Urticarial mycosis fungoides: A distinctive presentation with blood involvement and a peculiar immunophenotype

Author:

Torre‐Castro Juan1ORCID,Postigo Concepción2ORCID,Machan Salma1ORCID,Jo‐Velasco Margarita Estela3,Díaz de la Pinta Javier3,Rodríguez‐Peralto Jose Luis4,Córdoba Raúl5,Requena Luis1ORCID,Rodríguez‐Pinilla Socorro María3

Affiliation:

1. Dermatology Department Hospital Universitario Fundación Jiménez Díaz, Universidad Autónoma Madrid Spain

2. Dermatology Department Hospital Universitario 12 de Octubre, Universidad Complutense Madrid Spain

3. Pathology Department Hospital Universitario Fundación Jiménez Díaz, Universidad Autónoma Madrid Spain

4. Pathology Department Hospital Universitario 12 de Octubre, Universidad Complutense Madrid Spain

5. Haematology Department Hospital Universitario Fundación Jiménez Díaz, Universidad Autónoma Madrid Spain

Abstract

AbstractMycosis fungoides (MF) has been widely reported to mimick a considerable number of different dermatoses, including scarring alopecia, bullous dermatoses or cysts, and comedones. In atypical presentations, histopathology is essential for the diagnosis. We present two cases of MF with clinical urticarial lesions and a striking blood involvement that responded to mogamulizumab treatment. Histopathologically, both cases had classic MF features and shared a peculiar immunophenotype, with positivity for CD25 and FOXP3. Differential diagnoses included urticarial lymphomatoid drug reactions and other lymphomas, like T‐cell prolymphocytic leukemia, atypical Sézary syndrome, or adult T‐cell lymphocytic leukemia. A low suspicion threshold is necessary for the diagnosis of atypical presentations of MF.

Publisher

Wiley

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