Open AccessEarly onset of scleromyxedema Arndt‐Gottron associated with a monoclonal gammapathy: Successful treatment with intravenous immunoglobulins
Author(s) -
Kefi Asma,
Jaziri Fatima,
Ben Abdelghani Khaoula,
Turki Sami
Publication year - 2022
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.6122
Subject(s) - medicine , dermatology , intravenous immunoglobulins , monoclonal , paraproteinemias , monoclonal gammopathy , monoclonal antibody , immunology , antibody
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 scleromyxedema case associated with a benign monoclonal gammapathy in an old woman.