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Giant cell tumor of the clivus: A case report and review of the literature

机译:锁骨巨细胞瘤:一例报道并文献复习

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摘要

Giant cell tumors (GCTs) mainly occur in metaphyses of long bones and are generally considered histologically benign; however, GCTs may be locally aggressive with a high rate of local recurrence and exhibit the potential for distant metastasis. Primary GCT of the clivus is extremely rare and is easily misdiagnosed and, thus, treatment remains controversial. The present report describes the case of a 22-year-old male with GCT located in the skull base originating from the clivus, with the involvement of multiple cranial nerves, which was successfully treated with transnasal transsphenoidal surgery following adjuvant radiotherapy and intravenous bisphosphonate administration. The patient remains symptom free at two years of follow-up. This report contributes to the limited literature regarding GCTs of the skull.
机译:巨细胞瘤(GCT)主要发生在长骨的干phy端,在组织学上通常被认为是良性的。但是,GCT可能具有高局部复发率,具有局部侵袭性,并且具有远处转移的潜力。锁骨的原发性GCT非常罕见,容易被误诊,因此治疗仍存在争议。本报告描述了一例22岁男性,其GCT位于源自锁骨的颅底,伴有多处颅神经受累,在辅助放疗和静脉注射双膦酸盐治疗后,经鼻经蝶窦手术成功治疗了该病例。两年的随访中患者无症状。该报告有助于有关颅骨GCT的文献有限。

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