Results 41 to 50 of about 1,842 (159)

Refractory Palmoplantar Pustulosis Successfully Treated with JAK Inhibitor Tofacitinib: A Case Series

open access: yesInfection and Drug Resistance, 2023
Qingqing Xu,1 Xiaochen Wang,2 Anbo Yang,3 Guo Wei1 1Department of Dermato-Venereology, the Second Hospital of Shandong University, Jinan, 250033, People’s Republic of China; 2Clinical Laboratory of Qingdao Municipal Hospital, Qingdao, 266000, People’s ...
Xu Q, Wang X, Yang A, Wei G
doaj  

Cardiac structure and function in psoriasis: A cross‐sectional analysis of the PSOCADIA study

open access: yesJournal of the European Academy of Dermatology and Venereology, EarlyView.
Individuals with well‐treated psoriasis exhibited a higher burden of myocardial dysfunction (GLS < 16%) compared with controls, independent of cardiometabolic comorbidity. The prevalence was similar across psoriasis severity, highlighting the importance of cardiovascular assessment in all patients with psoriasis. Abstract Background Psoriasis is linked
Maria Dons   +16 more
wiley   +1 more source

Adalimumab-Induced Erythrodermic Psoriasis Associated with Alopecia in a Patient with Palmoplantar Pustulosis

open access: yesIndian Journal of Dermatology
In recent years, with the increased usage of tumour necrosis factor (TNF) inhibitors, more side effects have been revealed. Paradoxical psoriasis, including psoriasis vulgaris, palmoplantar pustulosis, scalp psoriasis and their combinations, is a common ...
Ying Wang, Yong Cui, Zhancai Zheng
doaj   +1 more source

Pustulotic arthro-osteitis (Sonozaki Syndrome)

open access: yesIndian Journal of Dermatology, 2011
Pustulotic arthro-osteitis, first described by Sonozaki, is a relatively rare disorder. Its prevalence is however probably underestimated in dermatological literature. Early recognition of the signs can prevent misdiagnosis. We describe a Turkish patient
Ozlem Su   +4 more
doaj   +1 more source

PUVA therapy for palmoplantar pustulosis

open access: yesActa Dermato-Venereologica, 1985
Forty patients suffering from pustulosis palmoplantaris were treated with PUVA therapy. Thirty-six patients had palmar lesions which cleared in 31 cases; in 18 cases after an initial course of 3 sessions of treatment per week during an average period of 10 weeks, and in another 13 only after additional, less frequent continuation of the PUVA therapy ...
S, Agren-Jonsson, E, Tegner
openaire   +2 more sources

Streptobacillosis characterised by palmoplantar pustulosis [PDF]

open access: yesThe Lancet Infectious Diseases, 2013
A 41-year-old French woman, with no previous medical history, presented with intermittent fever up to 40°C. 2 days later, palmoplantar pustules appeared (fi gure, A), as did cutaneous papules on her trunk and limbs. She had an oligoarthritis associated with the distal interphalangeal joint of the third left fi nger, the right knee, and both shoulders ...
Francois, Danion   +3 more
openaire   +2 more sources

Integrated Clinical Trial and Molecular Profiling Reveals Immune Drivers of Chronic Hand Eczema

open access: yesAllergy, Volume 81, Issue 8, Page 2815-2832, August 2026.
This study performed an unbiased molecular profiling of CHE patients across diverse etiologies to identify shared pathogenic drivers and evaluate the impact of IL‐4Rα blockade via dupilumab over 16 weeks. CHE shows a mixed immune signature involving type 1, 2, and 3 pathways with features of atopic dermatitis and psoriasis.
Perrine Gery   +25 more
wiley   +1 more source

Differentiation of Palmoplantar Psoriasis, Palmoplantar Pustulosis and Hyperkeratotic Palmoplantar Eczema Using Proteomic Analysis of Tape Strip Samples

open access: yesExperimental Dermatology, Volume 35, Issue 7, July 2026.
Tape strip‐based targeted proteomics reveals specific protein patterns in PPP compared with PP and HPE. The findings demonstrate the feasibility of tape strip proteomics to differentiate PPP from PP and HPE. ABSTRACT Palmoplantar inflammatory dermatoses, including hyperkeratotic palmoplantar eczema (HPE), palmoplantar psoriasis (PP) and palmoplantar ...
Mila B. Johansen   +7 more
wiley   +1 more source

Postpartum lumbopelvic pain could be SAPHO syndrome: a case report

open access: yesFrontiers in Immunology
BackgroundSynovitis–acne–pustulosis–hyperostosis–osteitis (SAPHO) syndrome is a rare autoimmune disorder. The involvement of spinal and sacroiliac joint in SAPHO syndrome closely resembles the manifestations of postpartum lumbopelvic pain (LPP).Case ...
Zheng Weiwei, Zhang Junhong, Zhang Rong
doaj   +1 more source

SAPHO Syndrome Presenting With Severe Inflammatory Back Pain (Sacroiliitis) and Rare Retinol Associated Myopathy in an Iraqi Adolescent Male: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT SAPHO syndrome is a rare autoinflammatory disorder characterized by synovitis, acne, pustulosis, hyperostosis, and osteitis. Although musculoskeletal and dermatologic manifestations are well recognized, extra‐articular involvement remains uncommon, particularly muscular inflammation.
Farah Jaafar Mahdi   +7 more
wiley   +1 more source

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