Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case

Objective: Rare disease Background: Primary cutaneous lymphomas (PCL) are a multifaceted spectrum of cutaneous T cell lymphoma (CTCL) and cutaneous B cell lymphomas (CBCL). Mycosis fungoides (MF) is a rare subset of CTCL that primarily affects adults, and its occurrence in children is exceedingly ra...

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Published in:American Journal of Case Reports
Main Author: Rosli S.; Abd Halim H.; Md-Yasin M.; Abu Bakar N.A.
Format: Article
Language:English
Published: International Scientific Information, Inc. 2025
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85215126859&doi=10.12659%2fAJCR.945897&partnerID=40&md5=d1ffdb137720de3214fa94c143bdd3d0
id 2-s2.0-85215126859
spelling 2-s2.0-85215126859
Rosli S.; Abd Halim H.; Md-Yasin M.; Abu Bakar N.A.
Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
2025
American Journal of Case Reports
26

10.12659/AJCR.945897
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85215126859&doi=10.12659%2fAJCR.945897&partnerID=40&md5=d1ffdb137720de3214fa94c143bdd3d0
Objective: Rare disease Background: Primary cutaneous lymphomas (PCL) are a multifaceted spectrum of cutaneous T cell lymphoma (CTCL) and cutaneous B cell lymphomas (CBCL). Mycosis fungoides (MF) is a rare subset of CTCL that primarily affects adults, and its occurrence in children is exceedingly rare. Most pediatric MF manifests as hypopigmented patches resembling other benign dermatoses, causing diagnostic challenges. This report outlines a case of pediatric MF in a 7-year-old Malaysian boy. Case Report: A 7-year-old boy exhibited progressing skin lesions characterized initially by erythematous, papular rashes over the face and upper limbs, then to the whole body, becoming hypopigmented, with pruritus and scaling for 1 year. Multiple clinics treated him for eczema and pityriasis alba but he responded poorly to courses of various topical steroids and emollient treatment. Due to the refractory nature of the lesions, he was subsequently referred to a dermatology clinic, where 2 skin biopsies were performed. The first biopsy revealed epidermotropism of atypical lymphocytes, consistent with MF. Immunohistochemical analysis revealed positive CD3+ expression with slightly reduced CD4+, CD7+, and CD8+ expression, and normal CD2+ and CD5+ expression at the epidermis level. Nevertheless, due to the rarity of MF in children, a second biopsy was performed, validating the diagnosis. Conclusions: Pediatric MF is a rare and challenging diagnosis. This case report highlights the importance of close monitoring of unresolved hypopigmented lesions and increased vigilance on lesions not responding to standard treatment. Timely diagnosis with support of skin biopsy is crucial to avoid potentially serious disease progression and helps provide appropriate management leading to improved outcomes. © Am J Case Rep.
International Scientific Information, Inc.
19415923
English
Article
All Open Access; Hybrid Gold Open Access
author Rosli S.; Abd Halim H.; Md-Yasin M.; Abu Bakar N.A.
spellingShingle Rosli S.; Abd Halim H.; Md-Yasin M.; Abu Bakar N.A.
Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
author_facet Rosli S.; Abd Halim H.; Md-Yasin M.; Abu Bakar N.A.
author_sort Rosli S.; Abd Halim H.; Md-Yasin M.; Abu Bakar N.A.
title Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
title_short Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
title_full Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
title_fullStr Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
title_full_unstemmed Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
title_sort Pediatric Mycosis Fungoides Mimicking Benign Dermatoses: A Report of a Rare Case
publishDate 2025
container_title American Journal of Case Reports
container_volume 26
container_issue
doi_str_mv 10.12659/AJCR.945897
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85215126859&doi=10.12659%2fAJCR.945897&partnerID=40&md5=d1ffdb137720de3214fa94c143bdd3d0
description Objective: Rare disease Background: Primary cutaneous lymphomas (PCL) are a multifaceted spectrum of cutaneous T cell lymphoma (CTCL) and cutaneous B cell lymphomas (CBCL). Mycosis fungoides (MF) is a rare subset of CTCL that primarily affects adults, and its occurrence in children is exceedingly rare. Most pediatric MF manifests as hypopigmented patches resembling other benign dermatoses, causing diagnostic challenges. This report outlines a case of pediatric MF in a 7-year-old Malaysian boy. Case Report: A 7-year-old boy exhibited progressing skin lesions characterized initially by erythematous, papular rashes over the face and upper limbs, then to the whole body, becoming hypopigmented, with pruritus and scaling for 1 year. Multiple clinics treated him for eczema and pityriasis alba but he responded poorly to courses of various topical steroids and emollient treatment. Due to the refractory nature of the lesions, he was subsequently referred to a dermatology clinic, where 2 skin biopsies were performed. The first biopsy revealed epidermotropism of atypical lymphocytes, consistent with MF. Immunohistochemical analysis revealed positive CD3+ expression with slightly reduced CD4+, CD7+, and CD8+ expression, and normal CD2+ and CD5+ expression at the epidermis level. Nevertheless, due to the rarity of MF in children, a second biopsy was performed, validating the diagnosis. Conclusions: Pediatric MF is a rare and challenging diagnosis. This case report highlights the importance of close monitoring of unresolved hypopigmented lesions and increased vigilance on lesions not responding to standard treatment. Timely diagnosis with support of skin biopsy is crucial to avoid potentially serious disease progression and helps provide appropriate management leading to improved outcomes. © Am J Case Rep.
publisher International Scientific Information, Inc.
issn 19415923
language English
format Article
accesstype All Open Access; Hybrid Gold Open Access
record_format scopus
collection Scopus
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