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Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis
Primary cutaneous lymphomas (PCL) are rare in pediatrics. Mycosis fungoides (MF) is the most frequent PCL diagnosed in childhood. There are various clinical variants of MF, including the hypopigmented MF (HMF). We present a 5-year-old boy with an 18-month history of progressive, generalized, nonprur...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153468/ https://www.ncbi.nlm.nih.gov/pubmed/28025633 http://dx.doi.org/10.1155/2016/8564389 |
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author | Patraquim, Cláudia Gomes, Maria Miguel Garcez, Carla Leite, Filipa Oliva, Tereza Santos, António Pinto, Armando |
author_facet | Patraquim, Cláudia Gomes, Maria Miguel Garcez, Carla Leite, Filipa Oliva, Tereza Santos, António Pinto, Armando |
author_sort | Patraquim, Cláudia |
collection | PubMed |
description | Primary cutaneous lymphomas (PCL) are rare in pediatrics. Mycosis fungoides (MF) is the most frequent PCL diagnosed in childhood. There are various clinical variants of MF, including the hypopigmented MF (HMF). We present a 5-year-old boy with an 18-month history of progressive, generalized, nonpruritic hypopigmented lesions with central lacy erythema. He had no improvement with emollients. Skin biopsy showed typical features of HMF. He was treated with topical corticosteroids and tacrolimus and narrow-band ultraviolet B (NBUVB) phototherapy, with good response. HMF may mimic multiple skin disorders. Unusual hypopigmented skin lesions should be biopsied. Though phototherapy is effective, recurrence is common. |
format | Online Article Text |
id | pubmed-5153468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-51534682016-12-26 Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis Patraquim, Cláudia Gomes, Maria Miguel Garcez, Carla Leite, Filipa Oliva, Tereza Santos, António Pinto, Armando Case Rep Pediatr Case Report Primary cutaneous lymphomas (PCL) are rare in pediatrics. Mycosis fungoides (MF) is the most frequent PCL diagnosed in childhood. There are various clinical variants of MF, including the hypopigmented MF (HMF). We present a 5-year-old boy with an 18-month history of progressive, generalized, nonpruritic hypopigmented lesions with central lacy erythema. He had no improvement with emollients. Skin biopsy showed typical features of HMF. He was treated with topical corticosteroids and tacrolimus and narrow-band ultraviolet B (NBUVB) phototherapy, with good response. HMF may mimic multiple skin disorders. Unusual hypopigmented skin lesions should be biopsied. Though phototherapy is effective, recurrence is common. Hindawi Publishing Corporation 2016 2016-11-29 /pmc/articles/PMC5153468/ /pubmed/28025633 http://dx.doi.org/10.1155/2016/8564389 Text en Copyright © 2016 Cláudia Patraquim et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Patraquim, Cláudia Gomes, Maria Miguel Garcez, Carla Leite, Filipa Oliva, Tereza Santos, António Pinto, Armando Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis |
title | Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis |
title_full | Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis |
title_fullStr | Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis |
title_full_unstemmed | Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis |
title_short | Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis |
title_sort | childhood hypopigmented mycosis fungoides: a rare diagnosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153468/ https://www.ncbi.nlm.nih.gov/pubmed/28025633 http://dx.doi.org/10.1155/2016/8564389 |
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