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小儿遗传性血管性水肿作为手和前臂急性骨筋膜室综合征的病因:一例报告

Pediatric Hereditary Angioedema as a Cause of Acute Compartment Syndrome of the Hand and Forearm: A Case Report.

作者信息

Venditto Chelsea, Jager Zachary, LoGiudice John, Matloub Hani

机构信息

1 Medical College of Wisconsin, Milwaukee, USA.

2 Zablocki VA Medical Center, Milwaukee, WI, USA.

出版信息

Hand (N Y). 2017 May;12(3):NP46-NP50. doi: 10.1177/1558944716668830. Epub 2016 Oct 7.

Abstract

BACKGROUND

Compartment syndrome of the upper extremity is a surgical emergency that, when left untreated, can have dire consequences. Its causes are numerous, one of which is the uncommon entity hereditary angioedema, an autosomal dominant disease resulting in edema in a variety of potential locations, including the extremities. This is only the second time hereditary angioedema has been mentioned in the literature as a cause of compartment syndrome.

METHODS

We present a case of hereditary angioedema leading to hand and forearm compartment syndrome in a 13-year-old pediatric patient. Diagnosis of hereditary angioedema was made by our Rheumatology colleagues with physical exam and a thorough history, and confirmed by laboratory studies.

RESULTS

Our patient presented with compartment syndrome of the hand and forearm and underwent hand and volar forearm fasciotomies. She was subsequently worked up for hereditary angioedema with laboratory results confirming the diagnosis. She was discharged after a 5-day hospitalization with prophylactic C1-inhibitor therapy.

CONCLUSIONS

Hereditary angioedema is a rare but known cause of compartment syndrome of the upper extremity, and must be considered when patients present with compartment syndrome of unknown etiology. This disease can be diagnosed by laboratory studies and symptoms can be controlled with medical therapy.

摘要

背景

上肢骨筋膜室综合征是一种外科急症,若不治疗会产生严重后果。其病因众多,其中之一是罕见的遗传性血管性水肿,这是一种常染色体显性疾病,可导致包括四肢在内的多种潜在部位出现水肿。这是文献中第二次提及遗传性血管性水肿作为骨筋膜室综合征的病因。

方法

我们报告一例13岁儿科患者因遗传性血管性水肿导致手部和前臂骨筋膜室综合征的病例。遗传性血管性水肿的诊断由我们的风湿病学同事通过体格检查和详细病史做出,并经实验室检查证实。

结果

我们的患者出现手部和前臂骨筋膜室综合征,并接受了手部和掌侧前臂筋膜切开术。随后对她进行了遗传性血管性水肿检查,实验室结果证实了诊断。她在住院5天后接受预防性C1抑制剂治疗后出院。

结论

遗传性血管性水肿是上肢骨筋膜室综合征一种罕见但已知的病因,当患者出现病因不明的骨筋膜室综合征时必须予以考虑。这种疾病可通过实验室检查诊断,症状可用药物治疗控制。

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