Indian Journal of Dermatology, Venereology and Leprology Medknow Publications on behalf of The Indian Association of Dermatologists, Venereologists and Leprologists (IADVL) ISSN: 0378-6323 EISSN: 0973-3922 Vol. 71, Num. 4, 2005, pp. 287-288

Indian Journal of Dermatology, Venereology and Leprology, Vol. 71, No. 4, July-August, 2005, pp. 287-288

Letter To Editor

Lichenoid eruption due to imatinib

Prabhash K., Doval D.C.

Medical Oncology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi

Correspondence Address: B7/99, Sector -4, Rohini, New Delhi, kp_prabhash@rediffmail.com

Code Number: dv05095

Sir,

Imatinib mesylate is a tyrosine kinase inhibitor. It inhibits tyrosine kinases of bcr-abl, c-Kit and platelet derived growth factor receptors (PDGFRs). This drug has revolutionized the treatment of chronic myeloid leukemia (CML) and has been recently approved as first line treatment in CML patients. Most patients receiving imatinib experience hematological and non-hematological side effects. The common non-hematological side effects are nausea, musculoskeletal pain, superficial edema, skin rashes and muscular cramps. Skin changes are the most common non-hematological adverse effects.[1] The prevalence and their relationship with the dose suggests that they are due to the direct pharmacological effect of imatinib.[2] There are three reports of a lichenoid skin eruption due to imatinib. [6],[7],[8]

A 50-year-old man presented with weakness and fatigue in November 2002. He had hepatomegaly of 4 cm and splenomegaly of 2 cm. Bone marrow aspiration was suggestive of chronic myeloproliferative disorder. Leukocyte alkaline phosphatase score was zero. His cytogenetic study was positive for Philadelphia chromosome positive. He received hydroxyurea and interferon 5 MIU/day, but there was no hematological remission and cytogenetically there was no response. He was started on imatinib 400 mg/day in May 2003. He achieved complete hematological response within two months. The cytogenetic response was partial at six months and complete at 12 months.

Six months after imatinib was started, he noticed hyper-pigmented skin lesions on the eyelids [Figure - 1], which slowly spread to involve the neck, chest, and limbs. The lesions were maculopapular, brownish black in color and non-pruritic. He refused a skin biopsy of the pigmented lesions. The patient was continued on imatinib and is doing well.

The common cutaneous adverse effects of imatinib are superficial skin edema, rashes, hypopigmentation and pruritus.[1] Rarely does it lead to severe epidermal necrolysis, acute generalized exanthematous pustulosis, hyperpigmentation or a lichenoid eruption.[3],[4],[5],[6] Reports of pigmentary changes due to imatinib are from ethnically pigmented patients, with 40.9% having hypopigmentation.[3] The molecular mechanism for the skin changes is not clear. In one report, all seven patients having depigmentation had a skin rash, suggesting a common etiology, but in another report, only 5.4% patients of patients with pigmentary changes had a skin rashe, indicating a complex molecular interaction.[2],[3]

Two of the three reported cases of lichenoid eruption due to imatinib had involvement of the buccal mucosa, and one had skin involvement. [6],[7],[8] The eruption started 12 weeks after imatinib was first administered in two patients, and after eight weeks in the third. Our patient developed a skin eruption six months after imatinib was started. This case illustrates that a lichenoid eruption can occur in patients receiving imatinib. The eruption may be mild or extensive. The mild form may not need discontinuation of imatinib as in our patients. If it is extensive, then temporary discontinuation might be needed.

REFERENCES

Copyright 2005 - Indian Journal of Dermatology, Venereology and Leprology

The following images related to this document are available:

Photo images