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Muir-Torre Syndrome: The Importance of a Detailed Family History.
Burris, Christopher K H; Rodriguez, Maria E; Raven, Meisha L; Reddy, Devasis N; Xu, Yaohui G; Wiggs, Janey L; Potter, Heather D; Albert, Daniel M.
Afiliação
  • Burris CKH; Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wisconsin, USA.
  • Rodriguez ME; Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wisconsin, USA.
  • Raven ML; Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wisconsin, USA.
  • Reddy DN; Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wisconsin, USA.
  • Xu YG; Department of Dermatology, University of Wisconsin, Madison, Wisconsin, USA.
  • Wiggs JL; Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts, USA.
  • Potter HD; Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wisconsin, USA.
  • Albert DM; Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA.
Case Rep Ophthalmol ; 10(2): 180-185, 2019.
Article em En | MEDLINE | ID: mdl-31692600
ABSTRACT
Muir-Torre syndrome, a variant of Lynch syndrome or hereditary nonpolyposis colorectal cancer, is an autosomal dominant disease characterized by skin neoplasms (sebaceous or keratoacanthomas) and visceral malignancies. Due to the rarity of the syndrome there are no firm guidelines on how and when to test patients with its typical skin lesions. We describe a case that highlights the importance of a detailed family history.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article