Pauls Mehrnoosh, MacKenzie Heather, Ramjeesingh Ravi
Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Medicine, QE2 Health Science Center, Halifax, Nova Scotia, Canada.
BMJ Case Rep. 2019 Jan 10;12(1):bcr-2018-226454. doi: 10.1136/bcr-2018-226454.
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.
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。