Kadwa Razia A, Sankhyan Naveen, Ahuja Chirag K, Singhi Pratibha
Department of Pediatric Neurology, Superspeciality Pediatric Hospital and Post Graduate Teaching Institute, Uttar Pradesh, India.
Department of Pediatrics, Advanced Pediatric Center, Division of Pediatric Neurology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
J Pediatr Neurosci. 2019 Jan-Mar;14(1):36-37. doi: 10.4103/jpn.JPN_12_18.
We describe a 10 year old boy who presented with acute onset rapidly progressing encephalopathy. MRI revealed bilateral insular cortex and basifrontal involvement suggesting Herpes encephalitis.He was treated with acyclovir and his symptoms improved. Six months after the first hospitalization he reported back with two episodes of partial seizures. He was started on Valproate. A week after starting valproate he was readmitted with hyperammonemic encephalpathy, on further investigations Citrullinemia Type 1 was diagnosed. This case highlights a metabolic disorder which radiologically mimics herpes encephalitis. The management of the disorder differs remarkably from herpes encephalitis and hence its recognition and suspicion based on radiology is critical.
我们描述了一名10岁男孩,他出现急性起病且迅速进展的脑病。磁共振成像(MRI)显示双侧岛叶皮质和基底额叶受累,提示为疱疹性脑炎。他接受了阿昔洛韦治疗,症状有所改善。首次住院6个月后,他因两次部分性癫痫发作前来复诊。他开始服用丙戊酸盐。开始服用丙戊酸盐一周后,他因高氨血症性脑病再次入院,进一步检查后诊断为1型瓜氨酸血症。该病例突出了一种在放射学上酷似疱疹性脑炎的代谢紊乱疾病。该疾病的治疗与疱疹性脑炎明显不同,因此基于放射学进行识别和怀疑至关重要。