Goutoudi P C, Sferopoulos N K, Papavasiliou V, Konstantinidis A
Department of Periodontology, Aristotle University of Thessaloniki, Greece.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1996 Jan;81(1):89-92. doi: 10.1016/s1079-2104(96)80155-7.
Diffuse skeletal cystic angiomatosis is an extremely rare disorder that has not previously been reported in detail in the dental literature. This case report deals with the oral manifestations in a 10-year-old boy. Clinical, radiographic, and computed tomographic examinations showed hyperplasia of the right side of the face. The computed tomographic imaging studies revealed the extent of the jawbone lesions and the adjacent hyperplastic soft tissues. The histologic appearance of the lesions, the course of the disease, and the differential diagnosis are discussed.
弥漫性骨骼囊性血管瘤病是一种极为罕见的疾病，此前牙科文献中尚未有详细报道。本病例报告涉及一名10岁男孩的口腔表现。临床、影像学和计算机断层扫描检查显示右侧面部增生。计算机断层扫描成像研究揭示了颌骨病变及相邻增生性软组织的范围。文中讨论了病变的组织学表现、疾病进程及鉴别诊断。
