Comments on ‘Gait Disturbance Due to Foot Drop Is Refractory to Treatment in Nonsystemic Vasculitic Neuropathy'
Author(s) -
Michael P. Collins,
Robert D. M. Hadden
Publication year - 2014
Publication title -
european neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.573
H-Index - 77
eISSN - 1421-9913
pISSN - 0014-3022
DOI - 10.1159/000368224
Subject(s) - foot drop , refractory (planetary science) , gait disturbance , medicine , gait , physical medicine and rehabilitation , disturbance (geology) , foot (prosody) , surgery , biology , astrobiology , linguistics , philosophy , paleontology
Patient 13 had an erythrocyte sedimentation rate of 115 mm/h, exceeding the PNS guideline cutoff of 100 mm/h for NSVN. This patient should be presumed to have a systemic vasculitic neuropathy. In table 1 , the ‘diameter of artery with angiitis’ ranges from 75–600 μm (mean 270 μm). In five patients, affected arteries were 400–600 μm. For the 11 patients with ‘probable’ vasculitis, that is, no vessel exhibiting inflammatory vessel-wall damage, there would be no pathologic basis on which to ascertain the size of angiitisaffected vessels [2] . How did the authors determine the size of the involved vessels in these patients? Moreover, the tabulated vessel sizes are unexpectedly large. Almost all vessels in sural nerve biopsies are ≤ 300 μm [4] . In the two previous analyses of affected vessel size in NSVN, mean diameters were 98 ± 87 μm and 80 ± 31 μm [5, 6] . Can the authors explain these inconsistencies? What was the duration between the ‘initial’ and ‘final’ modified Rankin scale (mRS) assessment for each patient? Dear Sir, The article by Hirahara et al. describes retrospective observations on 16 patients with nonsystemic vasculitic neuropathy (NSVN) [1] . NSVN is a rare disorder with only eight series reporting clinical information on more than ten patients [2, 3] . A Peripheral Nerve Society (PNS) task force published a guideline on NSVN in 2010 [2] . As members of this task force, we have questions about this study. How did the authors distinguish between ‘polyneuropathy’ and ‘mononeuritis multiplex?’ How were diffuse polyneuropathies with asymmetric features categorized? How many patients had pain? In table 1 , only three had ‘myalgias’, but another three presented with lower limb pain. Were electrodiagnostic findings axonal or demyelinating? Two patients had ‘eruption’ as their first symptom. Cutaneous vasculitis excludes NSVN, which can be diagnosed only in the absence of extra-neurologic clinical involvement (pathologic involvement in muscle biopsy permitted). Received: June 11, 2014 Accepted: September 7, 2014 Published online: November 12, 2014
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