PubMed ID: 31692600
Author(s): Burris CKH, Rodriguez ME, Raven ML, Reddy DN, Xu YG, Wiggs JL, Potter HD, Albert DM. Muir-Torre syndrome: the importance of a detailed family history. Case Rep Ophthalmol. 2019 May 23;10(2):180-185. doi: 10.1159/000500662. eCollection 2019 May-Aug. PMID 31692600
Journal: Case Reports In Ophthalmology, Volume 10, Issue 2, 2019
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.
Copyright © 2019 by S. Karger AG, Basel.