Epithelioid Angiosarcoma Arising from a Huge Leiomyoma: A Case Report and a Literature Review. 2018

Takeya Hara, and Ai Miyoshi, and Yuji Kamei, and Nao Wakui, and Akiko Fujishiro, and Serika Kanao, and Hirokazu Naoi, and Hirofumi Otsuka, and Takeshi Yokoi
Department of Obstetrics and Gynecology, Kaizuka City Hospital, Osaka, Japan.

Uterine mesenchymal tumors other than leiomyosarcoma, carcinosarcoma, and endometrial stromal sarcomas are extremely uncommon. We describe a case of epithelioid angiosarcoma of the uterus and review previous literature on such rare tumors. A 48-year-old woman presented with a 1-year history of abdominal fullness and 10kg weight loss. Pelvic magnetic resonance imaging (MRI) revealed a huge (30×18cm) uterus accompanied by degeneration and necrosis. She underwent supracervical hysterectomy and right salpingo-oophorectomy. We postoperatively diagnosed the mass as an epithelioid angiosarcoma arising from a leiomyoma. Vasodilatation was observed within the range of 2 cm × several mm in the leiomyoma, and proliferation of atypical cells was observed covering the surface of the luminal side. The tumor showed a partly fine vascular structure and was associated with obvious nuclear atypia and mitotic figures. She received 6 courses of adjuvant chemotherapy with paclitaxel, epirubicin, and carboplatin, and there have been no signs of recurrence for 10 months.

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