1.
Clin Case Rep
; 10(8): e6122, 2022 Aug.
Artículo
en Inglés
| MEDLINE
| ID: mdl-35937020
RESUMEN
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.