Neurological manifestations of Degos disease

D. I. Abzalova, M. Sinkin, O. V. Kisyel, A. Grin
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Abstract

Degos disease is a rare disease that manifests itself as multifocal vasculopathy, the consequence of which is the defeat of many systems, including the nervous system. This disease is difficult to diagnose, today it does not have a standardized approach to treatment, and it is deadly.In the presented clinical case, the course of BD is described in a 66-year-old patient, whose debut of the disease was a lesion of the skin. The cause of hospitalization of the patient was the defeat of the central nervous system. During the additional examination, the patient was diagnosed with ischemic stroke in the basin of the left middle cerebral artery, posterior cerebral artery, right middle cerebral artery of another established etiology according to TOAST, aseptic leptomeningitis, pachymeningitis. The course of the disease was complicated by damage to the gastrointestinal tract, the cardiovascular system, as well as the addition of a coronavirus infection, which led to death.
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Degos病的神经系统表现
Degos病是一种罕见的疾病,表现为多灶性血管病,其后果是包括神经系统在内的许多系统的衰竭。这种疾病很难诊断,如今没有标准化的治疗方法,而且是致命的。在本临床病例中,BD的病程描述为一名66岁的患者,其首次发病是皮肤损伤。病人住院的原因是中枢神经系统衰竭。在附加检查中,根据TOAST,患者被诊断为另一种确定病因的左侧大脑中动脉、大脑后动脉、右侧大脑中动脉盆地缺血性中风、无菌性钩端脑膜炎、厚壁炎。胃肠道、心血管系统受损,加上冠状病毒感染,导致死亡,使疾病的进程变得复杂。
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来源期刊
Russian Neurological Journal
Russian Neurological Journal Medicine-Neurology (clinical)
CiteScore
0.40
自引率
0.00%
发文量
49
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