Gündüz Kaan, Palamar Melis, Parmak Neslihan, Kuzu Işinsu
Department of Ophthalmology, Ankara University Faculty of Medicine, Ankara, Turkey.
J AAPOS. 2007 Oct;11(5):506-8. doi: 10.1016/j.jaapos.2007.03.016. Epub 2007 May 24.
We present clinical, radiological, and histopathological findings and treatment results of two infants with orbital eosinophilic granuloma. Both patients presented at 1 year of age with unilateral proptosis, periorbital edema, and a superotemporally located, ill-defined orbital mass on computed tomographic (CT) imaging, with bone erosion in one patient. After subtotal excision, histopathological examination revealed eosinophilic granuloma, and the proptosis resolved with no sign of orbital tumor recurrence or systemic involvement at 12 and 23 months follow-up. Eosinophilic granuloma is a rare childhood orbital tumor that may or may not present with osteolytic change.
我们报告了两名患有眼眶嗜酸性肉芽肿婴儿的临床、放射学和组织病理学检查结果及治疗效果。两名患者均在1岁时出现单侧眼球突出、眶周水肿,计算机断层扫描(CT)成像显示眶内有一位于颞上象限、边界不清的肿块,其中一名患者伴有骨质侵蚀。次全切除术后,组织病理学检查显示为嗜酸性肉芽肿,在12个月和23个月的随访中,眼球突出症状消失,无眼眶肿瘤复发或全身受累迹象。嗜酸性肉芽肿是一种罕见的儿童眼眶肿瘤,可能伴有或不伴有溶骨性改变。