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E-IJD CASE REPORT |
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Year : 2016 | Volume
: 61
| Issue : 2 | Page : 235 |
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Acute generalized exanthematous pustulosis induced by fexofenadine |
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Tanvi Gupta, Vijay K Garg, Rashmi Sarkar, Anjali Madan
Department of Dermatology and Venereology, Maulana Azad Medical College and Associated Hospitals, New Delhi, India
Date of Web Publication | 1-Mar-2016 |
Correspondence Address: Rashmi Sarkar Department of Dermatology and Venereology, Maulana Azad Medical College and Associated Hospitals, Bahadur Shah Zafar Marg, New Delhi - 110 002 India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0019-5154.177787
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Abstract | | |
Acute generalized exanthematous pustulosis (AGEP) is a skin eruption, frequently drug induced and characterized by the acute development of multiple sterile minute pustules on an erythematous base. There is no case of fexofenadine-induced AGEP in literature (PubMed search). A 40-year-old female presented to us with fever and sudden onset development of multiple discrete to coalescent 1–2 mm nonfollicular pustules on an erythematous base present mainly on her trunk and upper extremities for past 2 days. She had a history of use of fexofenadine 180 mg OD for rhinitis for 2 days. Gram's stain showed no organism and pus culture showed no growth. Histopathological examination revealed subcorneal pustules with epidermal spongiosis. Scattered neutrophils and eosinophils were noted in the dermis. During this period, she took fexofenadine 180 mg unknowingly once following which she developed similar episode within 24–48 h. After withdrawal of the drug, the lesions subsided with scaling in 8–10 days. To the best of our knowledge, this is the first reported case of AGEP induced by fexofenadine. Recognition of such a rare entity is important given the frequent usage of fexofenadine for allergic disorders.
Keywords: Acute generalized exanthematous pustulosis, drug rash, fexofenadine
How to cite this article: Gupta T, Garg VK, Sarkar R, Madan A. Acute generalized exanthematous pustulosis induced by fexofenadine. Indian J Dermatol 2016;61:235 |
How to cite this URL: Gupta T, Garg VK, Sarkar R, Madan A. Acute generalized exanthematous pustulosis induced by fexofenadine. Indian J Dermatol [serial online] 2016 [cited 2023 Sep 25];61:235. Available from: https://www.e-ijd.org/text.asp?2016/61/2/235/177787 |
What was known?
Acute generalized exanthematous pustulosis is an acute skin eruption frequently drug induced.
Introduction | |  |
Acute generalized exanthematous pustulosis (AGEP) was first described by Baker and Ryan in 1968 as exanthematic pustular psoriasis in 5 patients with no history of psoriasis and was drug-induced.[1] The term AGEP was first used by Beylot et al in 1980.[2] It is a self-limiting disease characterized by acute onset of lesions after intake of the drug with disappearance of lesions within 15 days after discontinuation of the drug; the presence of numerous nonfollicular sterile pustules, <5 mm on an erythematous background, fever >38°C, and peripheral blood leukocytosis (neutrophilia) and a histopathological finding of subcorneal pustules, epidermal spongiosis, and dermal collection of neutrophils and eosinophils ± vasculitis and focal keratinocyte necrosis.[3]
Ninety percent cases of AGEP are attributed to drugs (mainly antibiotics, such as amino-penicillin and macrolides). There are reports of AGEP caused by various drugs in literature; however, this is the first reported case of fexofenadine-induced AGEP.
