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肝移植手术中偶然诊断出恶性腹膜间皮瘤:一例报告

Incidental Diagnosis of Malignant Peritoneal Mesothelioma During Liver Transplantation Surgery: A Case Report.

作者信息

Khan Spogmai, Malik Adnan, Qureshi Shahbaz, Cohen Babak, Nadir Abdul

机构信息

Department of Internal Medicine, Mountain Vista Medical Center, Midwestern University, Mesa, AZ, USA.

Division of Gastroenterology, Mountain Vista Medical Center, Midwestern University, Mesa, AZ, USA.

出版信息

Am J Case Rep. 2024 Jul 17;25:e943787. doi: 10.12659/AJCR.943787.

Abstract

BACKGROUND Malignant peritoneal mesothelioma (MPM) is a rare, lethal tumor of serous membranes. The most common factor reported in association with MPM is asbestos exposure, while viral infections, genetic predisposition, paraneoplastic syndrome, and altered immunity have been described as well. The diagnosis can be challenging among those with lower tumor burden as well as nonspecific symptoms, and it is not unusual to discover the diagnosis incidentally. CASE REPORT A middle-aged woman with decompensated cirrhosis underwent extensive pre-transplant workup, showing no evidence of malignancy. She had a personal history of asbestos exposure and family history of MPM in the extended family. During transplant surgery, a few peritoneal nodules were noted, leading to termination of the procedure. Pathological analysis confirmed malignant MPM. A multidisciplinary discussion led to following a conservative treatment approach without any intervention, due to higher risk of worsening hepatic decompensation associated with peritonectomy and intraperitoneal chemotherapy. The patient's hepatic decompensation resolved 6 months after the aborted liver transplant operation. Since the diagnosis of MPM, positron emission tomography scans have shown no recurrence of MPM for 3 consecutive years. CONCLUSIONS This is the first case of MPM diagnosed incidentally during a liver transplantation surgery. This case highlights the challenges in the diagnosis and management of MPM in a patient with decompensated liver disease. A multidisciplinary approach and following a consensus decision led to prolonged survival in the described patient.

摘要

背景

恶性腹膜间皮瘤(MPM)是一种罕见的浆膜致死性肿瘤。与MPM相关的最常见因素是石棉暴露,同时也描述了病毒感染、遗传易感性、副肿瘤综合征和免疫改变等因素。在肿瘤负荷较低以及症状不特异的患者中,诊断可能具有挑战性,偶然发现诊断并不罕见。

病例报告

一名失代偿期肝硬化的中年女性在移植前进行了全面检查,未发现恶性肿瘤证据。她有石棉暴露个人史,大家庭中有MPM家族史。在移植手术过程中,发现了一些腹膜结节,导致手术终止。病理分析证实为恶性MPM。多学科讨论后,由于与腹膜切除术和腹腔内化疗相关的肝失代偿恶化风险较高,决定采取保守治疗方法,不进行任何干预。在中止肝移植手术后6个月,患者的肝失代偿得到缓解。自诊断为MPM以来,正电子发射断层扫描显示MPM连续3年未复发。

结论

这是首例在肝移植手术中偶然诊断出MPM的病例。该病例凸显了在失代偿性肝病患者中MPM诊断和管理的挑战。多学科方法和遵循共识决定使所述患者获得了延长生存期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d32/11304631/9f0048bf60e8/amjcaserep-25-e943787-g001.jpg

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