Ma Fan, Zhou Kaiyu, Hua Yimin, Liu Xiaoliang, Duan Hongyu, Li Yifei, Wang Chuan
Department of Pediatric Cardiology, West China Second University Hospital, Sichuan University.
The Cardiac Development and Early Intervention Unit, West China Institute of Women and Children's Health, West China Second University Hospital, Sichuan University.
Medicine (Baltimore). 2018 Oct;97(41):e12349. doi: 10.1097/MD.0000000000012349.
Chronic thromboembolic pulmonary hypertension (CTEPH) is rare in children and determining the underlying etiologies is essential for treatment. Venous thromboembolism, a well-known complication in nephrotic syndrome (NS), always occurrs during the treatment in course of the disease. However, CTEPH as the first manifestation of NS has not been reported till now.
A 12-year-old boy initially complained of hemoptysis, cough and shortness of breath with exertion, any symptoms regarding NS such as edema were not presented. Due to the identification of P2 enhancement, liver enlargement (2 cm below the rib) and jugular vein distension, pulmonary hypertension (PH) was firstly suspected and ultimately confirmed by detection of enlargement of right atrium (RA) and right ventricle (RV) enlargement (RA = 45mm, RV = 30mm), mild tricuspid valve regurgitation (TR) and elevation of pulmonary arterial pressure (63 mmHg) on echocardiogram. In order to search the underlying causes of PH, series of targeted laboratory evaluation and imaging were conducted, and pulmonary arterial embolism (PE) in inferior lobes of double lungs was found on chest contrast-enhanced computed tomography.
NS was unexpectedly discovered by detection of lower serum albumin level (24.4 g/L), severe proteinuria (+++, 4.62 g/24 h) when we were searching for the predisposing factors causing thromboembolism.
After treatment of NS, the symptom regarding shortness of breath with exertion gradually became less apparent and was relieved one month later. Proteinuria and microscopic hematuria also disappeared. Encouragingly, RA and RV dilation, and the pulmonary arterial pressure almost returned to a normal range half a year later, with alleviation of MR.
CTEPH can occur rarely in children and NS is an important predisposing factor. PE could be the first manifestation of NS. When pediatricians encounter children with PE or CTEPH, NS as the underlying etiology should be considered. Except for renal venous thrombosis, the possibility of PE needs to be paid more attention in children with NS.
慢性血栓栓塞性肺动脉高压(CTEPH)在儿童中较为罕见,确定其潜在病因对治疗至关重要。静脉血栓栓塞是肾病综合征(NS)的一种常见并发症,通常在疾病治疗过程中发生。然而,CTEPH作为NS的首发表现至今尚未见报道。
一名12岁男孩最初主诉咯血、咳嗽及活动后气短,未出现任何与NS相关的症状,如水肿。由于发现P2亢进、肝脏肿大(肋下2cm)及颈静脉怒张,首先怀疑为肺动脉高压(PH),最终经超声心动图检查发现右心房(RA)扩大及右心室(RV)扩大(RA = 45mm,RV = 30mm)、轻度三尖瓣反流(TR)及肺动脉压升高(63mmHg)得以确诊。为寻找PH的潜在病因,进行了一系列针对性实验室检查及影像学检查,胸部增强CT发现双肺下叶肺动脉栓塞(PE)。
在寻找导致血栓栓塞的易感因素时,意外发现血清白蛋白水平降低(24.4g/L)、重度蛋白尿(+++,4.62g/24h),从而确诊为NS。
NS治疗后,活动后气短症状逐渐减轻,1个月后缓解。蛋白尿及镜下血尿也消失。令人鼓舞的是,半年后RA及RV扩张、肺动脉压几乎恢复正常范围,MR减轻。
CTEPH在儿童中罕见,NS是重要的易感因素。PE可能是NS的首发表现。儿科医生遇到患有PE或CTEPH的儿童时,应考虑NS作为潜在病因。除肾静脉血栓形成外,NS患儿中PE的可能性更应引起重视。