Results 51 to 60 of about 7,109,345 (167)

Complications oesophagiennes d'un cas observé d'épidermolyse bulleuse congénitale de type Hallopeau-Siemens

open access: yes, 2002
La forme dystrophique récessive de type Hallopeau-Siemens est certainement la forme la plus grave des épidermolyses bulleuses congénitales. La gravité de l'atteinte cutanée est majeure, aboutissant après quelques années d'évolution chez l'enfant atteint,
CAMPIONE, Laurent   +1 more
core  

Successful treatment of severe acrodermatitis continua of hallopeau with Bimekizumab: A case report

open access: yes
Acrodermatitis continua of Hallopeau is a rare form of pustular psoriasis affecting the acral fingers and toes, characterized by recurrent eruptions of sterile pustules that lead to significant pain and potentially irreversible destruction of the nail ...
Kaiyang Li   +3 more
core   +1 more source

An Acrodermatitis continua of hallopeau evolving into generalized pustular psoriasis: A case series

open access: yes, 2022
Acrodermatitis continua of Hallopeau (ACH) is considered as a variant of localized pustular psoriasis which involves fingertip and nail. ACH is rarely reported to evolve into generalized pustular psoriasis (GPP).
Haken Tenizar   +3 more
core   +1 more source

Case Report: Paradoxical acrodermatitis of Hallopeau-like eruption following anti-IL-17 therapy [PDF]

open access: yes, 2019
Psoriasis is a chronic immune-mediated inflammatory disease. Up to 40% of patients with psoriasis may develop psoriatic arthritis. Currently, interleukin (IL)-17/IL-23 pathways are identified as key factors in the immunopathogenesis of both conditions ...
Tadiotto Cicogna, Giulia   +4 more
core   +1 more source

Correlation of IL36RN mutation with different clinical features of pustular psoriasis in Chinese patients

open access: yes, 2017
Different studies have reported various values for the percentage of patients with IL36RN mutations, and it has also been reported that the sites of these mutations differ among different ethnicities.
蔡呈芳;詹智傑;邱顯鎰;林頌然;洪楨邦;王鼎舜   +1 more
core   +1 more source

Nails as immune-privileged sites: A case of disabling Acrodermatitis continua of Hallopeau successfully treated with Apremilast

open access: yes, 2019
Acrodermatitis continua of Hallopeau (ACH) is a chronic, inflammatory, and relapsing disorder characterized by the progressive destruction of fingernails and toenails. This condition is rare, difficult to treat, and often misdiagnosed.
Cesaroni, Gaia Maria   +15 more
core   +1 more source

Genotype–Phenotype Correlations and Clinical Outcomes of Spesolimab in Acrodermatitis Continua of Hallopeau: A Multicenter Retrospective Cohort Study

open access: yesPsoriasis: Targets and Therapy
Xuan Deng,1,* Yusha Chen,2– 4,* Xinli Liu,1 Jianxia Xiong,1 Runlu Hu,1 Sijian Liao,1 Wei Li,3,4 Kun Huang11Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People’s Republic of China ...
Deng X   +7 more
doaj  

Pustular psoriasis

open access: yes, 2016
A number of pustular skin diseases share clinical, pathogenetic, and epidemiological aspects with plaque-type psoriasis, and their classification as a separate clinical entity or as a subtype of psoriasis remains controversial, which is also reflected in
Kahl, Christoph   +9 more
core   +1 more source

СТОЙКИЙ ГНОЙНЫЙ АКРОДЕРМАТИТ АЛЛОПО В СОЧЕТАНИИ С ОГРАНИЧЕННЫМ ВУЛЬГАРНЫМ ПСОРИАЗОМ [PDF]

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 ...
 Gordeeva A.A.   +5 more
core   +1 more source

Акродерматит Аллопо - клиническая разновидность ладонно-подошвенного пустулезного псориаза?

open access: yes, 2020
Pustular palmar-plantar psoriasis has a number of clinical variants. Dermatologists describe it as independent diseases, for example, acrodermatitis continua suppurativa Hallopeau, etc. The aim of the study was a clinical and laboratory evaluation of two
Turykina E.A.   +3 more
core  

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