PDF(Pubmed)
Abstract：
UNASSIGNED: Scleroderma is a multisystemic disorder characterised by inflammatory and vascular anomalies, and excess fibrosis. Progressive systemic sclerosis (PSS) mainly progresses with skin, joint, lung, heart, and kidney involvement. Involvement of cerebral vessels is rare in both localised scleroderma and PSS. Transient ischemic attack and stroke are rare complications of scleroderma.
UNASSIGNED: We present a 60-year-old stroke patient with localised scleroderma presenting with impaired speech, forgetting words, and occasional temporary memory loss.
UNASSIGNED: In the case we present, no pathology was found in the clinical and laboratory tests performed in terms of ischemic risk factors. Skin findings included contracture, skin biopsy results, and antibody positivity related to scleroderma. Given the current pathogenesis of scleroderma, the patient was suspected of having a stroke.
UNASSIGNED: We present a 60-year-old stroke patient with localised scleroderma presenting with impaired speech, forgetting words, and occasional temporary memory loss.
UNASSIGNED: In the case we present, no pathology was found in the clinical and laboratory tests performed in terms of ischemic risk factors. Skin findings included contracture, skin biopsy results, and antibody positivity related to scleroderma. Given the current pathogenesis of scleroderma, the patient was suspected of having a stroke.
摘要：
■硬皮病是一种以炎症和血管异常为特征的多系统疾病，和过度纤维化。进行性系统性硬化症（PSS）主要随皮肤进展，接头,肺，心,和肾脏受累。在局部硬皮病和PSS中，脑血管的受累很少见。短暂性脑缺血发作和中风是硬皮病的罕见并发症。
■我们介绍了一位60岁的中风患者，患有局限性硬皮病，表现为言语障碍，忘记单词,偶尔会暂时失忆.
■在我们介绍的情况下，在缺血性危险因素方面进行的临床和实验室检查中未发现病理.皮肤表现包括挛缩，皮肤活检结果,与硬皮病相关的抗体阳性。鉴于硬皮病目前的发病机制，病人怀疑中风。
■我们介绍了一位60岁的中风患者，患有局限性硬皮病，表现为言语障碍，忘记单词,偶尔会暂时失忆.
■在我们介绍的情况下，在缺血性危险因素方面进行的临床和实验室检查中未发现病理.皮肤表现包括挛缩，皮肤活检结果,与硬皮病相关的抗体阳性。鉴于硬皮病目前的发病机制，病人怀疑中风。
