Results 101 to 110 of about 6,111 (249)

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

Recalcitrant pityriasis rubra pilaris in a Middle Eastern patient and arguments for early anti‐IL‐23 targeting

open access: yesJEADV Clinical Practice
Pityriasis rubra pilaris (PRP) is a rare, chronic cutaneous inflammatory disorder of keratinization affecting adults, children and patients with HIV. The pathogenesis of PRP is not fully understood with clinical presentations, and severity remains highly
M. N. Al-Abdulla   +8 more
semanticscholar   +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

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 and HIV: a diagnostic challenge-case report and critical review of the literature [PDF]

open access: yes
Pityriasis rubra pilaris (PRP) is a rare cutaneous disorder characterized by hyperkeratotic follicular papules and palmoplantar keratoderma. Its clinical presentation ranges from mild to severe forms, including erythroderma.
Amador-Eleuterio, Sarahi   +3 more
core   +2 more sources

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.

open access: yesDermatology online journal, 2013
Pityriasis rubra pilaris (PRP) is an inflammatory condition of uncertain etiology. We present a case of PRP that demonstrates acantholysis on histopathologic examination, which is a characteristic feature that increasingly is recognized to aid in the diagnosis. We also review the clinical presentations and treatment options for this condition.
Marie, Leger   +5 more
openaire   +3 more sources

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

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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