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http://dx.doi.org/10.1503/cmaj.180868 | DOI Listing |
Clin Exp Dermatol
September 2022
Department of Dermatology, Venereology, and Leprosy, IMS and SUM Medical College Hospital, Bhubaneshwar, India.
Erythroderma is usually attributed to some of the commoner causes such as eczematous disorders, psoriasis, malignancies, idiopathic situations and drug-induced scenarios. Rarely, erythroderma has been found to result from dermatophytic infections. Erythrodermic dermatophytosis may be a direct sequel of extensive tinea corporis (with or without a background of topical steroid misuse), paraneoplastic phenomenon, an id reaction or congenital erythrodermic disorders, with subsequent development of dermatophytosis.
View Article and Find Full Text PDFBMJ Case Rep
May 2021
Department of Cellular Pathology, North Bristol NHS Trust, Westbury on Trym, UK.
A young woman presented with mucocutaneous blisters and ulcerating lesions, and was diagnosed with erythrodermic pemphigus complicated by bronchiolitis obliterans. Her clinical condition did not improve on immunosuppressive therapy. She had a history of an asymptomatic retroperitoneal mass, presumed to be a dermoid cyst, followed up clinically.
View Article and Find Full Text PDFDermatol Online J
July 2020
Department of Dermatology, University of Arkansas for Medical Sciences, Little Rock, AK.
We present a patient with erythrodermic Darier disease occurring in temporal association with diagnosis of metastatic lung adenocarcinoma. The patient presented with eroded and crusted keratotic papules and plaques over greater than 90% body surface area with extensive secondary impetiginization. Given a longstanding history of pruritic eruption, this presentation represents a paraneoplastic flare of an underlying genodermatosis.
View Article and Find Full Text PDFSci Rep
June 2020
Division of Clinical Dermatology, Hospital das Clínicas, University of São Paulo Medical School, São Paulo, Brazil.
Erythroderma is characterized by erythema and scaling affecting more than 80% of the body surface area. It is potentially life-threatening, and diagnosis of the underlying disease is a challenge. Despite laboratory improvements, many cases remain idiopathic.
View Article and Find Full Text PDFCMAJ
December 2018
Department of Medicine, University of Toronto, Toronto, Ont.
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