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首页> 外文期刊>Surgical Neurology International >Transcranial resection of a juvenile psammomatoid ossifying fibroma of the orbit: A case report with 2-year follow-up
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Transcranial resection of a juvenile psammomatoid ossifying fibroma of the orbit: A case report with 2-year follow-up

机译:跨颅骨切除术治疗肉瘤的肉瘤纤维瘤:一个案例报告,2年后续随访

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Background: Juvenile psammomatoid ossifying fibromas (JPOFs) are benign, locally invasive lesion of the craniofacial skeleton that may undergo rapid growth resulting in damage to cranial and facial structures. They usually occur before the age of 15 years and should be carefully treated as their diagnosis may be confused with other lesions such as psammomatous meningioma. Case Description: A 14-year-old male presented to the clinic with a history of progressive left proptosis. Imaging studies revealed a well-circumscribed lesion involving the left orbital roof and showing internal areas of calcification and sclerosis. He underwent a transcranial resection of the lesion and follow-up imaging revealed no evidence of recurrence. Conclusion: JPOFs are locally invasive lesions that require careful diagnosis and meticulous excision to prevent recurrence.
机译:背景:少年PsammoMatoid ossify纤维瘤(JPOFS)是良性的,局部侵入性的颅面骨骼的患者可能经历快速增长,导致颅骨和面部结构损坏。它们通常发生在15岁以下,并且应仔细治疗,因为他们的诊断可能与母猪脑膜瘤等其他病变混淆。案例描述:一名14岁的男性呈现给诊所,具有逐步的左翼分子历史。成像研究揭示了涉及左侧轨道屋顶的良好围绕的病变,并显示出钙化和硬化症的内部区域。他经历了病变和后续成像的经颅切除,揭示了没有复发的证据。结论:JPOFS是局部侵入性病变,需要仔细诊断和细致的切除,以防止复发。

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