Uterine myxoid leiomyosarcoma with tumor embolism extending into the right atrium: A case Report

Hiromi Imai, hiroshi yagi, Okugawa Kaoru, Hironori Kenjo, Tatsuhiro Ohgami, Yoshiaki Kawano, Kaneki Eisuke, Akimasa Ichinoe, Kazuo Asanoma, Hideaki Yahata, Kenzo Sonoda, Hiroaki Kobayashi, Tsunehisa Kaku, Kiyoko Kato

研究成果: Contribution to journalArticle査読

抄録

Uterine myxoid leiomyosarcoma (MLMS) is an extremely rare variant of uterine leiomyosarcoma; only 56 cases were reported from 1982 to 2013. Uterine MLMS is characterized by a myxoid appearance and highly malignant behavior. We herein report a case involving a 65-year-old woman with uterine MLMS with a large tumor embolism that reached the right atrium. A total abdominal hysterectomy, bilateral salpingooophorectomy, and tumor embolism resection with the use of a heart-lung machine were performed. Epirubicin-ifosfamide chemotherapy in the adjuvant setting led to reductions in both the tumor emboli and peritoneal dissemination. The patient retained a good quality of life for 10 months after the initial surgery. She then developed progressive disease despite treatment with pazopanib. She died of her disease 14 months after the initial surgery. Although complete surgical resection of the tumor is desirable, tumor reduction surgery followed by adjuvant chemotherapy might help to retain a good quality of life. This is the first reported case of a primary uterine MLMS with tumor emboli.
本文言語英語
論文番号316262
ページ数5
ジャーナルCase Reports in Obstetrics and Gynecology
2015
出版ステータス印刷前のE-pub - 2 2 2015

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