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一例宫颈癌放疗后发生的腹膜恶性间皮瘤。

A case of peritoneal malignant mesothelioma following radiation therapy for cervical cancer.

作者信息

Yano Mitsutake, Ikeda Yuji, Kato Tomomi, Sakaki Mika, Sato Sho, Yabuno Akira, Kozawa Eito, Yasuda Masanori

机构信息

Department of Pathology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.

Department of Gynecologic Oncology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.

出版信息

Mol Clin Oncol. 2018 Feb;8(2):302-305. doi: 10.3892/mco.2017.1525. Epub 2017 Dec 6.

DOI:10.3892/mco.2017.1525
PMID:29435293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5776420/
Abstract

The present study presents a case of peritoneal malignant mesothelioma (PMM) following radiation therapy for cervical cancer. A 34-year-old Japanese woman, without asbestos exposure, was referred to the Department of Gynecologic Oncology, Saitama Medical University International Medical Center due to a cervical mass, and was diagnosed with cervical squamous cell carcinoma (SCC). The serum levels of tumor markers, including SCC antigen and cancer antigen 125 (CA125) were 229.0 ng/ml and 54.4 U/ml, respectively. The patient underwent concurrent chemoradiotherapy (CCRT), and a complete response was achieved. After 54 months, ascites was found at the rectouterine pouch, but peritoneal cytology suggested reactive mesothelial cell. After 62 months of CCRT, magnetic resonance imaging revealed masses in both the salpinges. The serum levels of SCC and CA125 were 0.9 ng/ml and 506.1 U/ml, respectively. Following this, left salpingectomy and peritoneal biopsy were performed laparoscopically. Histologic examination revealed atypical mesothelial cells with no continuity of background tubal epithelium. Immunohistochemistry showed positive staining for calretinin, thrombomodulin, mesothelin and glucose transporter 1. Based on these findings, the patient was diagnosed with PMM epithelioid type and underwent systemic chemotherapy; stable disease status has been obtained for 3 months. This case demonstrates the possibility of PMM occurrence within 10 years after radiotherapy, and indicates the importance of histological and immunohistochemical examination, particularly in cases of an atypical tumorigenesis pattern from the primary cancer.

摘要

本研究报告了一例宫颈癌放疗后发生的腹膜恶性间皮瘤(PMM)。一名34岁无石棉接触史的日本女性因宫颈肿物被转诊至埼玉医科大学国际医疗中心妇科肿瘤科,被诊断为宫颈鳞状细胞癌(SCC)。包括SCC抗原和癌抗原125(CA125)在内的肿瘤标志物血清水平分别为229.0 ng/ml和54.4 U/ml。该患者接受了同步放化疗(CCRT),并取得了完全缓解。54个月后,在直肠子宫陷凹发现腹水,但腹膜细胞学提示为反应性间皮细胞。CCRT 62个月后,磁共振成像显示双侧输卵管有肿物。SCC和CA125的血清水平分别为0.9 ng/ml和506.1 U/ml。此后,通过腹腔镜进行了左侧输卵管切除术和腹膜活检。组织学检查发现非典型间皮细胞,背景输卵管上皮无连续性。免疫组织化学显示钙视网膜蛋白、血栓调节蛋白、间皮素和葡萄糖转运蛋白1呈阳性染色。基于这些发现,该患者被诊断为上皮样型PMM,并接受了全身化疗;目前疾病稳定状态已维持3个月。本病例证明了放疗后10年内发生PMM的可能性,并表明了组织学和免疫组织化学检查的重要性,特别是在原发性癌症出现非典型肿瘤发生模式的情况下。