A rare angiopathy with lesions of the skin and central nervous system: Sneddon syndrome and disease
نویسندگان
چکیده
Sneddon syndrome is a rare, progressive disease that affects relatively young people, mainly female, and manifests itself in two main symptoms: livedo reticularis recurrent cerebral infarctions. First described 1965 by the English dermatologist Ian Bruce Sneddon, named his honor unites heterogeneous group of diseases with different pathogenesis similar clinical manifestations. Skin manifestations form reticular are benign, cerebrovascular reduced to repeated infarctions, dementia can lead death patients. The literature review describes basic concepts etiology, primary secondary forms syndrome, proposes concept Sneddon’s describe syndrome. article contains photographs patients from practice authors article. also methods diagnosis differential recommended treatment, which based on elimination additional risk factors for vascular damage thrombosis, blood pressure control, lipid carbohydrate metabolism, as well appointment anticoagulant disaggregant therapy. use anti-inflammatory or immunosuppressive therapy remains controversial. goal treatment prevention organic brain neuropsychiatric complications. Unfortunately, prognosis poor development impaired memory, concentration, visual-spatial skills. In exceptional cases, progression death.
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ژورنال
عنوان ژورنال: Juvenis scientia
سال: 2022
ISSN: ['2414-3790', '2414-3782']
DOI: https://doi.org/10.32415/jscientia_2022_8_6_15-29