Case Report | |  |
A 40-year-old female presented to our outpatient department with fever >38°C and sudden onset development of multiple discrete to coalescent 1–2 mm nonfollicular pustules on an erythematous base present mainly on her trunk and upper extremities for the past 2 days [Figure 1]. She gave a history of intake of fexofenadine 180 mg OD for rhinitis. She developed the lesions after 2 days of the start of treatment. There were no systemic complaints and no family history. Mucosa and nails were uninvolved. | Figure 1: 1–2 mm nonfollicular pustules on an erythematous background on the trunk
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On investigating the patient, hemogram revealed leukocytosis with neutrophilia. Gram's stain showed no organism and pus culture showed no growth. The histopathology report revealed subcorneal pustules with epidermal spongiosis along with scattered neutrophils and eosinophils in the dermis [Figure 2]. During this period, she took fexofenadine 180 mg once unknowingly following which she developed similar episode within 24–48 h. After withdrawal of the drug, the lesions subsided with scaling in 8–10 days. A diagnosis of AGEP caused by fexofenadine was made on the basis of clinical features, histopathology, and an accidental oral provocation test. The score on Naranjo adverse drug reaction probability scale was 9. | Figure 2: H and E section of the biopsy specimen showing subcorneal pustules with neutrophils and epidermal spongiosis (×400)
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Discussion | |  |
Drugs known to cause AGEP are β-lactam antibiotics, macrolides, doxycycline, terbinafine, nifedipine, carbamazepine, and others.[3]
Fexofenadine is an active metabolite of terfenadine and is a second generation antihistamine derived from piperidines. The most common adverse reactions related to fexofenadine have been a headache, dizziness, daytime drowsiness, nausea, and it has been very rarely reported to cause hypersensitivity.[4] AGEP developing as a side-effect of antihistamines such as cetirizine [5] and hydroxyzine [6] has been reported in the past but not to fexofenadine.
The exact mechanism of fexofenadine-induced AGEP in our patient could not be elucidated.
There are four case reports of fexofenadine-induced urticaria in literature.[7],[8],[9] One of the possible mechanisms of urticaria is it being a Type IV hypersensitivity reaction.[10] AGEP is also a Type IV delayed hypersensitivity response,[10] thus, fexofenadine might have induced AGEP by the same mechanism as in the case of urticaria.
Our patient demonstrated clear clinical and histopathological findings of AGEP induced by fexofenadine. The condition resolved quickly and completely after discontinuation of the drug.
We are reporting this case as, to the best of our knowledge, there is no case of fexofenadine- induced AGEP in literature until date. Knowledge of such a rare adverse effect is important as fexofenadine is a commonly prescribed drug by dermatologists, otorhinolaryngologists, and general practitioners for various indications.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References | |  |
1. | Baker H, Ryan TJ. Generalized pustular psoriasis. A clinical and epidemiological study of 104 cases. Br J Dermatol 1968;80:771-93.  [ PUBMED] |
2. | Beylot C, Bioulac P, Doutre MS. Acute generalized exanthematic pustuloses (four cases). Ann Dermatol Venereol 1980;107:37-48.  [ PUBMED] |
3. | Roujeau JC, Bioulac-Sage P, Bourseau C, Guillaume JC, Bernard P, Lok C, et al. Acute generalized exanthematous pustulosis. Analysis of 63 cases. Arch Dermatol 1991;127:1333-8. |
4. | Markham A, Wagstaff AJ. Fexofenadine. Drugs 1998;55:269-74. |
5. | Badawi AH, Tefft K, Fraga GR, Liu DY. Cetirizine-induced acute generalized exanthematous pustulosis: A serious reaction to a commonly used drug. Dermatol Online J 2014;20:22613. |
6. | Kumar SL, Rai R. Hydroxyzine-induced acute generalized exanthematous pustulosis: An uncommon side effect of a common drug. Indian J Dermatol 2011;56:447-8.  [ PUBMED] |
7. | Lee SW, Byun JY, Choi YW, Myung KB, Choi HY. Fexofenadine-induced urticaria. Ann Dermatol 2011;23 Suppl 3:S329-32. |
8. | Demoly P, Messaad D, Benahmed S, Sahla H, Bousquet J. Hypersensitivity to H1-antihistamines. Allergy 2000;55:679-80. |
9. | González de Olano D, Roán Roán J, de la Hoz Caballer B, Cuevas Agustín M, Hinojosa Macías M. Urticaria induced by antihistamines. J Investig Allergol Clin Immunol 2006;16:144-6. |
10. | Pichler WJ. Immune mechanism of drug hypersensitivity. Immunol Allergy Clin North Am 2004;24:373-97, v-vi. |
What is new?
Acute generalized exanthematous pustulosis induced by fexofenadine is an unknown entity, not reported so far.
[Figure 1], [Figure 2] |
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