Spraul C W, Jakobczyk-Zmija M J, Lang G K
Universitäts-Augenklinik Ulm.
Klin Monbl Augenheilkd. 1999 Nov;215(5):319-20. doi: 10.1055/s-2008-1034722.
A 61-year-old man was evaluated for a yellow tumor located at the lid margin of his lower eyelid, which had recurred for the second time after surgical excision. The patient's ocular examination was otherwise unremarkable as was the general examination with the exception of the presence 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.
When one encounters a sebaceous tumor involving the eyelid the possibility 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, or a carcinoma) and a minimum of one internal malignancy.
一名61岁男性因下眼睑睑缘处的黄色瘤接受评估,该黄色瘤在手术切除后复发第二次。除结肠有息肉和有多个结直肠癌家族史外,患者的眼部检查及全身检查均无异常。切除眼睑肿瘤,组织学检查显示为皮脂腺增生。
当遇到累及眼睑的皮脂腺肿瘤时,应考虑穆尔-托里综合征的可能性。穆尔-托里综合征是一种常染色体显性遗传性皮肤病,其特征为至少有一个皮脂腺肿瘤(增生、腺瘤、上皮瘤或癌)以及至少一种内脏恶性肿瘤。