Ossifying fibroma of the skull in a patient with neurofibromatosis type 1 - Case report

被引:21
|
作者
Ruggieri, M
Pavone, V
Tine, A
Polizzi, A
Magro, G
Duray, PH
Merino, M
Albanese, V
机构
[1] UNIV CATANIA, INST NEUROSURG, CATANIA, ITALY
[2] OXFORD RADCLIFFE HOSP, DEPT CLIN GENET, OXFORD, ENGLAND
[3] NIH, DEPT HLTH & HUMAN SERV, PATHOL LAB, BETHESDA, MD 20892 USA
关键词
neurofibromatosis; fibrous dysplasia;
D O I
10.3171/jns.1996.85.5.0941
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Ossifying fibroma is a rare, benign, primary bone tumor that occurs most commonly in the mandible; a cranial vault location is extremely rare. In this report a case of symptomatic frontoparietotemporal ossifying fibroma with intracranial growth and cerebral displacement in a 12-year-old boy with neurofibromatosis type 1 (NF1) is described. Once excised the lesion did not recur. The skeletal system is frequently affected in NF1, and bone abnormalities are present in 50% to 70% of patients with this condition. The etiology of such lesions in NF1 is still controversal. To the authors' knowledge, ossifying fibromas of calvarial bones have not been described in NF1.
引用
收藏
页码:941 / 944
页数:4
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