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一例伴有系统性红斑狼疮血清学阳性的恶性间皮瘤罕见病例:病例报告及文献综述

A Rare Case of Malignant Mesothelioma Presenting with Systemic Lupus Erythematosus Seropositivity: A Case Report and Review of Literature.

作者信息

Rakhra Amandeep, Munir Ahmed, Chilukuri Ramya S, Nahas Joseph

机构信息

Internal Medicine, Creighton University, Omaha, USA.

Rheumatology, Creighton University, Omaha, USA.

出版信息

Cureus. 2019 Feb 19;11(2):e4092. doi: 10.7759/cureus.4092.

Abstract

While malignant mesothelioma may initially present in a variety of ways, it is uncommon to present with systemic lupus erythematosus (SLE) seropositivity and thus obscuring its diagnosis. Our case involves a 75-year-old Caucasian male with a past medical history of essential hypertension, remote prostate cancer status post prostatectomy, and lifetime nontobacco use presenting with progressive shortness of breath over one month. After a negative cardiac assessment, a postcardiac catheterization chest X-ray (CXR) revealed a right-sided moderate-to-large pleural effusion that, on further workup, was found to be exudative. Effusion studies were negative for malignancy and bacterial growth. Recurrent accumulation of fluid after a thoracentesis one week prior prompted an autoimmune work up. Positive markers included antinuclear antibodies, anti-double stranded DNA antibodies, and anti-histone antibodies, while anti-Smith antibodies were negative. Although SLE was initially suspected based on serologies, no clinical signs or symptoms were present to fulfill the diagnosis criteria. A trial of oral prednisone resulted in decreased pleural effusion size with no further recurrence. Additional studies included a CT scan of the chest that showed pleural masses confirmed with biopsy to be epithelioid mesothelioma. Given the patient's age and new diagnosis of malignant mesothelioma, we hypothesized that the presence of autoantibodies was likely false positives due to acquired autoantibodies with age, hyperactivity of the immune system from malignancy, and possible prior asbestos exposure.

摘要

虽然恶性间皮瘤最初可能有多种表现形式,但出现系统性红斑狼疮(SLE)血清学阳性并因此掩盖其诊断的情况并不常见。我们的病例是一名75岁的白种男性,既往有原发性高血压病史,既往有前列腺癌病史且已行前列腺切除术,终生不吸烟,出现进行性气短1个月。心脏评估阴性后,心脏导管检查后的胸部X线(CXR)显示右侧中到大量胸腔积液,进一步检查发现为渗出性。积液检查未发现恶性肿瘤和细菌生长。1周前胸腔穿刺后液体反复积聚促使进行自身免疫检查。阳性标志物包括抗核抗体、抗双链DNA抗体和抗组蛋白抗体,而抗史密斯抗体为阴性。虽然最初根据血清学怀疑为SLE,但没有符合诊断标准的临床体征或症状。口服泼尼松试验使胸腔积液体积减小且未再复发。其他检查包括胸部CT扫描,显示胸膜肿块,活检证实为上皮样间皮瘤。鉴于患者年龄和新诊断的恶性间皮瘤,我们推测自身抗体的存在可能是由于年龄增长导致的获得性自身抗体、恶性肿瘤引起的免疫系统亢进以及可能既往有石棉暴露而出现的假阳性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c135/6472718/caae33e0cbe1/cureus-0011-00000004092-i01.jpg

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