نتایج جستجو برای: erythroderma
تعداد نتایج: 812 فیلتر نتایج به سال:
ABSTRACT Erythroderma is a severe skin disease that can be associated with serious metabolic disorders and so it requires immediate care. The difficulty with erythroderma lies in finding the underlying cause. Several studies in other countries, that reported a different incidence of each etiologic group. The aim of this study was to evaluate various causes of erythroderma in Gilan and compare ...
Results: On average, the etiological diagnosis was established 11 months after the onset of erythroderma. The underlying causes observed included immunodeficiency (30%), simple or complex ichthyosis (24%), Netherton syndrome (18%), and eczematous or papulosquamous dermatitis (20%). Five patients (10%) had erythroderma of unknown origin. The following parameters were of value in determining the ...
Pemphigus foliaceus (PF) represents an autoimmune blistering disease characterized by the disruption of epidermal intercellular adhesion proteins. Clinical findings include superficial crusted erosions in a seborrheic distribution; however, the disease can rarely present as an exfoliative erythroderma. Histopathologic findings include acantholysis with cleavage within the granular layer. Direct...
Cutaneous manifestations of haematological malignancies, although well recognized in acute monoblastic leukaemia and lymphoma, are relatively uncommon in primary myelodysplastic syndrome (MDS), which is a group of heterogeneous disorders formerly known as pre-leukaemia. Previously reported cases of skin involvement in this syndrome have been confined to a sub-type of MDS, namely chronic myelomo...
Vol. 25, No. 2, 2013 271 Received December 27, 2011, Revised July 31, 2012, Accepted for publication September 19, 2012 Corresponding author: María Luisa Martínez-Martínez, Department of Dermatology, University General Hospital of Albacete, falcó brothers, No. 37, 02006, Albacete, Spain. Tel: 34-967-59-71-00, Fax: 34-697-24-39-52, E-mail: mlmartinezm@ sescam.jccm.es This is an Open Access artic...
Erythroderma is an unusual cutaneous finding associated with dermatomyositis. There are only five cases of erythrodermic dermatomyositis reported in the English literature. We treated a case of erythrodermic dermatomyositis associated with a Bormann type 1 gastric cancer. The patient had a generalized, erythematous scaly eruption consistent with erythroderma and Gottron's papules as well as a h...
The profile of 247 patients with erythroderma during a 23 year period from January, 1962 through March, 1985, with a follow-up period ranging from 1 to 26 years were analysed. The patients presented with diffuse erythema, scaling and pruritus of more than 2 months' duration, and the age ranged from 16 to 60 years. Psoriasis was the most frequent underlying disease with an estimated frequency of...
Non-bullous congenital ichthyosiform erythroderma (NBCIE) is an autosomal recessive form of inherited icthyosis appears as fine white scales that gradually replace collodion membrane. This case report describes management of 5 years and 11-month-old child with NBCIE suffering from early childhood caries (ECC) under general anesthesia. How to cite this article: Choudhary R, Satish V. Dental Trea...
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