| Literature DB >> 17958777 |
Monica Sanchez-Ross1, Renée Snyder, María I Colome-Grimmer, Mark Blumberg, Yve Huttenbach, Sharon Raimer.
Abstract
Nephrogenic fibrosing dermopathy is a recently recognized skin disorder similar in appearance to scleromyxedema but without the systemic involvement. We describe a 14-year-old girl with new-onset systemic lupus erythematosus and acute lupus nephritis who developed on the lower extremities confluent hyperpigmented, woody, indurated plaques that contained groups of coalescing erythematous papules. Nephrogenic fibrosing dermopathy was diagnosed histologically. Possible etiologies are discussed.Entities:
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Year: 2007 PMID： 17958777 DOI： 10.1111/j.1525-1470.2007.00437.x
Source DB: PubMed Journal: Pediatr Dermatol ISSN： 0736-8046 Impact factor: 1.588