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"Human immunodeficiency virus"

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"Human immunodeficiency virus"

Chronic Inflammatory Demyelinating PolyneuropathyAssociated with HIV-Infection
So-Young Huh, Bo-Young Ahn, Se-Jin Oh, Yeong-Eun Park, Dae-Seong Kim
J Korean Soc Clin Neurophysiol 2011;13(2):97-100.
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired immune-mediated polyneuropathy. Corticosteroids,intravenous immunoglobulin (IVIG) and plasmapheresis have been reported to be effective treatment. Rarely, CIDP can occurin the patients with HIV infection. The clinical features and electrophysiological findings of CIDP are known to be similarin patients with and without HIV infection. We report a 30-year-old male with HIV infection associated CIDP who improvedafter the administration of intravenous immunoglobulin and long term oral prednisone.
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Peripheral Neuropathy Associated with Human Immunodeficiency Virus Infection
Min Hwan Lee, Young-Min Lim, So Young Pyun, Jimin Kim, Kwang-kuk Kim
J Korean Soc Clin Neurophysiol 2012;14(1):29-35.
Background
Peripheral neuropathy is the most frequent neurological complication in human immunodeficiency virus (HIV)infection, related with diverse etiologies including inflammation, opportunistic infection and side effects of medications. Thepurpose of the present study was to evaluate characteristics of HIV associated neuropathy according to the stage of HIVinfection. Methods: In reviewing the medical records of HIV patients who underwent electrodiagnostic studies between 1997and 2011, total 11 patients (all males; median age, 47 years; range, 28-71 years) with comorbid neuropathy were enrolled. Stageof HIV infection was categorized according to the Centers for Disease Control and Prevention (CDC) criteria. Classificationof peripheral neuropathy was based on clinical and electrophysiological features. Results: Distal symmetric polyneuropathywas observed in 8 patients (72.7%), inflammatory demyelinating polyneuropathy in 2 patients (18.1%), and polyradiculopathyin 1 patient (9.1%). Median CD4+ T cell count was 123/mm3 (range, 8-540/mm3) and 7 patients (60%) had the mostadvanced HIV disease stage (CDC-C3). There was no neuropathy caused by CMV infection. Conclusions: Distal symmetricpolyneuropathy was the most common type of neuropathy in HIV infection, but various forms of neuropathy such asinflammatory demyelinating polyneuropathy and polyradiculopathy were also present. HIV associated neuropathy is morefrequently associated with advancing immunosuppression, although it can occur in all stages of HIV infection.
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