Literature DB >> 27119000

Erythroderma. A clinical and etiological study of 103 patients.

Artur César1, Maria Cruz1, Alberto Mota1, Filomena Azevedo2.   

Abstract

BACKGROUND: Erythroderma is an uncommon and severe dermatological manifestation of a variety of diseases. It is commonly challenging to find the underlying cause.
OBJECTIVE: The aim of this study was to analyze the causes of the disease in patients with erythroderma. PATIENTS AND METHODS: Data including the clinical symptoms, laboratory examinations, histopathology and follow-up information were collected from patients with erythroderma admitted to our department between 2000 and 2010.
RESULTS: One-hundred and three patients diagnosed with erythroderma were identified during this period (11.9% of all hospitalized patients; hospital incidence = 9.4 cases/year). The mean age of onset was 54.4 years (range: 17-89 years) with a male:female ratio of 1.5:1. The most frequent cause of erythroderma was exacerbation of preexisting dermatoses (65.0%), including psoriasis (44.7%) and eczema (16.5%). Drugs (18.4%) and cutaneous T-cell lymphomas (11.7%) induced most of the remaining cases. No cause could be identified in four cases (3.9%). Apart from erythema and scaling, that were present in all patients, clinical findings were dominated by pruritus (97.1%), followed by edema (56.3%), fever (54.4%), palmoplantar keratoderma (50.5%), nail changes (42.7%), liver or spleen enlargement (41.7%) and lymphadenopathy (40.8%).
CONCLUSIONS: Although numerous clinical features and laboratory values were abnormal, most findings were non-specific. The skin biopsy yielded a positive clinical correlation in most cases. Our study had a high percentage of erythroderma secondary to preexisting skin disease and a relatively low percentage of idiopathic erythroderma.

Entities:  

Keywords:  dermatitis; erythroderma; exfoliative; psoriasis

Year:  2016        PMID: 27119000      PMCID: PMC4844528          DOI: 10.3315/jdcr.2016.1222

Source DB:  PubMed          Journal:  J Dermatol Case Rep        ISSN: 1898-7249


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