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以复发性大量胸腔积液为首发表现的结节病:1 例报告。

Rapidly recurring massive pleural effusion as the initial presentation of sarcoidosis: A case report.

机构信息

Internal Medicine Department, Hamad Medical Corporation, Doha, Qatar.

出版信息

Medicine (Baltimore). 2021 Feb 12;100(6):e24027. doi: 10.1097/MD.0000000000024027.

Abstract

RATIONALE

Sarcoidosis is a multisystem granulomatous disease with unknown etiology. It affects mainly the lungs, but it can affect almost any other organ. Nevertheless, pleural involvement with the development of pleural effusion is relatively rare. It is usually mild and responsive to treatment with systemic steroids. Here we present a case of rapidly recurring massive unilateral pleural effusion caused by sarcoidosis that was resistant to systemic steroids.

PATIENT CONCERNS

A 55-year-old lady presented with shortness of breath of 2-months duration. No other respiratory symptoms were reported. On physical examination, there were signs of left-sided pleural effusion, splenomegaly, and inguinal lymph nodes. These findings were confirmed by chest x-ray showing massive pleural effusion. Work up of the effusion revealed an exudative effusion with lymphocyte predominance. Pan-computed tomography scan revealed multiple thoracic, abdominal and inguinal lymphadenopathy; additionally, a left-sided pleural effusion and an enlarged spleen; that contained variable hypodense nodular lesions. Positron emission tomography-computed tomography showed intense uptake in the spleen and the lymph nodes. Inguinal lymph node biopsy showed non-necrotizing granulomatous inflammation. Due to suspicion of malignancy, left medical thoracoscopy was done, and biopsy of the parietal pleura showed nonspecific inflammation without evidence of malignancy or tuberculosis.

DIAGNOSIS

Sarcoidosis was diagnosed based on the finding of the non-necrotizing granulomatous inflammation with no evidence of malignancy or infection on several microbiological and pathological samples.

INTERVENTIONS

The patient was treated with repeated pleural fluid drainage. Steroids failed to prevent pleural effusion recurrence. Surgical left side pleurodesis was eventually performed.

OUTCOMES

At more than 1 year follow up, the patient showed no recurrence of pleural effusion or development of any other symptoms.

LESSONS

Sarcoidosis may rarely present with massive pleural effusion, as this presentation is rare; it is imperative to rule out other causes of massive pleural effusion. Massive pleural effusion in sarcoidosis may be steroid-resistant. Pleurodesis may have a role in such a scenario.

摘要

背景

结节病是一种病因不明的多系统肉芽肿性疾病。它主要影响肺部,但几乎可以影响任何其他器官。然而,胸膜受累并发展为胸腔积液相对少见。它通常是轻度的,对全身类固醇治疗有反应。在这里,我们报告一例由结节病引起的复发性大量单侧胸腔积液,对全身类固醇治疗耐药。

病例描述

一位 55 岁女性因呼吸困难 2 个月就诊。无其他呼吸道症状。体格检查发现左侧胸腔积液、脾肿大和腹股沟淋巴结肿大。胸部 X 线检查证实了大量胸腔积液。胸腔积液检查显示渗出性胸腔积液伴淋巴细胞为主。全腹部计算机断层扫描显示多个胸、腹和腹股沟淋巴结肿大;此外,还存在左侧胸腔积液和脾脏肿大;脾脏内有不同程度的低密度结节状病变。正电子发射断层扫描-计算机断层扫描显示脾脏和淋巴结摄取增加。腹股沟淋巴结活检显示非坏死性肉芽肿性炎症。由于怀疑恶性肿瘤,进行了左侧胸腔镜检查,壁层胸膜活检显示非特异性炎症,无恶性肿瘤或结核证据。

诊断

根据非坏死性肉芽肿性炎症的发现,结合几个微生物和病理样本均无恶性肿瘤或感染的证据,诊断为结节病。

干预措施

患者接受了多次胸腔积液引流。类固醇治疗未能预防胸腔积液复发。最终进行了左侧胸膜固定术。

结果

随访超过 1 年,患者未再出现胸腔积液复发或出现任何其他症状。

教训

结节病罕见表现为大量胸腔积液,因为这种表现罕见;必须排除大量胸腔积液的其他原因。结节病大量胸腔积液可能对类固醇耐药。在这种情况下,胸膜固定术可能有作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d930/7886481/4e25e49249b6/medi-100-e24027-g001.jpg

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