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January 17, 2026Dermato0 citationsOpen Access

Drug-Induced Acute Generalized Exanthematous Pustulosis: Mechanisms, Diagnosis, and Clinical Differentiation from Other Pustular Eruptions

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EZEsteban Zavaleta‐MonestelAEAudry Escudero-CorreaJMJeaustin Mora-Jiménez

Key Points

  • To synthesize current evidence on AGEP, including its pharmacological triggers and diagnostic criteria.
  • Conducted a literature search in multiple databases including PubMed and Scopus.
  • Included studies from 2000 to 2025 focusing on clinical features and immunological pathways.
  • Synthesis of evidence regarding diagnostic tools and clinical differentiation of AGEP.
  • β-lactam antibiotics are the most frequent triggers of AGEP.
  • Increased associations found with drugs like hydroxychloroquine and immune checkpoint inhibitors.
  • IL-36 activation and neutrophil recruitment are key immunopathogenic mechanisms.
  • Diagnosis accuracy improves with a structured approach using biomarkers and histopathological assessments.

Abstract

Background/Objectives: Acute generalized exanthematous pustulosis (AGEP) is a severe drug-induced cutaneous reaction characterized by the abrupt onset of sterile pustules, fever, neutrophilia, and a T cell-mediated type IVd hypersensitivity response. This narrative review synthesizes current evidence on pharmacological triggers, immunopathogenic mechanisms, diagnostic criteria, and differential diagnosis to provide a clinically oriented framework. Methods: A comprehensive literature search was conducted in PubMed/MEDLINE, Scopus, ScienceDirect, and SpringerLink for studies published between 2000 and 2025, complemented by selected clinical reference sources. Studies addressing clinical features, immunological pathways, pharmacovigilance signals, and diagnostic tools for AGEP were included. Synthesis of Evidence: β-lactam antibiotics remain the most frequent triggers, while increasing associations have been reported with hydroxychloroquine, targeted therapies, immune checkpoint inhibitors, psychotropic agents, and vaccines. Immunopathogenesis is driven by IL-36 activation, CXCL8/IL-8–mediated neutrophil recruitment, and IL36RN mutations, explaining overlap with pustular psoriasis. Diagnostic accuracy improves through integration of drug latency, clinical morphology, histopathology, biomarkers, and standardized tools such as the EuroSCAR score. Conclusions: AGEP is a complex pustular reaction induced by diverse drugs and amplified by IL-36-mediated inflammation. Accurate diagnosis requires a multidimensional approach supported by structured algorithms and robust pharmacovigilance to identify evolving drug-associated patterns.

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Zavaleta‐Monestel et al. (2026) studied this question.

synapsesocial.com/papers/696b26d7d2a12237a934a0b5https://doi.org/10.3390/dermato6010003
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