Banakar Basavaraj F, Pujar Guruprasad S, Bhargava Amita, Khichar Shubhkaran
Department of Neurology, Dr. S N Medical College, Jodhpur, Rajasthan, India.
J Neurosci Rural Pract. 2014 Jan;5(1):63-5. doi: 10.4103/0976-3147.127877.
Posterior reversible encephalopathy syndrome (PRES) is a clinicoradiologic entity commonly associated with eclampsia, septicemia, chemotherapeutic drugs etc. Concurrent occurrence of Guillain-Barre syndrome (GBS) with PRES is a rare entity. Dysautonomia is a proposed mechanism for such occurrence. Here we present a non-diabetic, non-hypertensive 63-year-old male patient, who came with acute onset flaccid quadriparesis, developing generalized seizures, altered sensorium and raised blood pressure on fifth day of illness. Magnetic resonance imaging (MRI) of brain showed altered signal intensities involving the parieto-occipital areas suggestive of posterior reversible encephalopathy. Cerebrospinal fluid analysis showed albuminocytological dissociation, nerve conduction studies revealed demyelinating type of polyneuropathy. The patient was treated with antihypertensives and antiepileptics. After resolution of the encephalopathy, intravenous immunoglobulin (IVIg) was given. The patient recovered gradually over few months. Our case concludes GBS as independent risk factor, for PRES may be secondary to dysautonomia and physicians should be aware of such rare coexistence so that early treatment can be done to reduce the mortality and morbidity.
后部可逆性脑病综合征(PRES)是一种临床放射学实体,通常与子痫、败血症、化疗药物等相关。格林-巴利综合征(GBS)与PRES同时出现是一种罕见情况。自主神经功能障碍是这种情况发生的一种推测机制。在此,我们报告一名63岁非糖尿病、非高血压男性患者,他因急性起病的弛缓性四肢瘫前来就诊,在患病第5天出现全身性癫痫发作、意识改变和血压升高。脑部磁共振成像(MRI)显示顶枕叶区域信号强度改变,提示后部可逆性脑病。脑脊液分析显示蛋白细胞分离,神经传导研究显示脱髓鞘型多发性神经病。患者接受了抗高血压药和抗癫痫药治疗。脑病缓解后,给予静脉注射免疫球蛋白(IVIg)。患者在几个月内逐渐康复。我们的病例表明GBS是一个独立的危险因素,PRES可能继发于自主神经功能障碍,医生应意识到这种罕见的共存情况,以便能进行早期治疗以降低死亡率和发病率。