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Solitary Osteochondroma of the Skull Base: A Case Report and Literature Review

机译:颅底孤立性骨软骨瘤:一例报道并文献复习

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摘要

We report a case of an osteochondroma in the posterior clinoid process that occurred in a 43-year-old man with trochlear nerve palsy. Although the potential preoperative diagnoses based on computed tomography and magnetic resonance imaging included other intracranial tumors such as calcified meningioma, thallium-201 single-photon emission computed tomography effectively differentiated osteochondroma from those possibilities. Via an orbitozygomatic approach, a subtotal resection was achieved with a good relief of symptoms. Twenty-two cases of solitary osteochondromas in the skull base have been reported that have demonstrated little risk of recurrence or malignant transformation. However, surgery for skull base osteochondromas does carry a significant risk with a reported mortality > 10%. Although some previous reports advocate complete resection as the only curative method for skull base osteochondromas, the risks of total resection should be weighed against the chance for recurrence; our review of the literature demonstrated a relatively high mortality and an extremely low incidence of recurrence.
机译:我们报告了发生在一名43岁男性滑车神经麻痹的后斜突过程中的骨软骨瘤病例。尽管基于计算机断层扫描和磁共振成像的术前诊断可能包括其他颅内肿瘤,例如钙化脑膜瘤,但th 201单光子发射计算机断层扫描有效地将骨软骨瘤与这些可能性区分开来。通过眶oz入路的方法,可以实现大部切除,并且可以很好地缓解症状。据报道,有22例颅底孤立性骨软骨瘤病例复发或恶变的风险很小。但是,颅底骨软骨瘤的手术确实有很大的风险,据报道死亡率> 10%。尽管以前的一些报道主张完全切除是颅底骨软骨瘤的唯一治疗方法,但应权衡完全切除的风险与复发的机会。我们对文献的回顾显示出较高的死亡率和极低的复发率。

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