首页> 外文期刊>Journal of Medical Case Reports >Sarcoidosis in a 65-year-old woman presenting with a lung mass and pericardial effusion: a case report
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Sarcoidosis in a 65-year-old woman presenting with a lung mass and pericardial effusion: a case report

机译:一名65岁女性出现结节病并伴有肺部肿块和心包积液:一例病例报告

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Introduction Sarcoidosis is a multi-systemic disorder of unknown origin and most commonly affects the lungs. Diagnosis relies on the presence of non-caseating granulomas on histologic specimens. In high-resolution computed tomography, the most characteristic findings are peribronchovascular thickening, perilymphatic nodular distribution, and bilateral hilar adenopathy. Confluent nodular opacities or large masses are rare manifestations of the disease. It is well recognized that sarcoidosis can mimic infectious, malignant, and granulomatous conditions. Here, we report a case with a high initial index of suspicion for lung malignancy in terms of clinical, lung imaging, and endoscopic findings. Case presentation A 65-year-old Caucasian woman, lifelong non-smoker with an unremarkable medical history, presented with a 10-month history of progressive breathlessness, dry cough, fatigue, arthralgias, and mild weight loss. The only significant clinical finding was bilateral enlargement of auxiliary lymph nodes. High-resolution computed tomography revealed a soft tissue density mass at the right hilum which was surrounding and narrowing airways and vascular components, nodules with vascular distribution, enlarged mediastinal lymph nodes, and pericardial effusion. Our patient underwent a bronchoscopy, which revealed the presence of submucosal infiltration and narrowing of the right upper bronchus. Endobronchial biopsies showed non-caseating granulomas. As local sarcoid reactions with non-caseating granulomas can be observed near tumors, our patient underwent video-assisted thoracoscopy and surgical removal of an auxiliary lymph node, both of which confirmed the presence of non-caseating granulomas and the diagnosis of sarcoidosis. She was treated with steroids with improvement of clinical and imaging findings. However, while on a maintenance dose, she presented with a pleural effusion, which, after the diagnostic work-up, proved to be sarcoidosis-related. Treatment with initially high doses of steroids plus a steroid-sparing agent led to resolution of the effusion. Conclusions We report a case with a high initial index of suspicion for lung malignancy. Clinicians should always be aware that sarcoidosis enters the differential diagnosis of patients presenting with a lung mass that encases and narrows bronchial and vascular structures with associated pericardial effusion. Rarely, pleural effusion can be the presenting symptom of disease relapse despite maintenance treatment.
机译:简介结节病是一种多系统性疾病,来源不明,最常见于肺部。诊断依赖于组织学标本上存在非干酪性肉芽肿。在高分辨率计算机断层扫描中,最典型的发现是支气管周围血管增厚,淋巴结节状分布和双侧肺门淋巴结肿大。结节混浊或大量肿块是该病的罕见表现。众所周知,结节病可以模仿传染性,恶性和肉芽肿性疾病。在这里,我们报告了一个在临床,肺部影像学和内窥镜检查结果方面怀疑肺癌的初始指标较高的病例。病例介绍一名65岁的白种女人,终生不吸烟,病史不明显,表现为进行性呼吸困难,干咳,疲劳,关节痛和轻度减轻的10个月病史。唯一重要的临床发现是双侧辅助淋巴结肿大。高分辨率计算机断层扫描显示右肺门周围的软组织密度肿块,周围和狭窄的气道和血管成分,结节具有血管分布,纵隔淋巴结肿大和心包积液。我们的患者进行了支气管镜检查,发现粘膜下浸润和右上支气管狭窄。支气管内活检显示非干酪性肉芽肿。由于在肿瘤附近可以观察到非干酪样肉芽肿的局部结节样反应,我们的患者接受了电视胸腔镜检查和辅助淋巴结的手术切除,这两者均证实了非干酪样肉芽肿的存在和结节病的诊断。她接受了激素治疗,临床和影像学检查均得到改善。但是,在维持剂量的同时,她出现了胸腔积液,经诊断后证明与结节病有关。最初使用大剂量的类固醇加类固醇节省剂进行治疗可解决积液。结论我们报告了一例怀疑肺恶性程度较高的病例。临床医生应始终意识到,结节病进入了对肺部肿物的鉴别诊断,肺部肿物包裹并缩小了支气管和血管结构并伴有心包积液。尽管维持治疗,但很少有胸腔积液是疾病复发的症状。

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