[Analysis of clinicopathological features of 68 cases of malignant pleural mesothelioma]

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2023 Aug 20;41(8):588-593. doi: 10.3760/cma.j.cn121094-20220425-00221.
[Article in Chinese]

Abstract

Objective: To analyze the clinicopathological characteristics of diffuse malignant pleural mesothelioma (MPM), and explore the diagnostic methods in order to improve the early diagnosis rate. Methods: In January 2019 to January 2022, the clinical features, auxiliary examination and immunohistochemical results of 68 cases of MPM were analyzed retrospectively. The pathogenic features, histopathological morphology and the expression of related antibodies including Calretinin (CR), D2-40 and WT-1 were summarized. Results: Among the 68 patients, 40 male (58.82%), 28 female (41.18%), male to female ratio was 1.43%, median age was 58 years old; 50% of patients in Dayao County, epithelial mesothelioma 59 cases (86.76%), occurred in right chest in 39 cases (57.35%), left chest in 25 cases (36.76%), and 4 cases in both sides (5.89%). The most common initial clinical manifestations were pleural effusion (95.59%), chest pain (36.75%), chest tightness and shortness of breath (30.88%). The main imaging findings were pleural effusion in 49 cases (98.00%) and pleural thickening in 46 cases (92.00%). MPM tumor cells often expressed Calretinin, CK5/6, WT1 and D2-40, while TTF-1, NapsinA and CEA, the main markers differentiated from lung adenocarcinoma were negative. Serum CYFRA21-1 and CEA have high value in differential diagnosis of benign and malignant pleural effusions. Conclusion: Diffuse MPM has diverse histological and cytological morphology, which needs to be differentiated from a variety of diseases. Correct diagnosis of diffuse MPM through immunohistochemistry requires the combined application of a group of Mesothelium related antibodies.

目的: 分析弥漫性恶性胸膜间皮瘤(MPM)的临床病理特征,探讨诊断思路,以期提高早期诊断率。 方法: 于2019年1月至2022年1月回顾性研究楚雄彝族自治州人民医院68例MPM患者的临床资料,通过分析其临床特征、辅助检查及免疫组织化学资料,总结其发病特征、组织病理学形态及钙结合蛋白(CR)、肾小球足突细胞膜蛋白(D2-40)、肾母细胞瘤基因-1(WT-1)等表达情况。 结果: 68例患者中,男性40例(58.82%)、女性28例(41.18%),中位年龄为58.0岁。病理类型以上皮型为主59例(86.76%);发生部位以后右侧胸腔为主39例(57.35%)。最常见的首发临床表现为胸腔积液(95.59%)、胸痛(36.75%)、胸闷气促(30.88%),50例患者进行影像学检查主要表现为胸腔积液49例(98.00%),胸膜增厚46例(92.00%)。MPM瘤细胞常表达CR、肾母细胞癌基因-1(WT-1)和D2-40等,与肺腺癌鉴别的主要标志物甲状腺转录因子1(TTF-1)、天冬氨酸蛋白酶A(Napsin A)、癌胚抗原(CEA)阴性。患者血清细胞角蛋白21-1(CYFRA21-1)和CEA对良、恶性胸腔积液具有较高的鉴别诊断价值。 结论: 弥漫型MPM组织学和细胞学形态多样,需要与多种疾病鉴别,通过免疫组化正确诊断弥漫型MPM需一组间皮细胞相关抗体联合应用。.

Keywords: Clinical features; Diagnosis; Immunohistochemistry; Malignant pleural mesothelioma.

Publication types

  • English Abstract

MeSH terms

  • Calbindin 2
  • Female
  • Humans
  • Male
  • Mesothelioma, Malignant*
  • Middle Aged
  • Pleural Effusion*
  • Retrospective Studies

Substances

  • antigen CYFRA21.1
  • Calbindin 2