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Review
. 2022 Jul;269(7):3779-3788.
doi: 10.1007/s00415-022-11007-z. Epub 2022 Feb 15.

Peripheral neuropathy and livedoid vasculopathy

Antoine Soulages  1 , Thierry Maisonobe  2 , Pascal Auzou  3 , Antoine Petit  4 , Yves Allenbach  5 , Stéphane Barète  6 , Sophie Skopinski  7 , Emmanuel Ribeiro  8 , Marie-Laure Jullié  9 , Laurence Lamant  10 , Françoise Brevet  11 , Xavier Soulages  12 , Jean-Michel Vallat  13 , Marie-Laure Martin-Négrier  14 , Guilhem Solé  1 , Fanny Duval  1 , Louis Carla  1 , Gwendal Le Masson  1 , Stéphane Mathis  15
Affiliations
Review

Peripheral neuropathy and livedoid vasculopathy

Antoine Soulages et al. J Neurol. 2022 Jul.

Abstract

Background: Livedoid vasculopathy (LV) is a chronic dermatosis associated with micro-thrombosis of the vessels of the dermis, leading to ischemic lesions and painful skin ulcerations of the lower limbs. This thrombosing occlusive vasculopathy, clearly distinct from 'classical vasculitis' (not related to alteration of vessel walls), may lead to peripheral neuropathy.

Objective: To clarify the main clinical, electrophysiological and pathological characteristics of peripheral neuropathy linked to LV.

Method: We presented a series of personal cases of peripheral neuropathy due to LV. We also conducted a review of the literature (since the first description of LV in 1974) using multiple combinations of keywords from 'PubMed', 'Google Scholar' and 'ScienceDirect' databases according to the 'Preferred Reporting Items for Systematic reviews and Meta-Analyses' guidelines.

Results: We identified 16 patients (6 personal cases and 10 cases from the medical literature). Our personal cases were five females and one male, with a median age (at the onset of cutaneous signs of LV) of 38 (range 25-62). Several types of skin lesions of the lower limbs were observed. Median age at the onset of peripheral neuropathy symptoms was 48 years (range 29-66), with a main clinical and electrophysiological pattern of mononeuropathy multiplex.

Discussion: We observed a typical pattern of peripheral neuropathy, mostly mononeuropathy multiplex, whose pathophysiology might be related to occlusions of the small vessels of the nerves, as seen in the dermis. Moreover, LV may also be associated with other types of peripheral neuropathies (sometimes of autoimmune etiology) not directly related to the skin lesions.

Conclusion: The 'ischemic form' of peripheral neuropathy linked to LV is mainly responsible for sensory disturbances (with multifocal distribution), sometimes for motor disturbances. This type of peripheral neuropathy has to be distinguished from 'classical vasculitic neuropathies' which are usually treated with antithrombotic therapies.

Keywords: Livedoid; Mononeuropathy; Peripheral neuropathy; Vasculitis; Vasculopathy.

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