Walther E K
Universitäts-Hals-Nasen-Ohrenklinik Bonn.
Laryngorhinootologie. 1993 Mar;72(3):136-9. doi: 10.1055/s-2007-997871.
A case of a rare subtype of midfacial ossifying fibroma in a 5-year old child is presented. Fibro-osseous lesions represent a variety of bone proliferations each characterised by different morphological patterns of osteoid production. Psammomatoid ossifying fibroma is characterised histologically by numerous small round ossicles resembling psammoma bodies and is a locally invasive lesion of facial and cranial bones. The histopathology is described. The surgical treatment includes complete resection of the tumour as well as involved bones by means of midfacial degloving. Two years after surgical treatment the child is free from symptoms and tumour recurrence.
本文报告了一例5岁儿童罕见亚型的面中部骨化性纤维瘤病例。纤维-骨病变代表多种骨增殖,每种都以不同的类骨质生成形态模式为特征。砂粒样骨化性纤维瘤在组织学上的特征是有许多类似砂粒体的小圆形骨小体,是面部和颅骨的局部侵袭性病变。文中描述了其组织病理学。手术治疗包括通过面中部去套状手术完整切除肿瘤及受累骨骼。手术治疗两年后,患儿无症状且肿瘤无复发。