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Evidence Levels: A Double-blind study B Clinical trial ≥ 20 subjects C Clinical trial < 20 subjects D Series ≥ 5 subjects E Anecdotal case reports
Acute generalized exanthematous pustulosis (AGEP) is characterized by the acute onset of numerous small, non-follicular, sterile pustules arising on a diffuse erythematous base in a febrile patient with an accompanying blood neutrophilia. Most cases occur in the context of drug ingestion (commonly within 24 hours). Rapid resolution after drug withdrawal is the usual outcome.
Treatment of AGEP involves establishing the correct diagnosis coupled with the withdrawal of any implicated medication ( Table 8.1 ). Pustular psoriasis is its main differential diagnosis. A comprehensive drug history and a personal or family history of psoriasis are therefore required.
Drugs |
Antibiotics |
Penicillins: amoxicillin, ampicillin, bacampicillin, pipemidic acid, piperacillin, propicillin, tazobactam, meropenem Macrolides: azithromycin, erythromycin Quinolones: ciprofloxacin, norfloxacin, ofloxacin Tetracyclines: doxycycline, minocycline Cephalosporins: cefaclor, cefazolin, cefuroxime, cephalexin, cephradine Aminoglycosides: gentamicin, isepamicin sulfate, streptomycin Other antibiotics Chloramphenicol, clindamycin, cotrimoxazole, imipenem/cilastatin, lincomycin, metronidazole, nifuroxazide, sulfamethoxazole, teicoplanin, vancomycin, daptomycin, telavancin |
NSAIDs |
Celecoxib, etoricoxib, ibuprofen, naproxen, nimesulide, valdecoxib |
ACE inhibitors |
Captopril, enalapril |
Calcium channel blockers |
Nifedipine, nimodipine, diltiazem |
Anticonvulsants |
Carbamazepine, phenobarbital, phenytoin |
Analgesia (opioid/non-opioid) |
Acetaminophen, paracetamol, morphine, codeine, dextropropoxyphene |
Antiplatelets |
Aspirin, ticlopidine, clopidogrel |
Benzodiazepines |
Clobazam, nitrazepam, tetrazepam |
Antimalarials |
Chloroquine, hydroxychloroquine, proguanil, pyrimethamine |
Antipsychotics |
Clozapine, chlorpromazine |
Antifungals |
Amphotericin, fluconazole, itraconazole, nystatin, terbinafine |
Antivirals |
Lamivudine, lopinavir, ritonavir, zidovudine |
Antituberculosis drugs |
Isoniazid, rifampicin |
Proton pump inhibitors |
Lansoprazole, omeprazole |
Immunosuppressants |
Azathioprine |
Antidepressants |
Amoxapine, sertraline |
Antihistamines |
Clemastine, hydroxyzine |
Beta agonists and antagonists |
Buphenine, fenoterol, nadolol |
H 2 -receptor antagonists |
Cimetidine, famotidine, ranitidine |
Cholesterol-lowering medications |
Simvastatin, pitavastatin, fenofibrate |
Corticosteroids |
Dexamethasone, methylprednisolone, prednisolone |
Diuretics |
Furosemide, hydrochlorothiazide |
Antineoplastic drugs |
Gefitinib, imatinib, vemurafenib |
Other drugs |
Acetazolamide, allopurinol, bamifylline, bleomycin, bupropion hydrochloride, cadralazine, carbimazole, carbutamide, cytarabine, dalteparin, disulfiram, eperisone hydrochloride, eprazinone, fluindione, icodextrin, interferon, metamizole, pentoxifylline, piperazine, propafenone, alprostadil, progestogens, pseudoephedrine, psoralen + UVA, quinidine, ranolazine, sulbutiamine, senna, sulfasalazine, terazosin, thalidomide |
Other substances |
Chromium picolinate Diphenyl sulfone Contrast agents iohexol and iopamidol Mercury Pneumococcal vaccine Essential oil Andrographis paniculata |
Intraepidermal or subcorneal pustules in conjunction with a leukocytoclastic vasculitis, focal necrosis of keratinocytes, marked edema of the papillary dermis, and an infiltrate of eosinophils are histologic features that help distinguish AGEP from pustular psoriasis; biopsy is thus an integral facet of management.
Differentiation of AGEP from other inflammatory, toxic, or infectious conditions, such as Sneddon–Wilkinson disease (subcorneal pustular dermatosis) or, in severe cases, toxic epidermal necrolysis, is often readily apparent both clinically and histologically. The clinician should, however, be aware that erythema multiform–like targetoid lesions, mucous membrane involvement, facial edema, purpura, and vesiculobullous lesions have all been documented in the context of AGEP.
Antibiotics (primarily penicillin or macrolide based) are the most frequently implicated medications. Numerous case reports have cited various other causative agents, including calcium channel blockers, non-steroidal antiinflammatory drugs (NSAIDs), angiotensin-converting enzyme (ACE) inhibitors, and anticonvulsants ( Table 8.1 ). Acute enterovirus infection, mycoplasma pneumonia, cytomegalovirus, parvovirus B19, spider bites, Chinese herbal compounds (ginkgo biloba), contrast media, and mercury exposure have also been reported as possible causes.
There is no specific therapy for AGEP. A skin swab establishes the sterile nature of the pustules, and drug withdrawal, if feasible, results in rapid spontaneous resolution. Supportive therapy is all that is required. A superficial desquamation often occurs during this time and may be treated with simple emollients . Several case reports cite the use of patch testing to confirm the causative medication. Recalcitrant cases have benefited from oral prednisolone , ciclosporin , and secukinumab .
Sidoroff A, Dunant A, Viboud C. Br J Dermatol 2007; 157: 6.
A multinational case-control study (97 cases of AGEP and 1009 controls) that assessed the risk for different drugs causing severe cutaneous adverse reactions.
The most frequently implicated drugs were pristinamycin (a macrolide marketed in France), ampicillin/amoxicillin, quinolones, (hydroxy)chloroquine, anti-infective sulfonamides, terbinafine, and diltiazem. Infections and a personal or family history of psoriasis were not deemed to be significant risk factors for developing AGEP. Of note, the median treatment duration was 1 day for antibiotics and 11 days for all other associated drugs.
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