Early onset of scleromyxedema Arndt‐Gottron associated with a monoclonal gammapathy: Successful treatment with intravenous immunoglobulins

Abstract Arndt‐Gottron (S‐AG) syndrome or scleromyxedema is a scarce disease characterized by a generalized papular and sclerodermoid eruption and systemic manifestations that can lead to significant morbid‐mortality. Interesting, S‐AG can be associated with a paraprotein. We report an exceptional s...

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Bibliographic Details
Main Authors: Asma Kefi, Fatima Jaziri, Khaoula Ben Abdelghani, Sami Turki
Format: Article
Language:English
Published: Wiley 2022-08-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.6122