Neurological PRESentations in Sickle Cell Patients Are Not Always Stroke: A Review of Posterior Reversible Encephalopathy Syndrome in Sickle Cell Disease

被引:27
作者
Solh, Ziad [1 ]
Taccone, Michael S. [2 ]
Marin, Samantha [3 ]
Athale, Uma [1 ]
Breakey, Vicky R. [1 ]
机构
[1] McMaster Univ, McMaster Childrens Hosp, Div Pediat Hematol & Oncol, Dept Pediat, HSC 3N27a-1280 Main St W, Hamilton, ON L8S 4K1, Canada
[2] Univ Ottawa, Dept Surg, Ottawa Hosp, Div Neurosurg, Ottawa, ON, Canada
[3] Univ Manitoba, Hlth Sci Ctr, Dept Pediat, Div Pediat Neurol, Winnipeg, MB, Canada
关键词
posterior reversible encephalopathy syndrome; sickle cell disease; stroke; transfusion; HEMATOPOIETIC STEM-CELL; CEREBRAL VASOCONSTRICTION SYNDROME; ACUTE CHEST SYNDROME; LEUKOENCEPHALOPATHY SYNDROME; BLOOD-TRANSFUSION; CHILDREN; TRANSPLANTATION; ANEMIA; PRES; PATHOPHYSIOLOGY;
D O I
10.1002/pbc.25932
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acute neurological changes in sickle cell disease (SCD) patients often raise the suspicion for stroke. Posterior reversible encephalopathy syndrome (PRES) can mimic stroke in its clinical presentation. We aimed to (i) review the PRES literature in SCD patients including clinical presentation, risk factors, pathophysiology, and management and (ii) elucidate the distinction between PRES and stroke in SCD. The exact pathophysiology of PRES in SCD remains elusive but is likely multifactorial and related to sickling, ischemia, and chronic anemia predisposing to vasogenic edema. PRES and stroke in SCD are distinguishable conditions. Our review may help elucidate a clinical approach to this distinction.
引用
收藏
页码:983 / 989
页数:7
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