Posterior reversible encephalopathy syndrome associated with Henoch Schonlein Purpura in a pediatric patient

被引:2
作者
Fikse, Derek J. [1 ]
Grenz, Phillip M. [1 ]
Wheatley, Scott M. [2 ]
Fugok, Kimberly L. [1 ]
机构
[1] Univ S Florida, Lehigh Valley Reilly Childrens Hosp Lehigh Valley, Dept Emergency & Hosp Med,Morsani Coll Med, Div Pediat Emergency Med,Lehigh Valley Hlth Netwo, Cedar Crest Blvd & 1-78, Allentown, PA 18103 USA
[2] Univ S Florida, Lehigh Valley Reilly Childrens Hosp Lehigh Valley, Morsani Coll Med, Lehigh Valley Hlth Network,Dept Pediat, Lehigh Valley Campus,Cedar Crest Blvd & 1-78, Allentown, PA 18103 USA
关键词
HSP; IgA Vasculitis; PRES; Pediatrics;
D O I
10.1016/j.ajem.2020.10.024
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Henoch Schonlein Purpura is a rare hypersensitivity vasculitis that is commonly associated with pediatric patients. It typically presents with purpuric rash to the lower extremities, abdominal pain and microscopic hematuria; however, it may also be associated with intussusception, glomerulonephritis and hypertension. Posterior Reversible Encephalopathy Syndrome is a poorly understood, rare condition associated with cerebral edema and segmental vasoconstriction. Typically characterized by headaches, seizures, and visual changes, which is presumed to be associated with rapid increases in blood pressure. We present the case of a 6-year-old female who developed Posterior Reversible Encephalopathy Syndrome as a complication from Henoch Schonlein Purpura. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:291.e5 / 291.e7
页数:3
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