Bardenstein D S, McLean I W, Nerney J, Boatwright R S
Armed Forces Institute of Pathology, Washington, DC 20306-6000.
Ophthalmology. 1988 Aug;95(8):1038-41. doi: 10.1016/s0161-6420(88)33066-6.
Cowden's disease, or multiple hamartoma syndrome, is a rare genodermatosis. Multiple facial trichilemmomas, acral keratoses, and oral papillomas are the most common mucocutaneous lesions in this disease. It is associated with increased rates of cancer of the breast and thyroid as well as benign tumors and hamartomas of multiple organ systems. Multiple facial trichilemmomas are essentially pathognomonic of this syndrome and may appear as lesions of the eyelid and periorbital skin. A case of Cowden's disease is described and previously reported cases reviewed, with emphasis on the ocular aspects of the disease.
考登病,即多发性错构瘤综合征,是一种罕见的遗传性皮肤病。多发性面部毛发上皮瘤、肢端角化病和口腔乳头状瘤是该疾病最常见的黏膜皮肤病变。它与乳腺癌和甲状腺癌的发病率增加以及多器官系统的良性肿瘤和错构瘤有关。多发性面部毛发上皮瘤本质上是该综合征的特征性表现,可能表现为眼睑和眶周皮肤的病变。本文描述了一例考登病病例,并回顾了既往报道的病例,重点关注该疾病的眼部表现。