Results 31 to 40 of about 7,109,345 (167)

Acrodermatite continua di Hallopeau [PDF]

open access: yes, 2009
L’acrodermatite continua di Hallopeau (ACH) è una rara patologia cutanea cronico-ricorrente che coinvolge la porzione distale delle dita di mani e piedi.
Bidoli, A.   +9 more
core   +1 more source

Efficacy and safety of TNF blockers and of ustekinumab in palmoplantar pustulosis and in acrodermatitis continua of Hallopeau

open access: yes, 2020
International audiencePalmoplantar pustulosis (PPP) and acrodermatitis continua of Hallopeau (ACH) are rare variants of psoriasis.
d'Incan, M.   +47 more
core   +1 more source

Pênfigo vegetante de hallopeau em puerpério imediato: relato de caso e breve revisão de literatura/ Hallopeau vegetant pemphigus in immediate puerperia: case report and brief literature review [PDF]

open access: yes, 2022
O pênfigo de Hallopeau é uma enfermidade do grupo dos pênfigos vegetantes, sendo estes, variantes raras do pênfigo vulgar. Clinicamente, o pênfigo vegetante de Hallopeau manifesta-se com pústulas que, normalmente, evoluem com a formação de placas ...
França, Amanda Ribeiro   +3 more
core  

ACRODERMATITIS CONTINUA SUPPURATIVA HALLOPEAU IN COMBINATION WITH LOCALIZED PSORIASIS VULGARIS

open access: yes, 2017
А clinical case of a rare form of pustular psoriasis, known as “acrodermatitis continua suppurativa Hallopeau” is described. The involvement of the distal phalanges of the fingers and toes in combination with localized psoriasis vulgaris is observed ...
E. V. Sokolovskiy   +2 more
core   +1 more source

Acrodermatitis continua of Hallopeau response to optimized biological therapy [PDF]

open access: yes, 2019
Acrodermatitis continua of Hallopeau, first described in 1890, is an uncommon variant of pustular psoriasis. It presents as a sterile pustular eruption of the tips of fingers and toes.
Chaby, Guillaume   +10 more
core   +1 more source

Efficacy of adalimumab for the treatment of refractory paediatric acrodermatitis continua of hallopeau [PDF]

open access: yes, 2013
Acrodermatitis continua of Hallopeau (ACH) is a rare, chronic disease characterized by acropustular eruptions predominantly involving the distal phalanges of the hands and feet with marked involvement of the nail bed.
Barbanera, Sabrina   +2 more
core   +1 more source

Palmoplantare Pustulose: Entstehung, Differentialdiagnose und Therapie

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 516-536, April 2026.
Zusammenfassung Die palmoplantare Pustulose (PPP) ist eine chronisch entzündliche, häufig schmerzhafte Erkrankung mit sterilen Pusteln an Handflächen und Fußsohlen, die die Lebensqualität stark einschränkt. Frauen sind häufiger betroffen als Männer, und Rauchen ist ein bedeutender Provokationsfaktor.
Rotraut Mössner   +5 more
wiley   +1 more source

Acrodermatitis Continua of Hallopeau with Bone Resorption in an 8-Year-Old Patient: A Case Report [PDF]

open access: yes, 2017
Acrodermatitis continua of Hallopeau (ACH) is an uncommon inflammatory disease manifesting as sterile pustular eruption of the fingers and toes. The disease is of a chronic relapsing nature and is often refractory to treatment. With longstanding disease,
Mohammed Ayesh   +4 more
core   +1 more source

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

open access: yesExperimental 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   +10 more
wiley   +1 more source

Hereditary Epidermolysis Bullosa With KLHL24 Mutation Undergoing Heart Transplantation: A Case Report

open access: yesCase Reports in Surgery, Volume 2026, Issue 1, 2026.
Hereditary epidermolysis bullosa (EB) is a rare group of genetic diseases with structural and functional alterations affecting the epithelium leading to cell detachment with skin and mucosal epithelial damage. Certain EB subtypes are associated with an increased risk of cardiomyopathy.
Antonio Fiore   +5 more
wiley   +1 more source

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