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Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
Life-Threatening Atypical Case of Acute Generalized Exanthematous Pustulosis
Azadeh Tajmir-Riahi1, Petra Wörl, Thomas Harrer
1Departmens of Dermatology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Abstract:
Antibiotics are known to cause severe cutaneous adverse reactions, such as the rare acute generalized exanthematous pustulosis (AGEP). Unlike Stevens-Johnson syndrome or toxic epidermal necrolysis, AGEP is rarely life-threatening. Systemic involvement is not typical, and if present usually coincides with a mild elevation of the hepatic enzymes and a decrease in renal function. Hence, AGEP is known to have a good prognosis and to be life-threatening only in elderly patients or patients with chronic diseases. Herein, we report a case of AGEP in a young healthy male leading to systemic inflammatory response syndrome and to treatment in an intensive care unit after being treated with 5 different antibiotics. Initial symptoms were not indicative for AGEP and the patient's course of disease led promptly to critical cardiorespiratory symptoms and systemic inflammatory response syndrome. We assume that the administration of the 5 different antibiotics resulted in type IV allergy as well as secondary infection with Enterococcus faecium and Staphylococcus aureus, while the underlying periodontitis also contributed to the severity of this case.
Insights
Acute generalized exanthematous pustulosis (AGEP) is a severe skin reaction to antibiotics. This case highlights a rare, severe AGEP presentation in a young, healthy male, leading to critical illness.
Area of Science:
- Dermatology
- Pharmacology
- Infectious Diseases
Background:
- Antibiotics can cause severe cutaneous adverse reactions, including acute generalized exanthematous pustulosis (AGEP).
- AGEP is typically non-life-threatening with minimal systemic involvement.
- Good prognosis is generally expected for AGEP, except in vulnerable populations.
Observation:
- A young, healthy male developed AGEP after treatment with five different antibiotics.
- Initial symptoms were atypical for AGEP, rapidly progressing to critical cardiorespiratory compromise.
- The patient developed systemic inflammatory response syndrome (SIRS) and required intensive care.
Findings:
- The severe AGEP presentation was linked to multiple antibiotic exposures.
- Type IV hypersensitivity reaction to antibiotics is suspected.
- Secondary infections with Enterococcus faecium and Staphylococcus aureus were identified.
- Underlying periodontitis may have exacerbated the condition.
Implications:
- This case underscores the potential for severe AGEP presentations even in young, healthy individuals.
- Early recognition and management of atypical AGEP are crucial.
- The interplay between antibiotic allergy, secondary infections, and underlying conditions can lead to severe outcomes.
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