颅内扩展性沙马瘤样幼年骨化性纤维瘤1例报告及系统评价

G. Jong-A-Liem, B. Nascimento, Carlos dos Reis Lisboa-Neto, J. Jesus, E. Bor-Seng-Shu, M. Teixeira, E. Figueiredo, E. Paschoal
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摘要

沙瘤样幼年骨化纤维瘤是一种罕见的纤维骨性肿瘤,具有侵袭性,但本质上是良性的。其侵袭性路径可导致面部变形、眼球突出和颅内扩张的发展,从而导致各种神经系统症状。根据Medline, EMBASE和Lilacs的MOOSE指南进行系统评价,结果报告了23例颅内延伸性PJOF。因此,我们发现这是相关的报告,提出一个15岁的男性面部变形和左眼突出,无视觉障碍的PJOF。病变出现在左前颅底,并延伸到眶内间隙和颧弓上方。通过对完全切除的病变进行组织病理学分析,诊断为PJOF。随访记录面部畸形无明显消退,术后图像显示病变完全切除。我们的病例提高了对这种罕见肿瘤的认识,它可能与脑膜瘤或其他颅内肿瘤混淆。
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Intracranial extended Psammomatoid Juvenile Ossifying Fibroma: case report and systematic review
Psammomatoid Juvenile Ossifying Fibroma is an uncommon fibro-osseous neoplasm of aggressive but benign nature found in the younger age. Its aggressive path can lead to facial deformation, eye proptosis, and development of intracranial extensions leading to various neurological symptoms. A systematic review based by the MOOSE guideline in Medline, EMBASE and Lilacs, resulted in 23 reported cases of intracranial extended PJOF. Hence, we found it relevant to present a case report of a 15-year-old male with facial deformation and left eye proptosis absent of visual disturbances with PJOF. The lesion was present in the left anterior base of the skull and extended to the intra-orbital space and over the zygomatic arch. The diagnosis was only confirmed as PJOF by histopathological analysis of the completely resected lesion. Follow up visits documented unremarkable regression of the facial deformity and post-op images showed a completely resected lesion. Our case raises the need to be aware of this rare tumor that can be confused with a meningioma or other intracranial tumors.
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