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Sensory mononeuritis: differentiating pure neural leprosy from non-systemic vasculitic neuropathy
Author(s) -
Pinelopi Tsouni,
Johannes Alexander Lobrinus,
Andreas Steck,
Thierry Küntzer
Publication year - 2017
Publication title -
leprosy review
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 43
eISSN - 2162-8807
pISSN - 0305-7518
DOI - 10.47276/lr.88.2.274
Subject(s) - medicine , leprosy , mononeuritis multiplex , dapsone , nerve biopsy , neuritis , sensory neuropathy , skin biopsy , dermatology , sural nerve , vasculitis , systemic vasculitis , biopsy , peripheral neuropathy , surgery , pathology , disease , endocrinology , diabetes mellitus
We describe two cases of sensory mononeuritis that presented with similar past medical histories, and clinical and electrophysiological features. The two patients were females who had resided in areas endemic for leprosy (Brazil). Both developed a progressive, purely sensory, painful mononeuritis distally in the lower limbs with sensory nerve potentials asymmetrically reduced in amplitude. The sural nerve biopsy performed in Patient 1 showed granulomatous inflammation of the epineurial tissue, consistent with paucibacillary pure neural leprosy (PNL) while in Patient 2 there were signs of vascular inflammation consistent with non-systemic vasculitic neuropathy (NSVN). Patients 1 and 2 both improved following targeted treatment with rifampicin and dapsone vs. rituximab, respectively.

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