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Birt-Hogg-Dubé Syndrome

dc.contributor.authorLencastre, A
dc.contributor.authorPonte, P
dc.contributor.authorApetato, M
dc.contributor.authorNunes, L
dc.contributor.authorLestre, S
dc.date.accessioned2014-01-23T10:13:58Z
dc.date.available2014-01-23T10:13:58Z
dc.date.issued2013
dc.description.abstractA 45-year-old woman with a history of renal carcinoma was observed for facial, cervical and truncal flesh-colored papules. Relatives had similar skin findings and a brother had repeated episodes of pneumothorax. The computerized tomography scan revealed multiple cysts on both lungs. A skin biopsy revealed a perifollicular fibroma. The clinical diagnosis of Birt-Hogg-Dubé syndrome (BHDS) was corroborated by identification of a novel frameshift c.573delGAinsT (p.G191fsX31) mutation in heterozygosity on exon 6 of the folliculin gene. The presence of multiple and typical benign hair follicle tumors highlights the role of the dermatologist in the diagnosis of this rare genodermatosis that is associated with an increased risk of renal cell cancer and pulmonary cysts, warranting personal and familial follow-up and counseling.por
dc.identifier.citationAn Bras Dermatol. 2013;88(6 Suppl 1):203-5por
dc.identifier.urihttp://hdl.handle.net/10400.17/1629
dc.language.isoengpor
dc.peerreviewedYes
dc.publisherSociedade Brasileira de Dermatologiapor
dc.subjectSíndrome de Birt-Hogg-Dubépor
dc.subjectMutação da Fase de Leiturapor
dc.subjectFolículo Pilosopor
dc.subjectHDE GENpor
dc.subjectHSAC DERpor
dc.titleBirt-Hogg-Dubé Syndromepor
dc.title.alternativeSíndrome de Birt-Hogg-Dubépor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage205por
oaire.citation.startPage203por
oaire.citation.volume88por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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