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Severe Hypernatremia as Presentation of Netherton Syndrome.
Glob Med Genet
December 2023
Department of Clinical and Experimental Medicine, University of Catania, Catania CT, Italy.
Article Synopsis
- Netherton syndrome is a rare genetic skin disorder marked by three main features: congenital ichthyosis (dry skin), immune system issues, and problems with the scalp.
- A case study details a 1-month-old boy who experienced severe health challenges, including failure to thrive and feeding problems, as well as an abnormal high sodium level at birth.
- The condition is caused by a mutation in the SPINK5 gene, leading to a protein deficiency that weakens the skin barrier, resulting in serious complications like skin infections and growth issues in infants.
Children atopic dermatitis: Diagnosis, mimics, overlaps, and therapeutic implication.
Dermatol Ther
December 2022
Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Atopic dermatitis (AD) is a chronic inflammatory, itching skin with a significant psychosocial impact on patients and relatives. In adults and adolescents besides flexural eczema, head and neck eczema, and hand eczema, which are the most frequent clinical phenotypes (84.9% and 84.
View Article and Find Full Text PDFA case of erythrodermia from exacerbated psoriasis vulgaris due to treatment of acute hepatitis C.
BMC Dermatol
May 2016
Division of Infectious Diseases and Hospital Hygiene, Cantonal Hospital St.Gallen, Rorschacherstrasse 95, 9007, St.Gallen, Switzerland.
Background: Skin side effects during interferon-alpha and ribavirin treatment are common, but autoimmune dermatosis triggered by interferon-alpha is rare. We describe a case of erythrodermia from exacerbated psoriasis during the treatment of acute hepatitis C with pegylated-interferon-alpha and ribavirin. The incidence of psoriasis in this circumstance is unknown and only 36 cases are described in the literature, of which only one describes an erythrodermic psoriasis flare.
View Article and Find Full Text PDF[A typical erythrodermia].
Rev Med Interne
January 2017
Service de médecine interne, hôpital Nord, Assistance publique des Hôpitaux de Marseille (AP-HM), chemin des Bourrely, 13915 Marseille cedex 15, France. Electronic address:
Erythrodermic lymphomatoid granulomatosis: a case report.
Case Rep Dermatol
September 2011
Department of Dermatology, Shimane University Faculty of Medicine, Izumo.
A 70-year-old man was admitted to our hospital for evaluation of a rapidly progressive erythrodermia. He had superficial lymph node swelling and gluteal/inguinal nodosum-like lesions. A skin biopsy of the erythrodermia showed dense mixed infiltrates distributed throughout the whole dermis, predominantly consisting of small lymphocytes and histiocytes with multinucleated giant cells presenting with a granulomatous appearance.
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