加德纳综合征中的眼眶骨瘤。
Orbital osteoma in Gardner's syndrome.
作者信息
McNab A A
机构信息
Orbital, Plastic and Lacrimal Unit, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
出版信息
Aust N Z J Ophthalmol. 1998 May;26(2):169-70. doi: 10.1111/j.1442-9071.1998.tb01536.x.
PURPOSE
To report the association of an orbital osteoma with Gardner's syndrome (familial polyposis coli leading to carcinoma, multiple osteomas and skin and soft tissue tumours).
METHOD
A review of patient records.
RESULTS
A 29-year-old male with known Gardner's syndrome presented with long-standing right proptosis due to an osteoma of the medial wall and roof of the orbit. He had previously had prophylactic colectomy and one other osteoma of the skull excised.
CONCLUSION
Although orbital osteoma in the setting of Gardner's syndrome is rare, it should be recognized as an association because of the importance of the intestinal polyposis, which leads to carcinoma if untreated.
目的
报告眼眶骨瘤与加德纳综合征（家族性结肠息肉病导致癌症、多发骨瘤以及皮肤和软组织肿瘤）之间的关联。
方法
回顾患者病历。
结果
一名已知患有加德纳综合征的29岁男性，因眼眶内侧壁和眶顶骨瘤出现长期右眼球突出。他此前已接受预防性结肠切除术，并切除了另一处颅骨骨瘤。
结论
尽管加德纳综合征背景下的眼眶骨瘤罕见，但鉴于肠道息肉病的重要性（若不治疗会导致癌症），应认识到这种关联。
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