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Cutaneous Leiomyomatosis in a Mother and Daughter

dc.contributor.authorLencastre, A
dc.contributor.authorCabete, J
dc.contributor.authorGonçalves, R
dc.contributor.authorJoão, A
dc.contributor.authorFidalgo, A
dc.date.accessioned2014-05-23T16:16:02Z
dc.date.available2014-05-23T16:16:02Z
dc.date.issued2013
dc.description.abstractA 34-year-old woman with no known medical history was evaluated for multiple painful brown nodules and papules on the anterior aspect of the trunk. She mentioned a history of similar cutaneous findings on her mother. Biopsies of three lesions revealed piloleiomyomata. Renal and adrenal ultrasound revealed an isolated simple cortical cyst, and pelvic and endovaginal ultrasound revealed two uterine myomata. The clinical diagnosis of hereditary leiomyomatosis and renal cell cancer was corroborated by the identification of a heterozygous variant on exon 5 of the fumarate hydratase gene (c.578C>T p.T193I). Identification of the tumor piloleiomyoma should alert the dermatologist to this rare genodermatosis, which is associated with an increased risk of renal cell tumors, demanding multidisciplinary follow-up, and personal and family counseling.por
dc.identifier.citationAn Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):124-7por
dc.identifier.urihttp://hdl.handle.net/10400.17/1805
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherScielopor
dc.subjectHSAC DERpor
dc.subjectBiópsiapor
dc.subjectCarcinoma de Células Renaispor
dc.subjectNeoplasias do Úteropor
dc.subjectFumarato Hidratasepor
dc.subjectPredisposição Genética para a Doençapor
dc.subjectNeoplasias Renaispor
dc.subjectLeiomiomatosepor
dc.subjectPelepor
dc.subjectNeoplasias da Pelepor
dc.subjectHDE GEN
dc.titleCutaneous Leiomyomatosis in a Mother and Daughterpor
dc.title.alternativeLeiomiomatose Cutânea em Mãe e Filhapor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage127por
oaire.citation.startPage124por
oaire.citation.titleAnais Brasileiros de Dermatologiapor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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