Zhang Xuan, Wu Wenbin
Medicine (Baltimore). 2018 Dec;97(51):e13708. doi: 10.1097/MD.0000000000013708.
Systemic lupus erythematosus (SLE) is a connective tissue disease that has many clinical manifestations. However, cardiac tamponade has been rarely reported especially as an initial presenting feature of systemic lupus erythematosus. Herein, we describe a case of cardiac tamponade as the first presentation of systemic lupus erythematosus in a male and presented the course of diagnosis and treatment of this patient.
A 32-year-old male patient developed a rapid progression of pericardial effusion and he was almost healthy in the past. Vital signs were significantly marked by high fever, tachycardia, and accelerated breathing rate of 37 times per minute. The ANA titer was 1:320 and anti-dsDNA was positive during his hospitalization. The complement levels were decreased but the ESR and the CRP level were increased obviously. Soon after, he appeared anemic and thrombocytopenic.
The diagnosis of SLE was made based on the clinical and biochemical findings according to 2012 SLICC SLE Criteria.
The interventions included use CT-guided pericardial puncture to relieve symptoms in time; utilize high-dose glucocorticoids and immunosuppressants to therapy SLE; closely monitor the vital signs, blood routine, blood biochemical indicators, and volume of pericardial effusion.
After 2 months, the symptoms were disappeared almost completely and TTE showed his pericardial effusion had decreased significantly.
We should also keep SLE in mind when assessing male patients with pericardial effusions. Early examinations of sero-immunological markers and closely monitoring the performances are important for the diagnosis of the disease. Early pericardial puncture can quickly relieve symptoms and improve prognosis.
系统性红斑狼疮(SLE)是一种具有多种临床表现的结缔组织病。然而,心包填塞很少被报道,尤其是作为系统性红斑狼疮的首发特征。在此,我们描述了一例男性患者以心包填塞为系统性红斑狼疮的首次表现,并呈现了该患者的诊断和治疗过程。
一名32岁男性患者心包积液迅速进展,他既往几乎健康。生命体征显著表现为高热、心动过速以及呼吸频率加快至每分钟37次。住院期间抗核抗体滴度为1:320,抗双链DNA阳性。补体水平降低,但血沉和C反应蛋白水平明显升高。不久后,他出现贫血和血小板减少。
根据2012年SLICC系统性红斑狼疮标准,基于临床和生化检查结果做出系统性红斑狼疮的诊断。
干预措施包括及时使用CT引导下心包穿刺以缓解症状;使用大剂量糖皮质激素和免疫抑制剂治疗系统性红斑狼疮;密切监测生命体征、血常规、血液生化指标以及心包积液量。
2个月后,症状几乎完全消失,经胸超声心动图显示其心包积液显著减少。
在评估有心包积液的男性患者时,我们也应考虑到系统性红斑狼疮。早期进行血清免疫标志物检查并密切监测病情表现对疾病诊断很重要。早期心包穿刺可迅速缓解症状并改善预后。