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Childhood hypopigmented mycosis fungoides: a commonly delayed diagnosis

dc.contributor.authorGameiro, A
dc.contributor.authorGouveia, M
dc.contributor.authorTellechea, O
dc.contributor.authorMoreno, A
dc.date.accessioned2016-12-12T15:21:08Z
dc.date.available2016-12-12T15:21:08Z
dc.date.issued2014-12-23
dc.description.abstractPrimary cutaneous lymphomas (PCLs) are exceedingly rare in children and adolescents, with mycosis fungoides (MF) being the most frequent PCL diagnosed in childhood. There are numerous unusual clinical variants of MF, including the hypopigmented type form (HMF). HMF is exceptional overall, but comparatively common among children. We present an 8-year-old boy with a 3-year history of progressive, generalised, scaly, hypopigmented round patches and few erythematous papules. He was first diagnosed with pityriasis alba (PA), and moisturisers were prescribed with no improvement. Skin biopsy showed typical features of MF, and the patient was successfully treated with narrowband ultraviolet B. HMF may simulate atopic dermatitis, PA, pityriasis lichenoides, tinea versicolour, vitiligo, postinflammatory hypopigmentation or leprosy. Therefore, persistent and unusual hypopigmented lesions should be biopsied to rule out this rare variant of MF.pt_PT
dc.identifier.citationBMJ Case Rep. 2014 Dec 23;2014. pii: bcr2014208306.pt_PT
dc.identifier.doi10.1136/bcr-2014-208306pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.4/1988
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectBiopsiapt_PT
dc.subjectCriançapt_PT
dc.subjectHipopigmentaçãopt_PT
dc.subjectPitiríase Liquenoidept_PT
dc.subjectMicose Fungoidept_PT
dc.titleChildhood hypopigmented mycosis fungoides: a commonly delayed diagnosispt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPagebcr2014208306pt_PT
oaire.citation.issuedec23 1pt_PT
oaire.citation.startPagebcr2014208306pt_PT
oaire.citation.volume2014pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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