Literature DB >> 26729964

Terbinafine induced pityriasis rosea-like eruption.

Anisha George1, Anuradha Bhatia1, Bimal Kanish1, Abhilasha Williams1.   

Abstract

Terbinafine is an allylamine antifungal agent which is widely used for the treatment of fungal infections. Cutaneous side effects have been reported in 2% of the patients on terbinafine therapy with many morphological patterns. We report a case of terbinafine induced pityriasis rosea, a very rare side effect of terbinafine. This report emphasizes the importance of counseling the patient to report immediately in the event of a cutaneous eruption.

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Keywords:  Adverse drug reaction; drug rash; pityriasis rosea; terbinafine

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Year:  2015        PMID: 26729964      PMCID: PMC4689026          DOI: 10.4103/0253-7613.169574

Source DB:  PubMed          Journal:  Indian J Pharmacol        ISSN: 0253-7613            Impact factor:   1.200


Introduction

Terbinafine is an allylamine, a lipophilic compound, used for the treatment of onychomycosis and other fungal infections. Adverse effects are reported in 10% and cutaneous reactions in 2% of patients on terbinafine therapy.[1] These include pruritus, rash, urticaria, erythema multiforme, cutaneous lupus, and psoriasis. Terbinafine induced pityriasis rosea-like eruption is not common.

Case Report

A 25-year-old male with mycologically confirmed fingernail onychomycosis, who was prescribed oral terbinafine 250 mg daily for 18 days, presented with an itchy rash on the body for 4 days. The rash started on the chest and then progressed to involve the rest of the body within 4 days [Figure 1]. There was no history of fever or preceding upper respiratory illness. He was not on any other medication simultaneously and never had a similar rash in the past. There was no history of previous drug allergy. He had taken terbinafine for 1 month for the same indication, which he discontinued 2 weeks before restarting the present course of this antifungal. There was no family history of similar illness.
Figure 1

Erythematous plaques with elevated borders and collarettes of fine scaling on the back. Most of the lesions have their long axis parallel to the lines of cleavage giving a “Christmas tree” distribution

Erythematous plaques with elevated borders and collarettes of fine scaling on the back. Most of the lesions have their long axis parallel to the lines of cleavage giving a “Christmas tree” distribution General physical examination was noncontributory. Cutaneous examination revealed scattered erythematous papules and plaques on the trunk, upper limbs, and gluteal region. Few plaques were noted to have peripheral collarettes of scaling. Erythematous tumid plaques were noted on the cheeks. There was a single erythematous papule on the penile shaft. Scalp and oral mucosa were normal. Few fingernails were dystrophic. He was clinically diagnosed to have terbinafine induced pityriasis rosea-like eruption and admitted in the dermatology ward. Investigations revealed a total leukocyte count of 5.2 × 109/L with a differential of 67% neutrophils, 30% lymphocytes, and 2% eosinophils. Liver and renal function tests were within normal limits. The Venereal disease research laboratory (VDRL) test was carried out to rule out secondary syphilis, which was negative. However, a skin biopsy was not performed. The offending drug, terbinafine, was withdrawn. The patient was given supportive management in the form of antihistamines and topical steroids. The rash began to resolve quickly, and the patient was discharged from the hospital after 4 days. The common cutaneous adverse effects associated with terbinafine therapy are urticaria, rash, and pruritus, usually occurring within a month of therapy. The other less common adverse effects are erythema multiforme, toxic epidermal necrolysis, Stevens–Johnson syndrome, erythema annulare-like eruption, fixed drug eruption, alopecia areata, flare up of dermatitis,[1] induction and exacerbation of psoriasis,[23] and subacute cutaneous lupus-like eruption.[4] Pityriasis rosea is a rare adverse effect of terbinafine therapy.[5] Pityriasis rosea is an inflammatory skin disease characterized by erythematous papulosquamous eruptions localized mainly to the trunk. Viral agents, especially human herpes virus 6 and 7, autoimmunity, drugs such as captopril, nonsteroidal anti-inflammatory drugs, barbiturates, metronidazole, isotretinoin, griseofulvin, terbinafine, and psychogenic factors have been proposed as possible etiological factors.[6] The initial lesion is larger than subsequent lesions and is called the herald patch. This herald patch is usually absent in drug induced pityriasis rosea; in our patient too, this feature was conspicuously absent. Itching was a prominent feature in our patient which is consistent with a drug reaction. Gupta et al.[5] have reported pityriasis rosea as an itchy rash beginning on the trunk after 4 weeks of regular treatment with terbinafine. The patient developed lesions after 18 days of regular treatment; however, he had been previously sensitized during the prior treatment with the drug. Secondary syphilis can a have similar cutaneous presentation but is usually asymptomatic. The patient denied a history of unprotected sexual intercourse and VDRL was negative. Pityriasiform variant of seborrhoeic dermatitis was ruled out because other seborrhoeic sites were spared, and there were no previous episodes of such eruptions. The other supportive evidence in favor of a drug-induced reaction was the improvement noted in the lesions on stopping the offending drug. Pityriasis rosea typically occurs in the spring season with a history of preceding upper respiratory infection. The patient presented in winter without any prodrome. The Naranjo causality assessment score for this case was 6, thereby suggesting probable causal association of the adverse drug reaction with terbinafine. It is recommended that all patients who receive terbinafine therapy should be counseled about the possible adverse effects and instructed to discontinue the drug and report to the physician if a cutaneous eruption develops.

