Neurological Complications in Sickle Cell Disease

H. Al-Jafar, R. Alroughani, T. Abdullah, Fatma Al-Qallaf
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引用次数: 11

Abstract

Sickle cell disease is a common inherited blood disorder that affects red blood cells. It is a hemoglobinopathy characterized by hemoglobin polymerization, erythrocyte stiffening, and subsequent vaso-occlusions. These changes can lead to microcirculation obstructions, tissue ischemia, infarction and acute stroke. In addition, chronic cerebral ischemia and cerebral vascular anomalies are considered among the most disabling problems in sickle cell disease. Neurological complications of sickle cell disease include, Ischaemic Stroke, hemorrhagic stroke, transient ischemic attack, silent cerebral infarction, headache, Moyamoya disease, neuropathic pain, and neurocognitive impairment. Early diagnosis and proper management of sickle cell disease neurological complications require specialised hematological and neurological experties. The newly used medications under ongoing research foster the hope to overcome this devastating disease and its complications.
镰状细胞病的神经系统并发症
镰状细胞病是一种常见的遗传性血液疾病,影响红细胞。这是一种以血红蛋白聚合、红细胞硬化和随后的血管闭塞为特征的血红蛋白病。这些变化可导致微循环阻塞、组织缺血、梗死和急性卒中。此外,慢性脑缺血和脑血管异常被认为是镰状细胞病最致残的问题。镰状细胞病的神经系统并发症包括缺血性卒中、出血性卒中、短暂性脑缺血发作、无症状性脑梗死、头痛、烟雾病、神经性疼痛和神经认知障碍。镰状细胞病神经并发症的早期诊断和适当管理需要专门的血液学和神经学专业知识。正在进行的研究中使用的新药物为克服这种毁灭性疾病及其并发症带来了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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