Kumar Nishant, Singh Ranju, Sharma Neha, Jain Aruna
Department of Anaesthesiology, Lady Hardinge Medical College and Smt. SSK Hospital, New Delhi, India.
J Anaesthesiol Clin Pharmacol. 2018 Jan-Mar;34(1):120-122. doi: 10.4103/0970-9185.173351.
Posterior reversible encephalopathy syndrome (PRES) is a clinico-neuroradiological entity, first described in 1996. It is commonly associated with systemic hypertension, intake of immunosuppressant drugs, sepsis and eclampsia and preeclampsia. Headache, alteration in consciousness, visual disturbances and seizures are common manifestations of PRES. Signs of pyramidal tract involvement and motor dysfunction are uncommon clinical findings. However, clinical presentation is not diagnostic. On neuroimaging, lesions are characteristically found in parieto occipital region of the brain due to vasogenic edema. We report two cases of PRES with atypical clinical presentation-one which was suggestive of neurocysticercosis and the other in which agitation and opisthotonic posture were predominant features.
后部可逆性脑病综合征(PRES)是一种临床神经放射学实体,于1996年首次被描述。它通常与系统性高血压、免疫抑制药物的摄入、败血症以及子痫和先兆子痫有关。头痛、意识改变、视觉障碍和癫痫发作是PRES的常见表现。锥体束受累和运动功能障碍的体征是不常见的临床发现。然而,临床表现并无诊断意义。在神经影像学上,由于血管源性水肿,特征性病变见于大脑的枕顶叶区域。我们报告两例具有非典型临床表现的PRES病例——一例提示神经囊尾蚴病,另一例以躁动和角弓反张姿势为主要特征。