کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8689811 | 1581068 | 2018 | 16 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Inclusion body myositis and human immunodeficiency virus type 1: A new case report and literature review
ترجمه فارسی عنوان
میوزیت درگیر شدن با بیماری و ویروس نقص ایمنی بدن نوع 1: گزارش مورد جدید و بررسی ادبیات
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کلمات کلیدی
میوزیت بدنی ویروس نقص ایمنی بدن نوع 1، پیری زودرس،
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب تکاملی
چکیده انگلیسی
Prevalence of muscle disease in human immunodeficiency virus (HIV) infection is less than 1% of patients with acquired immune deficiency syndrome. Sporadic inclusion body myositis (IBM) is observed in a few cases of patients infected by retroviruses such as HIV-1. A Caucasian man was diagnosed with HIV when he was 30 years old. The viral load was undetectable and CD4 cell count was 600/mm3 when the diagnosis of inclusion body myositis was confirmed. Histological findings were typical of IBM. The treatment consisted of immunoglobulin therapy for three years without effect. Twenty-two patients were found in the English and French literature. They are younger than those who suffer from IBM without HIV (median ageâ=â47, range: 30 to 59), and they are mostly men with considerable serum creatine kinase (CK) elevation (median CK levelâ=â1322âIU/L, range: 465 to 10270), most of them were treated with Zidovudine.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuromuscular Disorders - Volume 28, Issue 4, April 2018, Pages 334-338
Journal: Neuromuscular Disorders - Volume 28, Issue 4, April 2018, Pages 334-338
نویسندگان
Priscille Couture, Edoardo Malfatti, Geneviève Morau, Alexis Mathian, Fleur Cohen-Aubart, Hubert Nielly, Zahir Amoura, Patrick Cherin,