小儿肉芽肿性多血管炎患者中假性脑瘤的罕见表现

Rare Presentation of Pseudotumor Cerebri in a Pediatric Patient With Granulomatosis With Polyangiitis.

作者信息

Sioufi Henry J, Makvandi Shayan, Masoud Rana, Wu Xiaoyan, Abdul-Aziz Rabheh

机构信息

Pediatrics, Oishei Children's Hospital/University at Buffalo, Buffalo, USA.

Pediatric Nephrology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, USA.

出版信息

Cureus. 2020 Nov 19;12(11):e11567. doi: 10.7759/cureus.11567.

DOI:10.7759/cureus.11567

PMID:33364094

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7749803/

Abstract

We present a case of an 11-year-old female with granulomatosis with polyangiitis (GPA) diagnosed one year prior to presentation, stage III chronic kidney disease (CKD), hypertension (HTN), obstructive sleep apnea (OSA), and chronic anemia who presented with headache, nausea, vomiting, and diplopia and was found to have idiopathic intracranial hypertension (IIH). IIH was reported in adults with GPA and for our knowledge has not been yet reported in pediatric cases of GPA.

摘要

我们报告一例11岁女性，患有肉芽肿性多血管炎（GPA），在就诊前一年确诊，伴有III期慢性肾脏病（CKD）、高血压（HTN）、阻塞性睡眠呼吸暂停（OSA）和慢性贫血，此次因头痛、恶心、呕吐和复视而就诊，被发现患有特发性颅内高压（IIH）。特发性颅内高压在成年GPA患者中已有报道，但据我们所知，在儿童GPA病例中尚未见报道。