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一名42岁女性系统性红斑狼疮合并恶性胸膜间皮瘤病例

A Case of Systemic Lupus Erythematosus with Malignant Pleural Mesothelioma in a 42-year Woman.

作者信息

Liu Yunyun, Tong Jianlin, Ling Xuefeng, Cao Wa, Fang Lei

机构信息

Department of Pneumology, The Affiliated Hospital of Jiujiang University, Jiangxi Province, China.

出版信息

J Coll Physicians Surg Pak. 2020 Oct;30(10):1099-1101. doi: 10.29271/jcpsp.2020.10.1099.

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune connective tissue disease characterised by inflammation. Malignant pleural mesothelioma (MPM) is a highly invasive malignant tumor derived from pleural mesothelial cells. Here, we report a case of SLE with MPM. A 42-year woman with no exposure to asbestos presented with severe left chest pain. Initially, we diagnosed her with SLE because of the clinical manifestations and high antinuclear antibody titer. Finally, a diagnosis of MPM was made, based on pleural biopsy. Her condition was under control after one cycle of chemotherapy and oral methotrexate. However, three years later, she was admitted with dyspnea, mild orthopnea, and tachycardia, and died one month later after discontinuing treatment. MPM is rare, and MPM with SLE is even rarer. We should pay attention to pleural effusion when diagnosing SLE. If possible, a pleural biopsy should be performed to reduce misdiagnosis and missed diagnosis. Key Words: Pleural effusion, Systemic lupus erythematosus (SLE), Mesothelioma.

摘要

系统性红斑狼疮(SLE)是一种以炎症为特征的自身免疫性结缔组织病。恶性胸膜间皮瘤(MPM)是一种源自胸膜间皮细胞的高度侵袭性恶性肿瘤。在此,我们报告一例合并MPM的SLE病例。一名42岁未接触过石棉的女性出现严重左胸痛。最初,由于临床表现和高抗核抗体滴度,我们诊断她为SLE。最终,基于胸膜活检确诊为MPM。经过一个周期的化疗和口服甲氨蝶呤后,她的病情得到控制。然而,三年后,她因呼吸困难、轻度端坐呼吸和心动过速入院,停止治疗一个月后死亡。MPM罕见,合并SLE的MPM更为罕见。诊断SLE时我们应注意胸腔积液。如有可能,应进行胸膜活检以减少误诊和漏诊。关键词:胸腔积液、系统性红斑狼疮(SLE)、间皮瘤

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