1.
Am J Dermatopathol
; 40(4): 279-282, 2018 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28961556
RESUMO
Scleromyxedema is a rare disorder where patients may develop systemic manifestations such as monoclonal gammopathy, inflammatory polyarthritis, and esophageal and neurological dysfunction. Histologically, there may be atypical variants of scleromyxedema showing features resembling interstitial granuloma annulare. We report an unusual case of scleromyxedema with interstitial granulomatous pattern and highlight potential diagnostic pitfalls when encountered with such a variant.