National Hospital of Sri Lanka, Colombo 08, Sri Lanka.
BMC Infect Dis. 2021 Jun 3;21(1):522. doi: 10.1186/s12879-021-06240-2.
Leptospirosis is a zoonotic spirochetal disease caused by Leptospira interrogans. The clinical presentation ranges from an asymptomatic state to a fatal multiorgan dysfunction. Neurological manifestations including aseptic meningitis, spinal cord and peripheral nerve involvement, cranial neuropathies and cerebellar syndrome are well recognized with varying frequencies among patients with this disease. Posterior reversible encephalopathy syndrome is a very rare occurrence in leptospirosis and only two cases are reported in the medical literature up to now. We report a case of posterior reversible encephalopathy syndrome in a patient with leptospirosis with rhabdomyolysis and acute kidney injury.
A 21 year-old male presented with fever and oliguric acute kidney injury with rhabdomyolysis. A diagnosis of leptospirosis was made and he was being managed according to the standard practice together with regular hemodialysis. The clinical condition was improving gradually. On day 8 of the illness, he developed headache and sudden painless complete bilateral vision loss followed by several brief generalized tonic clonic seizure attacks. Examination was significant for a Glasgow Coma Scale of 14/15, blood pressure of 150/90 mmHg and complete bilateral blindness. The findings of magnetic resonance imaging of the brain were compatible with posterior reversible encephalopathy syndrome. He was managed with blood pressure control and antiepileptics with supportive measures and standard treatment for leptospirosis and made a complete recovery.
Posterior reversible encephalopathy syndrome, though very rare with leptospirosis, should be considered as a differential diagnosis in a patient with new onset visual symptoms and seizures, especially during the immune phase. Optimal supportive care together with careful blood pressure control and seizure management would yield a favourable outcome in this reversible entity.
钩端螺旋体病是一种由问号钩端螺旋体引起的人畜共患螺旋体病。临床表现从无症状状态到多器官功能衰竭不等。神经系统表现包括无菌性脑膜炎、脊髓和周围神经受累、颅神经病变和小脑综合征,在该病患者中频率不一。后部可逆性脑病综合征是钩端螺旋体病中非常罕见的一种,迄今为止仅在医学文献中报告了两例。我们报告了一例钩端螺旋体病合并横纹肌溶解和急性肾损伤的后部可逆性脑病综合征患者。
一名 21 岁男性因发热和少尿性急性肾损伤伴横纹肌溶解症就诊。诊断为钩端螺旋体病,并根据标准治疗方案进行管理,同时定期进行血液透析。临床状况逐渐改善。在疾病的第 8 天,他出现头痛和突发性无痛性双侧视力丧失,随后发生数次短暂全身强直阵挛性发作。检查结果为格拉斯哥昏迷量表评分为 14/15,血压为 150/90mmHg,双侧完全失明。脑部磁共振成像结果符合后部可逆性脑病综合征。他接受了血压控制和抗癫痫药物治疗,并采取了支持措施和标准的钩端螺旋体病治疗,最终完全康复。
后部可逆性脑病综合征虽然在钩端螺旋体病中非常罕见,但在出现新发视觉症状和癫痫发作的患者中,尤其是在免疫期,应考虑作为鉴别诊断。最佳支持治疗,结合仔细的血压控制和癫痫发作管理,对这种可逆转的疾病会产生有利的结果。