Financial Support and Sponsorship

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Conflicts of Interest

There are no conflicts of interest.
  6 in total

1.  Subacute lupus erythematosus-like eruption due to terbinafine: report of three cases.

Authors:  V A Hill; J Chow; N Cowley; R A Marsden
Journal:  Br J Dermatol       Date:  2003-05       Impact factor: 9.302

Review 2.  Pityriasis rosea: an important papulosquamous disorder.

Authors:  Lenis M González; Robert Allen; Camila Krysicka Janniger; Robert A Schwartz
Journal:  Int J Dermatol       Date:  2005-09       Impact factor: 2.736

3.  Cutaneous adverse effects associated with terbinafine therapy: 10 case reports and a review of the literature.

Authors:  A K Gupta; C W Lynde; G J Lauzon; M A Mehlmauer; S W Braddock; C A Miller; J Q Del Rosso; N H Shear
Journal:  Br J Dermatol       Date:  1998-03       Impact factor: 9.302

Review 4.  Adverse drug reactions of the new oral antifungal agents--terbinafine, fluconazole, and itraconazole.

Authors:  B Amichai; M H Grunwald
Journal:  Int J Dermatol       Date:  1998-06       Impact factor: 2.736

5.  The role of terbinafine in induction and/or exacerbation of psoriasis.

Authors:  Constantinos D Verros; Efstathios Rallis
Journal:  Int J Dermatol       Date:  2012-09-24       Impact factor: 2.736

Review 6.  Terbinafine therapy may be associated with the development of psoriasis de novo or its exacerbation: four case reports and a review of drug-induced psoriasis.

Authors:  A K Gupta; R G Sibbald; S R Knowles; C W Lynde; N H Shear
Journal:  J Am Acad Dermatol       Date:  1997-05       Impact factor: 11.527

  6 in total
  4 in total

1.  CYP2C19 and 3A4 Dominate Metabolic Clearance and Bioactivation of Terbinafine Based on Computational and Experimental Approaches.

Authors:  Mary A Davis; Dustyn A Barnette; Noah R Flynn; Anirudh S Pidugu; S Joshua Swamidass; Gunnar Boysen; Grover P Miller
Journal:  Chem Res Toxicol       Date:  2019-04-10       Impact factor: 3.739

2.  Allergic Maculo-Papular Exanthema Due To Terbinafine.

Authors:  André Koch; Georgi Tchernev; Uwe Wollina
Journal:  Open Access Maced J Med Sci       Date:  2017-07-20

3.  Oral Antifungal Therapy: Emerging Culprits of Cutaneous Adverse Drug Reactions.

Authors:  Raju G Chaudhary; Santoshdev P Rathod; Ashish Jagati; Dhara Zankat; Arwinder K Brar; Bansri Mahadevia
Journal:  Indian Dermatol Online J       Date:  2019 Mar-Apr

4.  Reply: Commentary on letter to the editor from Drago et al.

Authors:  Carole Bitar; Andrea Murina
Journal:  JAAD Case Rep       Date:  2018-09-18
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