Neurophysiological comparative response to clinical and surgical treatment of the ulnar neuropathy in leprosy
DOI:
https://doi.org/10.11606/issn.2317-0190.v27i3a166868Keywords:
Ulnar Neuropathies, Leprosy, Neural ConductionAbstract
Leprosy neuropathy may develop into subacute and chronic inflammatory scenarios, called reactions, which may cause entrapments in the anatomic tunnels. Objective: This study describes the late nerve conduction findings in patients with ulnar neuropathy at the elbow that were submitted to clinical and surgery treatments. Methods: A total of 27 nerves of 21 patients with borderline leprosy during type 1 (reversal) reaction were selected in a non- competing retrospective cohort for three years. The nerves with treated clinically active neuropathy (Group A1) were randomized for inclusion of surgical treatment (Group A2) after one month of clinical treatment without clear signs of clinical and neurophysiological improvement. Fifteen nerves were randomly chosen for surgery while 12 were clinically treated, after steroids treatment without expected response. Nerve conduction was measured before and after treatment on four occasions. Results: The authors observed significant improvement in the following variables in the surgically treated nerves: compound motor action potential amplitude (CMAP) at elbow and above elbow and conduction velocity (CV) along the forearm. Conclusion: The improvement of CMAP amplitudes and conduction velocity (CV) along the forearm express the late effect of nerve decompression. Persistence of temporal dispersion (TD) along the elbow was related to the new reaction or to incomplete surgical solution. However, moderate reduction in CV along the elbow, without TD, was considered an indication of na expected partial remyelination. Previous gradation of the nerve lesion based on the CMAP amplitude was related to the most severe results.
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References
Garbino JA, Marques Jr W . A neuropatia da hanseníase. In: Alves ED, Ferreira TL, Ferreira IN (Org.). Hanseníase: avanços e desafios. Brasília: Editora UnB; 2014. p. 215-29.
Garbino JA, Virmond MCL, Ura S, Salgado MH, Naafs B. A randomized clinical trial of oral steroids for ulnar neuropathy in type1 and type 2 leprosy reactions. Arq. Neuropsiquiatr. 2008;66(4):861-7. Doi: https://doi.org/10.1590/S0004-282X2008000600016
Garbino JA, Heise CO, Marques Jr W. Assessing nerves in leprosy. Clin Dermatol. 2016;34(1):51-8. Doi: https://doi.org/10.1016/j.clindermatol.2015.10.018
Preston DC, Shapiro BE. Basic nerve conduction studies. In: Preston DC, Shapiro BE. Electromyography and neuromuscular disorders: clinical-electrophysiologic-ultrasound correlations. 4th ed. Philadelphia: Elsevier; 2020. p. 23-40.
Tankisi H, Pugdahl K, Fuglsang-Frederiksen A, Johnsen B, Carvalho M, Fawcett PR, et al. Pathophysiology inferred from electrodiagnostic nerve tests and classification of polyneuropathies. Suggested guidelines. Clin Neurophysiol. 2005;116(7):1571-80. Doi: https://doi.org/10.1016/j.clinph.2005.04.003
Garbino JA, Naafs B, Ura S, Salgado MH, Virmond M. Neurophysiological patterns of ulnar nerve neuropathy in leprosy reactions. Lepr Rev. 2010;81(3):206-15.
Uchida Y, Sugioka Y. Electrodiagnosis of Martin-Gruber connection and its clinical importance in peripheral nerve surgery. J Hand Surg Am. 1992;17(1):54-9. Doi: https://doi.org/10.1016/0363-5023(92)90113-4
Almeida JA, Vitti M, Garbino JA. Estudo anatômico da anastomose de Martin-Gruber. Hansen Int. 1999;24(1):15-20.
Kimura J. Fatos e falácias nos estudos de neurocondução. In: Kimura J. Eletrodiagnóstico em doenças de nervos e músculos: princípios e aspectos práticos. 4 ed. Rio de Janeiro: DiLivros; 2015. p. 211-41.
Duerksen F. Tratamento cirúrgico da neurite hansênica. In: Duerksen F, Virmond M. Cirurgia reparadora e reabilitação em hanseníase. Bauru: Instituto Lauro de Souza Lima; 1997. p. 107-18.
Srinivasan H, Palande DD. Essential surgery in Leprosy – techniques for district hospitals. Geneve: WHO; 1997.
Huang JH, Samadani U, Zager EL. Ulnar nerve entrapment neuropathy at the elbow: simple decompression. Neurosurgery. 2004;55(5):1150-3. Doi: https://doi.org/10.1227/01.neu.0000140841.28007.f2
Barreto J A, Carvalho CV, Cury Filho M, Garbino JA, Nogueira MES, Soares CT. Hanseníase multibacilar com baciloscopia dos esfregaços negativa: a importância de se avaliar todos os critérios antes de defi nir a forma clínica. Hansen Int. 2007;32(1): 75-9.
Dellon AL. Multiple Crush Concept Applied to Multiple Nerves in Leprous Neuropathy. Clin Podiatr Med Surg. 2016;33(2):203-17. Doi: https://doi.org/10.1016/j.cpm.2015.12.009
Andrade PR, Jardim MR, Silva AC, Manhaes PS, Antunes SL, Vital R, et al. Inflammatory Cytokines Are Involved in Focal Demyelination in Leprosy Neuritis. J Neuropathol Exp Neurol. 2016;75(3):272-83. Doi: https://doi.org/10.1093/jnen/nlv027
Mietto BS, Andrade PR, Jardim MR, Antunes SL, Sarno EN. Demyelination in Peripheral Nerves: Much to Learn from Leprosy Neuropathy. J Mult Scler. 2016;3(2):174. Doi: https://doi.org/10.4172/2376-0389.1000174
Jessen KR, Mirsky R. The repair Schwann cell and its function in regenerating nerves. J Physiol. 2016;594(13):3521-31. Doi: https://doi.org/10.1113/JP270874
Burns PB, Kim HM, Gaston RG, Haase SC, Hammert WC, Lawton JN, et al. Predictors of functional outcomes after simple decompression for ulnar neuropathy at the elbow: a multicenter study by the SUN study group. Arch Phys Med Rehabil. 2014;95(4):680-5. Doi: https://doi.org/10.1016/j.apmr.2013.10.028
Antunes SL, Chimelli L, Jardim MR, Vital RT, Nery JA, Corte-Real S, et al. Histopathological examination of nerve samples from pure neural leprosy patients: obtaining maximum information to improve diagnostic efficiency. Mem Inst Oswaldo Cruz. 2012;107(2):246-53. Doi: https://doi.org/10.1590/s0074-02762012000200015
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