成年男性良性间充质肝错构瘤1例报告及文献复习。

Acta medica Austriaca Pub Date : 2003-01-01
T Brkic, I Hrstic, B Vucelic, J Jakic-Razumovic, M Skegro, B Romic, S Cukovic-Cavka, R Pulanic, R Ostojic
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引用次数: 0

摘要

肝脏间充质错构瘤是一种罕见的良性病变,几乎只发生在两岁以下的儿童身上。1903年报告了第一例病例,到目前为止报告的病例不到200例。一位38岁男性主诉钝性肋下疼痛持续近10个月,腹部超声检查发现肝脏局灶性病变。他被转到我科,影像学检查(超声和计算机断层扫描)显示一个实性病变,直径8厘米,位于肝脏IVb和V段。病变与胆囊壁之间无明显边界。甲胎蛋白和癌胚抗原在正常范围内,碳水化合物抗原19-9轻微升高。没有转移性疾病的证据。超声引导下对病变进行活检,活检标本病理报告提示肿瘤可能为良性间充质错构瘤。患者接受了正式的双节段切除术(IVb和V节段)和胆囊切除术。最终病理报告证实了良性间充质错构瘤的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Benign mesenchymal liver hamartoma in an adult male: a case report and review of the literature.

Mesenchymal hamartoma of the liver is an uncommon benign lesion seen almost exclusively in children younger than two years of age. The first case was reported in 1903, and until now fewer than 200 cases have been reported. A 38-year-old male complaining of dull subcostal pain lasting for almost 10 months was found on abdominal ultrasound to have a focal lesion of the liver. He was referred to our Unit where imaging procedures (ultrasound and computed tomography) revealed a solid lesion, 8 centimeters in diameter, located in the IVb and V segments of the liver. There were no clear margins between the lesion and the gallbladder wall. Alpha-fetoprotein and carcinoembryonic antigen were within normal limits and carbohydrate antigen 19-9 was minimally elevated. There was no evidence of metastatic disease. Ultrasound-guided biopsy of the lesion was done and pathology report of a biopsy specimen suggested that the tumor was probably a benign mesenchymal hamartoma. The patient underwent a formal bi-segmentectomy (IVb and V segments) with cholecystectomy. Definitive pathology report confirmed the diagnosis of a benign mesenchymal hamartoma.

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