Corbally Conal M, Breckenridge Andrew, Jampana Ravi
Department of Radiology, Institute of Neurological Sciences, Glasgow, UK.
Department of Neurology, Institute of Neurological Sciences, Glasgow, UK.
BJR Case Rep. 2016 Nov 2;2(4):20150203. doi: 10.1259/bjrcr.20150203. eCollection 2016.
We present the case of a 58-year-old female presenting with acute onset headache and decrease in left-sided facial sensation. The patient's background included diabetes Type 2, hypertension, migraine, anxiety with depression and scleroderma in her childhood. Imaging revealed foci of right frontal calcification and confluent white matter changes, reported as sequelae of a previous ischaemic episode. Following a second presentation with the same symptoms, further imaging showed a linear soft tissue scar overlying these changes, which suggested a diagnosis of linear scleroderma (en coup de sabre). On questioning, it was found that this had developed during the patient's late teens but had not progressed since that time. Coup de sabre type linear scleroderma is often associated with intracranial imaging findings, even in the absence of symptoms. The pathogenesis of neurological symptoms is poorly understood but does seem to respond to immunosuppression.
我们报告了一例58岁女性患者,其出现急性头痛并伴有左侧面部感觉减退。患者既往病史包括2型糖尿病、高血压、偏头痛、焦虑伴抑郁以及童年时期患硬皮病。影像学检查显示右额叶钙化灶和融合性白质改变,报告为既往缺血性发作的后遗症。在第二次出现相同症状后,进一步影像学检查显示这些改变上方有一条线性软组织瘢痕,提示诊断为线性硬皮病(剑伤型)。经询问,发现这是在患者青少年晚期出现的,但此后未再进展。剑伤型线性硬皮病即使在没有症状的情况下也常与颅内影像学表现相关。神经症状的发病机制尚不清楚,但似乎对免疫抑制有反应。