a retroperitoneal leiomyoma (gynecologic type) via immunohistochemistry, the tumor cells were positive for αSMA, desmin, estrogen receptor(ER), and progesterone receptor(PgR), but negative for myoglobin, S-100, CD34, and MIB-1.This is a case of a large retroperitoneal leiomyoma that was successfully removed via abdominoperineal and partial vaginal resection.
腹膜后平滑肌瘤是一种非常罕见的疾病,关于其起源的报道信息很少。在此,我们报告一例起源于盆底的巨大腹膜后平滑肌瘤病例。一名44岁女性右髋部有一巨大肿物突出于体外。影像学检查显示一个从盆底延伸至臀部的巨大肿瘤。难以确定其起源部位。术前活检时,患者被诊断为腹膜后平滑肌瘤。行腹会阴联合及部分阴道切除术切除肿瘤。根据手术标本的组织学检查结果,通过免疫组化诊断为腹膜后平滑肌瘤(妇科型),肿瘤细胞αSMA、结蛋白、雌激素受体(ER)和孕激素受体(PgR)呈阳性,但肌红蛋白、S-100、CD34和MIB-1呈阴性。这是一例通过腹会阴联合及部分阴道切除术成功切除的巨大腹膜后平滑肌瘤病例。