Mycosis fungoides-like reaction in a patient treated with Gleevec
- 1 April 2003
- journal article
- case report
- Published by Wiley in Journal of Cutaneous Pathology
- Vol. 30 (4), 279-281
- https://doi.org/10.1046/j.0303-6987.2003.053.x
Abstract
Gleevec trade mark is a protein tyrosine kinase inhibitor used in the treatment of chronic myelogenous leukemia and gastrointestinal stromal tumor. Currently, Gleevec is also being used in protocols for treatment of other malignancies such as melanoma. A few, non-descript cutaneous eruptions have been reported in patients receiving Gleevec. A patient with a gastrointestinal stromal tumor developed a centripetal, slightly pruritic, predominantly macular eruption. Histologically, there was a superficial and mid-perivascular cellular infiltrate of hyperchromatic, large lymphocytes with focal epidermotropism, thus resembling mycosis fungoides. The infiltrate was composed predominantly of T cells (CD3), with a 1:1 CD4:CD8 ratio, therefore consistent with a reactive process, i.e. a drug reaction induced by Gleevec. Gleevec should be considered in the differential diagnosis of pseudolymphoma drug eruptions.Keywords
This publication has 7 references indexed in Scilit:
- Acute Generalized Exanthematous Pustulosis Associated with STI571 in a Patient with Chronic Myeloid LeukemiaDermatology, 2001
- Researchers optimistic about sea change in cancer treatment.JAMA, 2001
- Effect of the Tyrosine Kinase Inhibitor STI571 in a Patient with a Metastatic Gastrointestinal Stromal TumorNew England Journal of Medicine, 2001
- Efficacy and Safety of a Specific Inhibitor of the BCR-ABL Tyrosine Kinase in Chronic Myeloid LeukemiaNew England Journal of Medicine, 2001
- Quantitation of intraepidermal T‐cell subsets in formalin‐fixed, paraffin‐embedded tissue helps in the diagnosis of mycosis fungoidesJournal of Cutaneous Pathology, 1999
- Mycosis fungoides-like lesions associated with phenytoin therapyArchives of Dermatology, 1985
- Pseudolymphoma with mycosis fungoides manifestations, hyperresponsiveness to diphenylhydantoin, and lymphocyte disregulationCancer, 1982