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

被引：4

作者：

Burris, Christopher K. H. ^{[1
]}

Rodriguez, Maria E. ^{[1
]}

Raven, Meisha L. ^{[1
]}

Reddy, Devasis N. ^{[1
]}

Xu, Yaohui G. ^{[2
]}

Wiggs, Janey L. ^{[3
]}

Potter, Heather D. ^{[1
]}

Albert, Daniel M. ^{[4
]}

机构：

[1] Univ Wisconsin, Dept Ophthalmol & Visual Sci, Madison, WI USA

[2] Univ Wisconsin, Dept Dermatol, Madison, WI USA

[3] Harvard Med Sch, Massachusetts Eye & Ear Infirm, Boston, MA 02115 USA

[4] Oregon Hlth & Sci Univ, Casey Eye Inst, Portland, OR 97201 USA

来源：

CASE REPORTS IN OPHTHALMOLOGY | 2019年 / 10卷 / 02期

基金：

美国国家卫生研究院;

关键词：

Lynch syndrome; Sebaceous carcinoma; Muir-Torre syndrome; MICROSATELLITE INSTABILITY; CANCER; IMMUNOHISTOCHEMISTRY; IDENTIFICATION; TUMORS;

D O I：

10.1159/000500662

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

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. (C) 2019 The Author(s) Published by S. Karger AG, Basel

引用

页码：180 / 185

页数：6

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