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

IF 1 Q3 MEDICINE, GENERAL & INTERNAL American Journal of Case Reports Pub Date : 2024-07-17 DOI:10.12659/AJCR.943787
Spogmai Khan, Adnan Malik, Shahbaz Qureshi, Babak Cohen, Abdul Nadir
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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.

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肝移植手术中意外诊断出恶性腹膜间皮瘤:病例报告
背景 恶性腹膜间皮瘤(MPM)是一种罕见的致命性浆膜肿瘤。据报道,与 MPM 相关的最常见因素是石棉暴露,同时也有病毒感染、遗传易感性、副肿瘤综合征和免疫力改变的描述。对于肿瘤负担较轻且无特异性症状的患者,诊断可能具有挑战性,偶然发现诊断结果的情况也并不罕见。病例报告 一位患有失代偿期肝硬化的中年女性在移植前接受了广泛的检查,未发现恶性肿瘤的证据。她个人有石棉接触史,家族中有多发性骨髓瘤病史。移植手术期间,她发现腹膜上有几个结节,因此终止了手术。病理分析证实为恶性 MPM。由于腹膜切除术和腹腔内化疗导致肝功能失代偿恶化的风险较高,经多学科讨论后,决定采取保守治疗方法,不进行任何干预。肝移植手术流产后 6 个月,患者的肝功能失代偿症状缓解。自确诊为 MPM 后,正电子发射断层扫描显示 MPM 已连续 3 年未复发。结论 这是首例在肝移植手术中意外诊断出 MPM 的病例。该病例凸显了失代偿期肝病患者中 MPM 诊断和管理所面临的挑战。采用多学科方法并遵照共识决定延长了该患者的生存期。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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