Case report of Sleromyxedema with sensory motor axonal polyneuropathy treated with immunoglobulin therapy


Case Report

Author Details : Rakesh Kumar Jagdish*

Volume : 9, Issue : 1, Year : 2022

Article Page : 37-39

https://doi.org/10.18231/j.agems.2022.008



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Abstract

Sleromyxedema is a rare disease characterised by extensive mucin deposition with fibrosis in dermis. It is often associated with monoclonal gammopathy. Its true prevalence and/or cause is unknown due to its rarity. Various extra-cutaneous manifestations can be associated with sleromyxedema such as dermoneuro syndrome, neuropathy, rheumatological problems or various malignancies. This case report showed that a patient with sleromyxedema and neuropathy had positive outcomes when treated with intravenous immunoglobulin (IVIg) and steroids pulses. The underlying cause of the patient’s condition was unknown.


Keywords: Sleromyxedema, Immunoglobulin therapy, Dermoneuro syndrome, Sensory Motor Axonal Polyneuropathy, Monoclonal Gannopathey


How to cite : Jagdish R K, Case report of Sleromyxedema with sensory motor axonal polyneuropathy treated with immunoglobulin therapy. Ann Geriatr Educ Med Sci 2022;9(1):37-39


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Article History

Received : 25-05-2022

Accepted : 10-06-2022


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Article DOI

https://doi.org/10.18231/j.agems.2022.008


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