Abstract:ABSTRACT. Background. Peripheral neuropathy in children with human immunodeficiency virus (HIV) infection has not been systematically studied.Objectives. To describe the symptoms and signs of peripheral neuropathy in HIV-infected children and to determine their frequency.Methods. A cross-sectional study was conducted on a convenience sample from a cohort of children older than 5 years of age at the pediatric HIV outpatient clinic of the Federal University of Rio de Janeiro. Those patients were interviewed and … Show more
“…Damage to small-diameter axons in peripheral nerves and DRG neurons are the hallmarks of HIV-1 associated DSP (Bradley et al, 1998;Araujo et al, 2000). Nonetheless, little is known about the contribution of infiltrating lymphocytes in terms of neuronal injury in DRGs of HIV-infected patients with DSP.…”
“…Damage to small-diameter axons in peripheral nerves and DRG neurons are the hallmarks of HIV-1 associated DSP (Bradley et al, 1998;Araujo et al, 2000). Nonetheless, little is known about the contribution of infiltrating lymphocytes in terms of neuronal injury in DRGs of HIV-infected patients with DSP.…”
“…11,12 The higher prevalence reported in the Brazilian study may be partially explained by their case definition; if children with both symptoms and electromography evidence of DSPN in the lower limbs are included, then only 18% (7 of 39) met criteria for DSPN. Our study used diagnostic criteria recommended by AAN and AAEM experts, and included a combination of symptoms, neurologic examination, and electrophysiologic criteria to provide a more specific diagnosis of DSPN.…”
“…Patients with DSP display a broad spectrum of PNS impairment, ranging from degeneration of long axons ( Pardo et al, 2001 ) and dorsal root ganglia ( Bradley et al, 1998 ) to damage of the gracile tracts ( Rance et al, 1988 ) and both myelinated and unmyelinated fibres ( Araujo et al, 2000 ) .…”
The aim of this work was first to determine whether the cutaneous silent period (CSP), a marker of small-nerve-fibre function, was altered in human immunodeficiency virus (HIV)-positive subjects with predominantly sensory symmetrical polyneuropathy and, second, to assess whether such alterations were predictive of an impairment in the largest calibre sensory and motor nerve fibres of the upper limb (UL) peripheral nerves. CSP was assessed in three groups of subjects: healthy control subjects, HIV-positive subjects with peripheral neuropathy (PN) of the lower limbs, and HIV-positive patients with clinical and neurophysiological involvement of the four limbs. CSP study showed a significant increase of the latency compared to the controls both in HIV-positive cases with no impairment in the UL (p=0.006) and in patients with four-limb neuropathy (p=0.002). CSP study in HIV-positive patients with mild lower limb distal sensory polyneuropathy can detect an early involvement of the UL peripheral nerves. CSP latency increase could therefore be addressed as the first sign of PN spreading to the UL.
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