Results 51 to 60 of about 3,355 (200)

Acute Generalized Exanthematous Pustulosis Associated with Diltiazem [PDF]

open access: yes, 2008
Acute generalized exanthematous pustulosis (AGEP) usually presents with the acute appearance of oedematous and erythematous lesions, on which multiple sterile pustules appear, associated with fever.
Caldas Lopes, L   +4 more
core  

Acute Localized Exanthematous Pustulosis on the Face [PDF]

open access: yes, 2011
Acute localized exanthematous pustulosis (ALEP) is a localized variant of acute generalized exanthematous pustulosis, which is characterized by the eruption of multiple scattered pustules following drug administration.
Betto   +20 more
core   +2 more sources

Line-field confocal optical coherence tomography: a new tool for non-invasive differential diagnosis of pustular skin disorders [PDF]

open access: yes, 2022
Background The spectrum of pustular skin disorders (PSD) is large and particularly challenging, including inflammatory, infectious and amicrobial diseases.
Cinotti, E   +6 more
core   +1 more source

Successful Use of Bimekizumab in Refractory Acute Generalised Exanthematous Pustulosis Triggered by Amoxicillin‐Clavulanate

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Acute generalised exanthematous pustulosis (AGEP) is a rare, acute neutrophilic dermatosis most commonly triggered by drugs, which typically resolves within 2 weeks following withdrawal of the causative agent. Topical and systemic corticosteroids remain the standard treatment.
Alexandra Junge   +5 more
wiley   +1 more source

Cephalexin-induced acute generalized exanthematous pustulosis

open access: yesDermatology Reports, 2018
Cephalexin is a cephalosporin antibiotic that is commonly used in the treatment of infectious diseases. We report a patient exhibiting a rare adverse effect of cephalexin: drug-induced Acute Generalized Exanthematous Pustulosis (AGEP).
Matthew DaCunha   +2 more
doaj   +1 more source

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents

open access: yesJournal of the European Academy of Dermatology and Venereology, EarlyView.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda   +31 more
wiley   +1 more source

Lapatinib-induced acute generalized exanthematous pustulosis

open access: yesIndian Dermatology Online Journal, 2010
Acute generalized exanthematous pustulosis (AGEP) is a pustular eruption, mainly drug induced often accompanied by fever and neutrophilic leukocytosis presenting as scarlatiniform erythema over the flexures evolving into numerous tiny non follicular ...
Chembolli Lakshmi   +2 more
doaj   +1 more source

Pustular Psoriasis and Acute Generalized Exanthematous Pustulosis

open access: yesMedicina, 2021
The similarity between pustular psoriasis (PP) and acute generalized exanthematous pustulosis (AGEP) poses problems in the diagnosis and treatment of these two conditions. Significant clinical and histopathologic overlap exists between PP and AGEP. PP is
Morgan Sussman   +5 more
doaj   +1 more source

Systemic loxoscelism - a unique cause of acute generalized exanthematous pustulosis : a case series [PDF]

open access: yes, 2023
Introduction: Acute Generalized Exanthematous Pustulosis (AGEP) is a rare, severe cutaneous eruption characterized by the numerous pustules on an erythematous base.
Bohnert, Mike   +4 more
core   +1 more source

Superficial Pustular Folliculitis of the Face and Neck—A Non‐Infectious Eruption Responding to Topical Steroids

open access: yesJEADV Clinical Practice, Volume 4, Issue 5, Page 1057-1067, December 2025.
Twenty‐seven young patients, mostly females, presenting with monomorphous, discrete, tiny, superficial follicular pustules on the face (44.4%), the face and neck (51.8%) and the neck (3.7%). The eruption was itchy in 44.4%, recurrent in 81% of cases and responded well to topical corticosteroids. Histopathologic findings of 3 cases revealed infundibular
Hui‐Peng Huang   +4 more
wiley   +1 more source

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