کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3391141 | 1221003 | 2009 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
LeucoencefalopatÃa multifocal progresiva: desde el origen a 2008
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کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
ایمونولوژی، آلرژی و روماتولوژی
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چکیده انگلیسی
The term progressive multifocal leukoencephalopathy (PML) denotes a demyelinating neurological disease caused by oligodendrocyte destruction produced by reactivation of human polyomavirus JC, usually acquired in childhood. The advent of acquired immunodeficiency syndrome (AIDS) has contributed to the marked increase in the frequency of this disease and to incomplete discovery of the complex and close molecular relations between JC and human immunodeficiency virus (HIV). Clinical manifestations are nonspecific and are typical of any demyelinating disease, although PML is more aggressive and has a poor prognosis. Definitive diagnosis is based on histological analysis, but neuroimaging and polymerase chain reaction for JC virus in cerebrospinal fluid can also be used. There is no curative therapy. Autoimmune diseases and, recently, iatrogenic damage by immunosuppressors and monoclonal antibodies, are other causes of this disease.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Seminarios de la Fundación Española de ReumatologÃa - Volume 10, Issue 3, JulyâSeptember 2009, Pages 91-99
Journal: Seminarios de la Fundación Española de ReumatologÃa - Volume 10, Issue 3, JulyâSeptember 2009, Pages 91-99
نویسندگان
MarÃa Begoña Gómez González, MarÃa Teresa Pérez Gracia, Manuel Antonio RodrÃguez Iglesias, José Antonio Girón González, MÃriam Sillero Sánchez, MarÃa de la Cruz Ballester DÃaz, Juan José Asencio Marchante,