Rao Prasanna K S, Sheth Keyur A, Nadig Raghunandan, Patil Mallikarjun, Channagiri Adarsh K
St. John's Medical College, Bangalore, Karnataka, India.
J Clin Exp Hepatol. 2012 Dec;2(4):393-5. doi: 10.1016/j.jceh.2012.10.005. Epub 2012 Oct 22.
Portosystemic myelopathy is an unusual complication in patients with chronic liver disease with hepatic encephalopathy and portosystemic shunts. Here we present a case of 35-year-old male patient who presented to us with difficulty in walking and progressive stiffness in both lower limbs for two months. He had undergone splenectomy with distal splenorenal shunt 20 years back. On physical examination, he had spasticity in both lower limbs of grade 3, with minimal pyramidal weakness in lower limbs, brisk knee and ankle jerks. The plantar response was extensor. Upper limb examination was normal. On investigations, he had hypoalbuminemia, hyperbilirubinemia, increased plasma ammonia levels. Contrast enhanced CT scan abdomen revealed dilated splenorenal shunt and MRI spine showed no spinal cord compression. Electromyoneurogram was also normal. Spastic paraparesis due to portosystemic shunts was diagnosed. Liver transplantation can reverse the myelopathy only in earlier stages, hence early and accurate diagnosis is important.
门体性脊髓病是慢性肝病合并肝性脑病和门体分流患者的一种罕见并发症。在此,我们报告一例35岁男性患者,该患者因行走困难和双下肢进行性僵硬两个月前来就诊。他20年前接受了脾切除术及远端脾肾分流术。体格检查时,他双下肢痉挛程度为3级,下肢有轻微锥体束征性肌无力,膝腱和跟腱反射亢进。跖反射为伸性。上肢检查正常。检查发现,他有低白蛋白血症、高胆红素血症、血浆氨水平升高。腹部增强CT扫描显示脾肾分流扩张,脊柱MRI显示无脊髓受压。肌电图也正常。诊断为门体分流所致痉挛性截瘫。肝移植仅在早期阶段可逆转脊髓病,因此早期准确诊断很重要。