Department of Pediatrics, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu City, Mie Prefecture 514-8507, Japan.
BMC Pediatr. 2014 May 31;14:137. doi: 10.1186/1471-2431-14-137.
Idiopathic systemic capillary leak syndrome (ISCLS) is a rare disorder, characterized by episodic life-threatening hypotension, hypoalbuminemia, and hemoconcentration.
A 10-year-old girl presented with abdominal pain, vomiting, diarrhea, fever and developed generalized edema a day after admission. Clinical and laboratory findings were consistent with ISCLS. She received aggressive fluid replacement, methylprednisolone pulse (30 mg/kg/day), high-dose intravenous immunoglobulin (IVIG, 2 g/kg/day) and plasma exchange in acute phase. She received fasciotomy of bilateral lower extremities as she developed complications of compartment syndrome. Since there were two episodes of ISCLS attacks, theophylline and terbutaline were initiated for prevention of attacks and then the remission is currently maintained. Because of high fatality rate in ISCLS, prompt diagnosis and intervention are very important.
We describe here, a rare case of pediatric ISCLS. ISCLS should be considered as a differential diagnosis, when the patient presents with unexplained or sudden hypovolemic shock. Reports on pediatrics ISCLS are very few, and accumulation of similar case reports is needed.
特发性全身性毛细血管渗漏综合征(ISCLS)是一种罕见疾病,其特征为发作性危及生命的低血压、低白蛋白血症和血液浓缩。
一名 10 岁女孩因腹痛、呕吐、腹泻、发热,在入院后一天出现全身水肿。临床和实验室检查结果符合 ISCLS。她在急性期接受了积极的液体替代、甲泼尼龙脉冲(30mg/kg/天)、大剂量静脉注射免疫球蛋白(IVIG,2g/kg/天)和血浆置换。由于出现了四肢间隔综合征的并发症,她接受了双侧下肢的筋膜切开术。由于 ISCLS 发作有两次,因此开始使用茶碱和特布他林预防发作,目前处于缓解状态。由于 ISCLS 死亡率很高,因此及时诊断和干预非常重要。
我们在此描述了一例罕见的儿科 ISCLS 病例。当患者出现不明原因或突然的低血容量性休克时,应考虑 ISCLS 作为鉴别诊断。儿科 ISCLS 的报道非常少,需要积累更多类似的病例报告。