Results 41 to 50 of about 3,128 (178)

Palmoplantar pustulosis: pathogenesis, differential diagnosis, and treatment

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 516-535, April 2026.
Summary Palmoplantar pustulosis (PPP) is a chronic inflammatory and often painful disease characterized by sterile pustules on the palms and soles, significantly impairing quality of life. Women are more frequently affected than men, and smoking is a major trigger. Under biologic therapies, especially TNF antagonists, a paradoxical PPP may occur.
Rotraut Mössner, Tanja Fetter, Robert Sabat, Ulrich Mrowietz, Neda Cramer, Dagmar Wilsmann‐Theis   +5 more
wiley   +1 more source

Complications and Laboratory Test Findings Among Patients With Generalized Pustular Psoriasis: A Retrospective Chart Review Study

Experimental Dermatology, Volume 35, Issue 3, March 2026.
ABSTRACT Generalized pustular psoriasis (GPP) is a rare, chronic, inflammatory skin disease characterised by widespread eruption of sterile, macroscopic pustules. Patients with GPP can present with multiple comorbidities that may influence treatment. This study aimed to assess the frequency of psoriasis‐related complications and non–psoriasis‐related ...
Ryuhei Okuyama, Yukari Okubo, Shinichi Imafuku, Yayoi Tada, Keiichi Yamanaka, Kazumitsu Sugiura, Yukie Yamaguchi, Masahito Yasuda, Wataru Sakamoto, Morihisa Saitoh, Akimichi Morita   +10 more
wiley   +1 more source

Acrodermatitis Enteropathica

Medicine, 2016
Acrodermatitis enteropathica is a rare genetic autosomal recessive disorder, characterized by periorificial dermatitis, alopecia, and diarrhea. It is caused by mutations in the gene that encodes a membrane protein that binds zinc. We report a 14-month-old boy, admitted for erythematous, scaly and pustular lesions, initially located in the inguinal and ...
Nistor, Nicolai, Ciontu, Lavinia, Frasinariu, Otilia-Elena, Lupu, Vasile Valeriu, Ignat, Ancuta, Streanga, Violeta   +5 more
openaire   +2 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

Hereditary Acrodermatitis Enteropathica In Two Siblings

Indian Journal of Dermatology, 2003
Acrodermatitis enteropathica is a rare hereditary disorder of zinc metabolism characterized by dermatitis involving the acral and periorificial skin, diarrhea and growth retardation. Two siblings with classical features of acrodermatitis enteropathic and
Masood Quzi, Majid Imran
doaj  

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 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

An 11‐Month‐Old Infant With Unusual Diaper Dermatitis

JEADV Clinical Practice, Volume 5, Issue 2, Page 731-733, June 2026.
Majda Chaoui, Léo‐Paul Secco, Ifigenia Spanoudi‐Kitrimi   +2 more
wiley   +1 more source

Nutritional Deficiencies Following Bariatric Surgery: A Rapid Systematic Review of Case Reports of Vitamin and Micronutrient Deficiencies Presenting More Than Two Years Post‐Surgery

Clinical Obesity, Volume 15, Issue 6, December 2025.
ABSTRACT Bariatric surgery is the most clinically‐ and cost‐effective intervention for severe obesity. However, without adequate follow‐up, it can lead to nutritional deficiencies. Patients require life‐long nutritional supplements and follow‐up to prevent nutritional deficiencies from developing.
Sophie Haughton, Sarah Gentry, Helen M. Parretti   +2 more
wiley   +1 more source

Micronutrient deficiencies after pancreatico‐duodenectomy: A narrative review of the literature and recommendations for clinical practice

Nutrition in Clinical Practice, Volume 40, Issue 5, Page 1073-1092, October 2025.
Abstract Micronutrient uptake is impaired after pancreatico‐duodenectomy (PD) because of malabsorption, reduced absorptive capacity, and poor oral intake. Biochemical depletion is reported in cohort studies, but deficiency states are predominantly reported in case reports, making it difficult to assess occurrence rates.
Mary E. Phillips, Callum Livingstone, Adam E. Frampton, Kathryn H. Hart   +3 more
wiley   +1 more source