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Childhood Hypopigmented Mycosis Fungoides: A Rare Diagnosis.
Patraquim, Cláudia; Gomes, Maria Miguel; Garcez, Carla; Leite, Filipa; Oliva, Tereza; Santos, António; Pinto, Armando.
Afiliação
  • Patraquim C; Pediatrics Department, Hospital de Braga, Sete Fontes, São Victor, 4710-243 Braga, Portugal.
  • Gomes MM; Pediatrics Department, Hospital de Braga, Sete Fontes, São Victor, 4710-243 Braga, Portugal.
  • Garcez C; Pediatrics Department, Hospital de Braga, Sete Fontes, São Victor, 4710-243 Braga, Portugal.
  • Leite F; Pediatrics Department, Portuguese Oncology Institute of Porto Francisco Gentil, 4200-072 Porto, Portugal.
  • Oliva T; Pediatrics Department, Portuguese Oncology Institute of Porto Francisco Gentil, 4200-072 Porto, Portugal.
  • Santos A; Dermatology Department, Portuguese Oncology Institute of Porto Francisco Gentil, 4200-072 Porto, Portugal.
  • Pinto A; Pediatrics Department, Portuguese Oncology Institute of Porto Francisco Gentil, 4200-072 Porto, Portugal.
Case Rep Pediatr ; 2016: 8564389, 2016.
Article em En | MEDLINE | ID: mdl-28025633
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article