Evidence map›Paper›PMID 42771558›Full record

ArticleRevista medica del Instituto Mexicano del Seguro Social2026

Mycosis fungoides in a Mexican pediatric series: Clinical, immunophenotypic, and therapeutic features.

Juan Alberto Godínez-Chaparro, Armando Cortes-Hernández

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Article in Revista medica del Instituto Mexicano del Seguro Social, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Juan Alberto Godínez-ChaparroInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Hospital General "Dr. Gaudencio González Garza", Servicio de Dermatología Pediátrica. Ciudad de México, México.ORCID 0000-0001-8618-7264
Armando Cortes-HernándezInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Hospital General "Dr. Gaudencio González Garza", Servicio de Dermatología Pediátrica. Ciudad de México, México.ORCID 0009-0001-7970-0282

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Mycosis fungoides (MF) is a primary cutaneous lymphoma that in pediatric patients is frequently misdiagnosed as a benign dermatosis. Studies in Mexican children are limited. Objective: To describe the clinical, immunophenotypic, and therapeutic characteristics of MF in a Mexican pediatric series. Material and methods: It was conducted a cross-sectional study between 2017-2025 at a hospital in Mexico City, which included 17 pediatric patients younger than 18 years of both sexes with a diagnosis of MF. Results: They were 13 males and 4 females, with a mean age at diagnosis of 11.9 ± 2.8 years and a median disease duration of 3 years; 52.9% of patients were referred with a diagnosis of atopic dermatitis. The most frequent clinical variant was hypopigmented (64.7%). All cases were classified as stage IB. Diagnosis required a median of 2 biopsies, with delays of up to 12 months (range 3-24). All cases showed epidermotropism with CD3 and CD4 positivity (100%), and 88.2% showed CD8 positivity. All patients received topical corticosteroids; 3 received phototherapy, 3 methotrexate, and 3 photopheresis. The classic form of MF was associated with the presence of erythematous patches and erythematous scaly plaques, as well as, in some cases, with the use of methotrexate and phototherapy. Conclusions: Pediatric MF poses a diagnostic challenge due to its clinical similarity to common dermatoses. Although prognosis is generally favorable, its recurrence requires prolonged follow-up.

Indexed as

Mycosis FungoidesSkin NeoplasmsAdolescentChildCross-Sectional StudiesFemaleHumansImmunophenotypingMaleMexicoLinfoma Cutáneo de Células TLymphoma, T Cell, CutaneousMexicoMéxicoMicosis FungoideMycosis FungoidesPediatríaPediatrics

Identifiers

PMID42771558
PMCPMC13610903

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