Clinical and pathological observation of conversion therapy for malignant peritoneal mesothelioma: a case report and literature review

Minying Deng, Xinyi Zhang, Chen Xu, Rongkui Luo, Lingli Chen, Yuhong Zhou, Yingyong Hou
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Abstract

Background: Malignant mesothelioma (MM) is a tumor originating from the pleura, peritoneum, or pericardial cavity. It is divided into diffuse and localized malignant mesothelioma, with four subtypes in diffuse MM: epithelioid, sarcomatoid, desmoplastic, and biphasic, with biphasic being less common. The onset of this tumor is insidious, and the prognosis is extremely poor in some cases, with a median survival of 6–18 months and no standard treatment options in the past.Aims: We report a case of peritoneal malignant mesothelioma that was successfully treated with transformative therapy. We also review the literature in the hope of providing reference for the treatment and pathological diagnosis of such patients.Methods: The case of the peritoneal malignant mesothelioma was processed and reported in the routine manner for biopsy specimens at different stages.Results and conclusion: We report a case of a malignant tumor originating in the hepatorenal recess, which was diagnosed as biphasic malignant mesothelioma through a biopsy. Immunohistochemical testing showed PD-L1 expression. After multidisciplinary discussion, the patient received transformative treatment, including a trial of combined immunotherapy. The tumor significantly shrank, and the patient obtained a chance for curative surgical resection. Microscopic examination showed significant collagenization in the lesion area, with almost no residual tumor. After 19 months of comprehensive treatment, the patient developed multiple fluffy opacities under the pleura of both lungs. Transthoracic core needle biopsy under CT guidance, the pathology showed organizing pneumonia, considering it as delayed interstitial pneumonitis due to immunotherapy based on previous treatment history. Successful comprehensive treatment was achieved for this case of peritoneal malignant mesothelioma, and the patient has been alive without evidence of disease for 33 months, with long-term follow-up. In this process, the pathologist had three opportunities for pathological diagnosis, which required understanding the patient’s medical history, being attentive to the clinical purpose of the specimen, and providing accurate responses to morphological changes at different stages, along with corresponding descriptions and diagnoses to provide effective information for clinical treatment.
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恶性腹膜间皮瘤转化疗法的临床和病理观察:病例报告和文献综述
背景:恶性间皮瘤(MM)是一种起源于胸膜、腹膜或心包腔的肿瘤。它分为弥漫性和局部性恶性间皮瘤,弥漫性间皮瘤有四个亚型:上皮样型、肉瘤样型、脱瘤型和双相型,其中双相型较少见。该肿瘤起病隐匿,部分病例预后极差,中位生存期仅为6-18个月,过去没有标准治疗方案。目的:我们报告了一例腹膜恶性间皮瘤病例,该病例成功接受了转化疗法。我们还回顾了相关文献,希望能为此类患者的治疗和病理诊断提供参考:方法:对腹膜恶性间皮瘤病例的不同阶段活检标本进行常规处理和报告:我们报告了一例起源于肝肾凹的恶性肿瘤,通过活检诊断为双相恶性间皮瘤。免疫组化检测显示 PD-L1 表达。经过多学科讨论,患者接受了变革性治疗,包括联合免疫疗法试验。肿瘤明显缩小,患者获得了根治性手术切除的机会。显微镜检查显示,病变区域胶原化明显,几乎没有残余肿瘤。综合治疗 19 个月后,患者双肺胸膜下出现多发绒毛状不透明。在 CT 引导下行经胸穿刺活检,病理结果显示为组织性肺炎,根据既往治疗史考虑为免疫治疗导致的迟发性间质性肺炎。这例腹膜恶性间皮瘤患者的综合治疗取得了成功,患者已存活33个月,无疾病迹象,并接受了长期随访。在这个过程中,病理医生有三次病理诊断的机会,需要了解患者的病史,注意标本的临床用途,对不同阶段的形态学变化做出准确的反应,并做出相应的描述和诊断,为临床治疗提供有效的信息。
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