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原发性卵巢平滑肌肉瘤

Primary ovarian leiomyosarcoma.

作者信息

Zygouris D, Androutsopoulos G, Grigoriadis C, Arnogiannaki N, Terzakis E

机构信息

2nd Department of Gynaecology, St. Savvas Anticancer-Oncologic Hospital, Athens, Greece.

出版信息

Eur J Gynaecol Oncol. 2012;33(3):331-3.

Abstract

BACKGROUND

Primary ovarian leiomyosarcoma is an extremely rare subtype of ovarian sarcomas. It most commonly occurs in postmenopausal women and has unfavorable prognosis.

CASE

The patient, a 58-year-old postmenopausal woman, presented with a complaint of abdominal pain. Preoperative examination revealed an intraabdominal mass 25 x 17 x 14 cm in the right adnexa. She underwent bilateral salpingo-oophorectomy, total omentectomy, appendectomy and bilateral pelvic lymphadenectomy. The histopathology revealed leiomyosarcoma of the right ovary Stage Ia. She did not receive any postoperative adjuvant therapy. Follow-up 21 months after initial surgery, showed no evidence of recurrence.

CONCLUSION

Additional studies are needed to understand more about the nature, clinical behavior and treatment of this very rare tumor.

摘要

背景

原发性卵巢平滑肌肉瘤是卵巢肉瘤中极其罕见的一种亚型。它最常发生于绝经后女性,预后不佳。

病例

该患者为一名58岁绝经后女性,主诉腹痛。术前检查发现右附件区有一个25×17×14 cm的腹腔内肿块。她接受了双侧输卵管卵巢切除术、全大网膜切除术、阑尾切除术和双侧盆腔淋巴结清扫术。组织病理学检查显示为右卵巢Ia期平滑肌肉瘤。她未接受任何术后辅助治疗。初次手术后21个月的随访显示无复发迹象。

结论

需要更多研究以进一步了解这种非常罕见肿瘤的性质、临床行为和治疗方法。

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