Background Patient: A 61-year-old man was evaluated for a yellow tumor loca
ted at the lid margin of his lower eyelid, which had recurred for the secon
d time after surgical excision. The patient's ocular examination was otherw
ise unremarkable as was the general examination with the exception of the p
resence of a polyp in the colon and a family history of multiple colorectal
carcinomas. The eyelid tumor was excised and histologic examination showed
a sebaceous hyperplasia.
Conclusion When one encounters a sebaceous tumor involving the eyelid the p
ossibility of Muir-Torre syndrome should be considered. Muir-Torre syndrome
is an autosomal dominant genodermatosis characterized by at least a single
sebaceous gland tumor (either a hyperplasia, an adenoma, an epithelioma, o
r a carcinoma) and a minimum of one internal malignancy.