Karoui Mehdi, Baklouti Emna, Ben Mohamed Dina, Riahi Hend, Chelli-Bouaziz Mouna
Razi Hospital Psychiatry G oranges street Manouba Tunisia.
Neurology La Rabta Tunisia Tunis Institut National de Neurologie Mongi-Ben Hamida Tunis Tunisia.
Clin Case Rep. 2023 Oct 4;11(10):e8013. doi: 10.1002/ccr3.8013. eCollection 2023 Oct.
The diagnosis of Sneddon Syndrome should be considered in adults with young-onset dementia accompanied by neuropsychiatric signs and livedo racemosa. Magnetic resonance imaging and cerebral angiography are essential. A cutaneous biopsy may help in the diagnosis.
Sneddon syndrome (SS) is a clinical entity corresponding to a noninflammatory thrombotic vasculopathy that typically includes livedo racemosa and cerebrovascular ischemia. Psychiatric symptoms with cognitive impairment often occur but are rarely the inaugural symptoms. We present a case of secondary SS in a 45-year-old man in whom dementia and psychosis revealed the disease.
对于患有早发性痴呆并伴有神经精神症状和网状青斑的成年人,应考虑斯内登综合征的诊断。磁共振成像和脑血管造影至关重要。皮肤活检可能有助于诊断。
斯内登综合征(SS)是一种与非炎性血栓性血管病相对应的临床实体,通常包括网状青斑和脑血管缺血。常出现伴有认知障碍的精神症状,但很少作为首发症状。我们报告一例45岁男性继发性SS病例,该患者的痴呆和精神病症状揭示了此病。