Results 91 to 100 of about 5,913 (240)

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation [PDF]

open access: yes, 2017
journal ...
74848   +17 more
core   +1 more source

Case Report of Dermatomyositis With Features of the Wong Variant Developing Post‐Trastuzumab Therapy for Breast Cancer

open access: yesAustralasian Journal of Dermatology, Volume 66, Issue 3, Page 183-185, May 2025.
ABSTRACT Drug‐induced dermatomyositis can be challenging to distinguish from paraneoplastic dermatomyositis. Rarely, antibodies directed against human epidermal growth factor receptor 2 (HER‐2), such as trastuzumab, may trigger dermatomyositis, and immune checkpoint inhibitors may incite the Wong variant of dermatomyositis, characterised by clinical ...
Lauren C. LaMonica   +3 more
wiley   +1 more source

Acquired erythroderma [PDF]

open access: yes, 2009
Erythroderma /exfoliative dermatitis/ is an inflammatory process affecting 90% of the total body surface area. Erythema, infiltration and desquamation are the main clinical features of the syndrome.
Broshtilova, V., Marina, S.
core   +2 more sources

Histopathological pattern of cutaneous disorders in tertiary care center in Shahjahanpur district of India [PDF]

open access: yes, 2020
Background: Histopathological examination is most commonly needed and used investigation in dermatology. The main objective of this study is to share our experience with skin lesions from a tertiary health Centre by describing the histopathological ...
Pant, Astha, Singh, Amar
core   +2 more sources

A Patient With Concurrent Hidradenitis Suppurativa and Porokeratosis Palmaris et Plantaris Disseminata: Case Report and Review of Autoinflammatory Keratinization Diseases

open access: yesJournal of Cutaneous Pathology, Volume 52, Issue 4, Page 272-277, April 2025.
ABSTRACT The term autoinflammatory keratinization diseases (AIKDs) was recently proposed as a unifying concept for diseases characterized by inflammation in the epidermis and upper dermis which leads to hyperkeratosis, caused by genetic perturbations of the innate immune system.
Meredith C. Rogers   +3 more
wiley   +1 more source

Pityriasis rubra pilaris‐like graft‐vs‐host disease following allogeneic stem cell transplant in two patients

open access: yesClinical Case Reports, 2019
Chronic cutaneous graft‐vs‐host disease (GVHD) has several atypical variants. We describe two cases of GVHD with clinical and histopathologic features of pityriasis rubra pilaris (PRP), which responded to additional immunosuppression. Recognition of this
Jennifer Y. Wang   +6 more
doaj   +1 more source

ERYTHRODERMIA: BETWEEN SKIN LYMPHOMA AND PITYRIASIS RUBRA PILARIS [PDF]

open access: yes, 2022
Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, Chişinău, Republica MoldovaIntroducere. Eritrodermia este definită ca un eritem generalizat, care implică mai mult de 90% din suprafața cutanată.
Bețiu, Mircea   +5 more
core  

Updated genetic background of generalized pustular psoriasis as an autoinflammatory keratinization disease

open access: yesThe Journal of Dermatology, Volume 52, Issue 3, Page 400-407, March 2025.
Abstract Generalized pustular psoriasis (GPP) is a severe autoinflammatory keratinization disease (AiKD) characterized by acute flares of widespread sterile pustules and high fever. GPP is potentially life‐threatening. Recently clarified genetic predisposing factors for GPP suggest that the excessive activation of innate immune pathways in the skin ...
Masashi Akiyama
wiley   +1 more source

Pityriasis rubra pilaris following administration of SARS‐CoV‐2 vaccine

open access: yesJournal of Cutaneous Immunology and Allergy, 2023
Pityriasis rubra pilaris (PRP) is a rare, chronic, inflammatory dermatosis characterized by follicular, hyperkeratotic papules and palmoplantar keratoderma at any age. The exact etiology of the disease remains unknown, but it can be triggered by multiple
Shumpei Kondo   +3 more
doaj   +1 more source

Advanced phasing techniques in congenital skin diseases

open access: yesThe Journal of Dermatology, Volume 52, Issue 3, Page 392-399, March 2025.
Abstract Phasing, the process of determining which alleles at different loci on homologous chromosomes belong together on the same chromosome, is crucial in the diagnosis and management of autosomal recessive diseases. Advances in long‐read sequencing technologies have significantly enhanced our ability to accurately determine haplotypes.
Ken Natsuga
wiley   +1 more source

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