| Literature DB >> 33005621 |
Frederick A Jakobiec1, Paula Cortes Barrantes1, Tatyana Milman2, Michael Yoon3.
Abstract
Over a period of 1 year, a 74-year-old man slowly developed a painless left upper eyelid intratarsal mass. The skin was movable over the lesion. At surgery, a well-circumscribed, yellow-white, partially cystic tumor was encountered. Histopathologically it was composed of a random mixture of basaloid and sebaceous cells arranged in interconnecting cords. Immunohistochemical evaluation disclosed epithelial membrane antigen, adipophilin, and cytokeratin 14 positivity. These findings led to the diagnosis of a sebaceoma. The tumor cells abnormally failed to express mismatch repair proteins for MLH1 and PMS2. The patient did not have a personal history of any visceral malignancy, but his father had died at the age of 46 years and a daughter at the age of 33 years from colonic carcinomas. The implications of this periocular sebaceoma for the Muir-Torre syndrome are explored.Entities:
Keywords: Eyelid; Meibomian gland; Mismatch repair proteins; Muir-Torre syndrome; Sebaceoma; Sebaceous adenoma; Sebaceous carcinoma; Sebaceous hyperplasia
Year: 2020 PMID: 33005621 PMCID: PMC7506298 DOI: 10.1159/000504627
Source DB: PubMed Journal: Ocul Oncol Pathol ISSN: 2296-4657