Anand Sucharita, Das Animesh, Choudhury Surjyaprakash Shivnarayan
Department of Neurology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
BMJ Case Rep. 2019 Jan 7;12(1):e226259. doi: 10.1136/bcr-2018-226259.
A 26-year-old patient of limited cutaneous sclerosis presented to us with insidious-onset posterior fossa symptoms of headache, vomiting, vertigo and gait imbalance, progressing over a period of 3 weeks. A diagnosis of chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids was made by combining the clinical features with radiological evidence showing punctate infiltration of the pons, brainstem and cerebellum. Relevant differentials in the form of neurosarcoid, infections, central nervous system (CNS) lymphoma and Neuro-Behcet's disease were ruled out by history and investigations. The patient responded dramatically to steroid therapy, and had no neurological deficits after 18 months of follow-up. This case highlights the rare association of a not-so-common immunological disease with a rare neurological disease.
一名26岁的局限性皮肤硬化症患者前来就诊,隐匿起病,出现后颅窝症状,如头痛、呕吐、眩晕和步态失衡,持续3周。结合临床特征和影像学证据(显示脑桥、脑干和小脑有斑点状浸润),诊断为对类固醇有反应的慢性淋巴细胞性炎症伴脑桥血管周围强化。通过病史和检查排除了神经结节病、感染、中枢神经系统淋巴瘤和神经白塞病等相关鉴别诊断。患者对类固醇治疗反应显著,随访18个月后无神经功能缺损。该病例突出了一种不太常见的免疫性疾病与一种罕见的神经系统疾病之间的罕见关联。