Muir-Torre Syndrome: The Importance of a Detailed Family History

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...

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Veröffentlicht in:Case Reports in Ophthalmology 2019-05, Vol.10 (2), p.180-185
Hauptverfasser: 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.
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Sprache:eng
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Zusammenfassung: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.
ISSN:1663-2699
1663-2699
DOI:10.1159/000500662