Results 71 to 80 of about 9,543 (240)

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda, B. Tedbirt, C. Bodemer, M. C. Bolling, M. El Hachem, M. Nikolić, E. Benton, M. Caproni, D. De, D. Didona, K. Drenovska, M. Goebeler, M. Hertl, B. Horváth, M. Kasperkiewicz, D. Kiritsi, M. Larralde, A. V. Marzano, J. Meijer, D. F. Murrell, J. Powell, E. Sprecher, N. S. Chandran, M. M. Tomayko, S. Uzun, N. van Beek, H. Ott, A. Patsatsi, A. Torrelo, A. Welfringer‐Morin, E. Schmidt, P. Joly   +31 more
wiley   +1 more source

Acrodermatitis enteropathica

British Journal of Dermatology, 1979
The first publication identifying acrodermatitis enteropathica as a definite disease (Danbolt & Closs, 1942) is reviewed. Later studies are briefly surveyed, resulting in the recognition of the disease as a zinc deficiency which can be effectively corrected by administration of small oral doses of zinc.
openaire   +4 more sources

Primary Cutaneous B‐Cell Lymphomas: An Updated Portrait of Classification, Biology, and Clinical Management

European Journal of Haematology, Volume 116, Issue 2, Page 116-128, February 2026.
ABSTRACT Primary cutaneous B‐cell lymphomas (CBCL) represent a clinically and biologically heterogeneous group of extranodal non‐Hodgkin lymphomas confined to the skin at the time of diagnosis. They account for approximately 25% of all primary cutaneous lymphomas and are subclassified into distinct entities according to the World Health Organization ...
A. Bernardelli, E. Carazzai, B. Bugnotto, F. Bellinato, M. Krampera, C. Visco   +5 more
wiley   +1 more source

Clinical analysis of 20 cases of childhood acrodermatitis enteropathica

Pifu-xingbing zhenliaoxue zazhi
Objective To investigate the clinical features of acrodermatitis enteropathica (AE). Methods A retrospective analysis was conducted on the clinical data of 20 children diagnosed with acrodermatitis enteropathica in the outpatient clinic at the ...
Jibing LI, Wei LI, Cui HU, Yingying QIAN, Ting ZHANG, Yafen WU, Hua QIAN   +6 more
doaj   +1 more source

Nutritional deficiency dermatitis related to branched-chain amino acid restriction in a child with maple syrup urine disease [PDF]

, 2019
We present a one-year-old girl with maple syrup urine disease with dermatitis secondary to the restriction of amino acids as part of the treatment.
Campuzano-García, Andrés Eduardo, Castanedo-Cázares, Juan Pablo   +1 more
core  

Biologic therapy for acrodermatitis continua of Hallopeau: Successful treatment with secukinumab and review of the literature

Dermatologic Therapy, 2019
Acrodermatitis continua of Hallopeau (ACH) is a rare pustular psoriasis variant refractory to many conventional treatments. We report the successful treatment with secukinumab of a patient with a long history of ACH with marked onychodystrophy with frank
M. Galluzzo, S. D’adamio, M. Teoli, L. Bianchi, M. Talamonti   +4 more
semanticscholar   +1 more source

Borrelia Infections Under B Cell‐Depleting Therapies: A Systematic Review of Diagnostic Challenges and Outcomes With Special Focus on Neurological Forms

European Journal of Neurology, Volume 33, Issue 1, January 2026.
Neurological infections caused by Borrelia burgdorferi sensu lato and Borrelia miyamotoi are increasingly reported in patients receiving anti‐CD20 therapies and should be considered in cases presenting with neurological symptoms and cerebrospinal fluid pleocytosis.
Emilie Cardot‐Martin, Jean Baptiste Chanson, Cédric Lenormand, Pierre Boyer, Yves Hansmann, Jean Sibilia, Benoit Jaulhac, Marc Scherlinger   +7 more
wiley   +1 more source

Acrodermatitis enteropática adquirida: reporte de un caso y revisión de la literatura

Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2019
La acrodermatitis enteropática es un raro trastorno producido por la deficiencia de cinc, que puede ser heredada o adquirida. Se caracteriza por la presencia de lesiones en la piel distribuidas en zonas distales o alrededor de orificios, alopecia y ...
Liliana Bohórquez, Cristina María Uribe, Ana Cristina Ruiz   +2 more
doaj  

A case of acrodermatitis enteropathica

Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2022
Acrodermatitis enteropathica (AE) is a rare genetic autosomal recessive disorder of zinc deficiency which manifests in infancy with triad of peri-orificial skin rash, alopecia, and diarrhea. We report the case of an 8-month-old infant with dermatological
Pankaj Das, Sandeep Arora, Gautam Kumar Singh, Amit Bahuguna, Neelam Singh, Prachi Verma   +5 more
doaj   +1 more source

EQ-5D in skin conditions: an assessment of validity and responsiveness [PDF]

, 2014
Aims and objectives This systematic literature review aims to assess the reliability, validity and responsiveness of three widely used generic preference-based measures of health-related quality of life (HRQL), i.e., EQ-5D, Health Utility Index 3 (HUI3 ...
AFN Klassen, BF O’donnell, C Moberg, D Feeny, D Papaioannou, D Revicki, DF Cella, E Christophers, E Daudén, GH Guyatt, GR Barton, J Brazier, J Brazier, J Brazier, J Dowie, J Tosh, JE Brazier, John Brazier, K Reich, L Longworth, L Longworth, L Matusiak, Louise Longworth, M Herdman, NICE, NICE, NJ Bansback, P Dolan, P Swinburn, PCM Kerkhof Van De, R Brooks, R Shikiar, R Shikiar, RJ Lasek, S Weiss, SCR Weiss, SJ Walters, T Luger, V Brodszky, Yaling Yang   +39 more
core   +3 more sources