Juvenile psammomatoid ossifying fibroma of the neurocranium -: Report of four cases

被引:20
作者
Hasselblatt, M
Jundt, G
Greiner, C
Rama, B
Schmäl, F
Iglesias-Rozas, JR
van de Nes, JAP
Paulus, W
机构
[1] Univ Hosp Munster, Inst Neuropathol, D-48149 Munster, Germany
[2] Univ Hosp Munster, Dept Neurosurg, D-48149 Munster, Germany
[3] Univ Hosp Munster, Dept Otorhinolaryngol, D-48149 Munster, Germany
[4] Paracelsus Clin, Dept Neurosurg, Osnabruck, Germany
[5] Katharinen Hosp, Inst Pathol, D-70174 Stuttgart, Germany
[6] Univ Hosp Essen, Inst Neuropathol, Essen, Germany
[7] Univ Clin, Kantonsspital, Inst Pathol, Bone Tumor Reference Ctr, CH-4031 Basel, Switzerland
关键词
juvenile psammornatoid ossifying fibroma; meningioma; fibrous dysplasia; children;
D O I
10.3171/jns.2005.102.6.1151
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Juvenile psammomatoid ossifying fibroma (JPOF) is a benign fibroosseous lesion predominantly arising within the paranasal sinuses in children and Young adults. Neurocranial occurrence is exceedingly rare and a location within the neurocranial portion of the temporal bone has not been described. The authors report on one case of sinonasal JPOF secondarily extending into the cranial cavity and three cases primarily affecting the neurocranial bones to increase clinical awareness of this uncommon tumor, which may be easily mistaken for meningioma. Moreover, the absence of activating missense mutations of the GNAS1 gene in two cases strongly argues against a relationship between JPOF and fibrous dysplasia.
引用
收藏
页码:1151 / 1154
页数:4
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