Low-dose methotrexate-induced skin toxicity: Keratinocyte dystrophy as a histologic marker.

J Am Acad Dermatol

Département de Dermatologie, Assistance Publique-Hôpitaux de Paris (AP-HP) Hôpitaux universitaires Henri Mondor, Créteil, France; Inserm, Centre d'Investigation Clinique 1430, Créteil, France; Equipe d'Accueil (EA) EpiDermE, Université Paris-Est Créteil, Créteil, France.

Published: September 2015

Background: Skin toxicity during low-dose methotrexate therapy is rare, ill described, and reported to have nonspecific histologic characteristics. Thus, misdiagnosis is common in patients with mucosal ulcers and/or skin erosions related to low-dose methotrexate.

Objective: We sought to describe the features of skin toxicity induced by low-dose methotrexate.

Methods: We evaluated the clinical and histologic features in 5 patients who experienced skin toxicity induced by low-dose methotrexate between 2011 and 2013.

Results: All 5 patients had acute mucosal ulcers, 4 had moderately abnormal blood cell counts, and 3 had skin erosions. In 3 patients, methotrexate dosage or dosing-schedule errors were identified. No other contributing factors (eg, renal dysfunction or interacting drugs) were identified. Mucocutaneous biopsy specimens consistently showed multiple dystrophic keratinocytes.

Limitations: We studied only 5 patients and obtained no sensitivity or specificity data on the diagnostic value of keratinocyte dystrophy.

Conclusion: Keratinocyte dystrophy may help to diagnose skin toxicity of low-dose methotrexate, even in the absence of known risk factors or methotrexate administration errors. Studies of the diagnostic performance of this histologic sign are needed.

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Source
http://dx.doi.org/10.1016/j.jaad.2015.06.015DOI Listing

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