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表现为假性梅格斯综合征罕见病例的水肿性平滑肌瘤:文献综述及1例CA125升高的酷似卵巢癌的假性梅格斯综合征病例

Hydropic leiomyoma presenting as a rare condition of pseudo-Meigs syndrome: literature review and a case of a pseudo-Meigs syndrome mimicking ovarian carcinoma with elevated CA125.

作者信息

Pauls Mehrnoosh, MacKenzie Heather, Ramjeesingh Ravi

机构信息

Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.

Medicine, QE2 Health Science Center, Halifax, Nova Scotia, Canada.

出版信息

BMJ Case Rep. 2019 Jan 10;12(1):bcr-2018-226454. doi: 10.1136/bcr-2018-226454.

Abstract

The clinical scenario of a female patient with a pelvic mass, elevated CA125 tumour marker, pleural effusion and ascites is often associated with malignancy. However, not all cases are malignant. Non-malignant diseases, such as Meigs syndrome and pseudo-Meigs syndrome, must be part of your differential. We present a 56-year-old woman with dyspnoea secondary to a right pleural effusion. After further investigations, a serum cancer antigen-125 was found to be elevated at 437.3 U/mL. CT of her abdomen and pelvis showed a large heterogeneous mass in the pelvis measuring 13.2×9.7×15.1 cm with mild ascites. She was initially thought to have ovarian carcinoma and underwent total abdominal hysterectomy and bilateral salpingo-oophorectomy with omental biopsy. Pathology from the surgical specimen revealed a hydropic leiomyoma and after removal of pelvic mass her pleural effusion and ascites completely resolved. She was ultimately diagnosed with the rare pseudo-Meigs syndrome.

摘要

一名患有盆腔肿块、CA125肿瘤标志物升高、胸腔积液和腹水的女性患者的临床情况通常与恶性肿瘤有关。然而,并非所有病例都是恶性的。非恶性疾病,如梅格斯综合征和假性梅格斯综合征,必须纳入你的鉴别诊断。我们报告一名56岁女性,因右侧胸腔积液继发呼吸困难。进一步检查后,发现血清癌抗原125升高至437.3 U/mL。她的腹部和盆腔CT显示盆腔有一个大的不均匀肿块,大小为13.2×9.7×15.1 cm,伴有轻度腹水。她最初被认为患有卵巢癌,并接受了全腹子宫切除术、双侧输卵管卵巢切除术和网膜活检。手术标本的病理显示为水肿性平滑肌瘤,切除盆腔肿块后,她的胸腔积液和腹水完全消退。她最终被诊断为罕见的假性梅格斯综合征。

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本文引用的文献

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