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由快速增大的水肿性平滑肌瘤伴CA125水平升高引起的假性梅格斯综合征,酷似卵巢恶性肿瘤:一例报告及文献复习

Pseudo-Meigs syndrome caused by a rapidly enlarging hydropic leiomyoma with elevated CA125 levels mimicking ovarian malignancy: a case report and literature review.

作者信息

Zou Longquan, Lou Jinlong, Huang Haoran, Xu Lian

机构信息

Department of Pathology, Zigong Fourth People's Hospital, Zigong, Sichuan, China.

Institute of Precision Medicine, Zigong Academy of Medical Big Data and Artificial Intelligence, Zigong, Sichuan, China.

出版信息

BMC Womens Health. 2024 Aug 7;24(1):445. doi: 10.1186/s12905-024-03285-8.

Abstract

Pseudo-Meigs syndrome is a rare syndrome characterized by hydrothorax and ascites associated with pelvic masses, and patients occasionally present with elevated serum cancer antigen-125 (CA125) levels. Hydropic leiomyoma (HLM) is an uncommon subtype of uterine leiomyoma characterized by hydropic degeneration and secondary cystic changes. Rapidly enlarging HLMs accompanied by hydrothorax, ascites, and elevated CA125 levels may be misdiagnosed as malignant tumors. Here, we report a case of HLM in a 45-year-old Chinese woman who presented with ascites and hydrothorax. Preoperative abdominopelvic CT revealed a giant solid mass in the fundus uteri measuring 20 × 15 × 12 cm. Her serum CA125 level was elevated to 247.7 U/ml, while her hydrothorax CA125 level was 304.60 U/ml. The patient was initially diagnosed with uterine malignancy and underwent total abdominal hysterectomy and adhesiolysis. Pathological examination confirmed the presence of a uterine hydropic leiomyoma with cystic changes. After tumor removal, the ascites and hydrothorax subsided quickly, with no evidence of recurrence. The patient's serum CA125 level decreased to 116.90 U/mL on Day 7 and 5.6 U/mL on Day 40 postsurgery. Follow-up data were obtained at 6 months, 1 year, and 2 years after surgery, and no recurrence of ascites or hydrothorax was observed. This case highlights the importance of accurate diagnosis and appropriate management of HLM to achieve successful outcomes.

摘要

假性梅格斯综合征是一种罕见综合征,其特征为胸腔积液、腹水伴盆腔肿块,患者血清癌抗原125(CA125)水平偶尔会升高。水肿性平滑肌瘤(HLM)是子宫平滑肌瘤的一种罕见亚型,其特征为水肿性退变和继发性囊性改变。迅速增大的HLM伴有胸腔积液、腹水及CA125水平升高,可能会被误诊为恶性肿瘤。在此,我们报告一例45岁中国女性的HLM病例,该患者表现为腹水和胸腔积液。术前腹盆腔CT显示子宫底部有一个巨大实性肿块,大小为20×15×12cm。她的血清CA125水平升高至247.7U/ml,而胸腔积液中的CA125水平为304.60U/ml。患者最初被诊断为子宫恶性肿瘤,并接受了全腹子宫切除术和粘连松解术。病理检查证实存在伴有囊性改变的子宫水肿性平滑肌瘤。肿瘤切除后,腹水和胸腔积液迅速消退,无复发迹象。术后第7天患者血清CA125水平降至116.90U/mL,术后第40天降至5.6U/mL。在术后6个月、1年和2年获得随访数据,未观察到腹水或胸腔积液复发。该病例突出了准确诊断和恰当处理HLM以取得成功治疗效果的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c29/11304927/2f35f2cd35cf/12905_2024_3285_Fig1_HTML.jpg

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