Sebaceous gland tumor with a rare gene mutation within a tumor syndrome. Muir-Torre syndrome

被引：0

作者：

Voigt, E. ^{[1
]}

Sommer, F. ^{[1
]}

Geiger, K. D. ^{[2
]}

Pillunat, L. E. ^{[1
]}

机构：

[1] Univ Augenklin Dresden, D-01307 Dresden, Germany

[2] Univ Klinikum Dresden, Neuropathol Inst Pathol, Dresden, Germany

来源：

OPHTHALMOLOGE | 2014年 / 111卷 / 04期

关键词：

Hereditary nonpolyposis colorectal carcinoma; Sebaceous gland neoplasms; MSH; 6; Keratoacanthoma; Eyelid tumor; ENDOMETRIAL CANCER; MSH6; MUTATION; FAMILY;

D O I：

10.1007/s00347-013-2879-x

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

Muir-Torre syndrome is a rare autosomal dominant subtype of hereditary nonpolyposis colorectal carcinoma and is characterized by the simultaneous occurrence of sebaceous gland neoplasms with visceral and urogenital malignancies. This article describes the case of a 72-year-old patient who was referred to our clinic for removal of an upper eyelid tumor, showing the course from the clinical findings to the rare diagnosis of Muir-Torre syndrome.

引用

页码：369 / 372

页数：4

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[1] Sebaceous gland tumor with a rare gene mutation within a tumor syndrome: Muir-Torre syndrome [Talgdrüsenkarzinom mit seltener Genmutation im Rahmen eines Tumorsyndroms: Muir-Torre-Syndrom]
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