Malignant Mesothelioma Extending from Peritoneum to Pleura: A Diagnostic Challenge and Case Report.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2026-04-27 eCollection Date: 2026-01-01 DOI:10.1159/000551912
Thanh Thuy Phan, Thi Quynh Huong Pham, Van Duy Le, Thi Lan Tran, Van Chuong Tran, Nguyen Thị Hoa Mai, Thu Phuong Phan, Van Giap Vu
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Abstract

Introduction: Sarcomatoid malignant peritoneal mesothelioma (SM-MPM) is an exceptionally rare and aggressive subtype of peritoneal mesothelioma, often presenting with nonspecific symptoms such as ascites. Due to its subtle clinical manifestations, diagnosis is frequently delayed, resulting in poor prognosis. Early and accurate identification is crucial for guiding appropriate therapeutic strategies.

Case presentation: We report the case of a 52-year-old woman with no history of smoking, alcohol use, or asbestos exposure, who previously underwent subtotal hysterectomy for uterine fibroids in 2017. Ten months prior to admission, she developed progressive abdominal distension, fatigue, and ascites, accompanied by elevated CA-125 levels. Initial symptomatic improvement was achieved with diuretics, but no definitive diagnosis was established. Eight months later, she was readmitted with recurrent ascites, chest tightness, and dyspnea. Imaging revealed right pleural effusion, pneumothorax, and peritoneal thickening. Pleuroscopic biopsy showed reactive mesothelial proliferation. One month into hospitalization, rapid re-accumulation of ascitic fluid prompted repeat imaging, which demonstrated irregular peritoneal thickening and nodularity. Laparoscopic peritoneal biopsy with immunohistochemistry confirmed the diagnosis of SM-MPM. The disease was staged as T3N0M1 based on the Peritoneal Cancer Index (PCI), indicating advanced disease with poor prognosis. The patient was referred to a specialized oncology center for further management.

Conclusions: This case underscores the diagnostic challenges of SM-MPM, particularly in patients presenting with recurrent unexplained ascites and multiple serous effusions. It highlights the importance of maintaining a high index of suspicion and the pivotal role of laparoscopy, immunohistochemistry, and multidisciplinary collaboration in achieving timely diagnosis and optimizing patient outcomes.

恶性间皮瘤从腹膜延伸到胸膜:一个诊断挑战和病例报告。
肉瘤样恶性腹膜间皮瘤(SM-MPM)是一种非常罕见的侵袭性腹膜间皮瘤亚型,通常表现为非特异性症状,如腹水。由于其临床表现不明显,常常延误诊断,导致预后不良。早期和准确的识别对于指导适当的治疗策略至关重要。病例介绍:我们报告了一名52岁的女性,无吸烟、饮酒或石棉暴露史,曾于2017年因子宫肌瘤接受子宫次全切除术。入院前10个月,患者出现进行性腹胀、疲劳和腹水,并伴有CA-125水平升高。最初使用利尿剂可以改善症状,但没有明确的诊断。8个月后,因反复腹水、胸闷、呼吸困难再次入院。影像显示右侧胸腔积液、气胸及腹膜增厚。胸膜镜活检显示反应性间皮增生。住院1个月后,腹水迅速重新积聚,提示重复成像,显示不规则腹膜增厚和结节。腹腔镜腹膜活检和免疫组织化学证实了SM-MPM的诊断。根据腹膜癌指数(PCI)分期为T3N0M1,提示病情进展,预后较差。病人被转诊到专门的肿瘤中心接受进一步治疗。结论:该病例强调了SM-MPM的诊断挑战,特别是在出现复发性不明原因腹水和多发浆液积液的患者中。它强调了保持高怀疑指数的重要性,以及腹腔镜检查、免疫组织化学和多学科合作在实现及时诊断和优化患者预后方面的关键作用。
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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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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