Giant cell tumor of skull base: Management and review of literature

G. Pemmaraju, Anuradha Singh, Anand Parab, Shubhangi Barsing
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Abstract

Giant cell tumors (GCTs) of bone constitute 3%–5% of all the bone tumors. GCTs are uncommon, locally aggressive, osteolytic neoplasms commonly seen in early adulthood. Involvement of cranial and facial bones is rare and comprises 2% of all the cases. Sphenoid and temporal bones are the most common sites of GCTs in head and neck. Although complete resection may not be possible, feasibility of partial resection depending on the extent and involvement of critical structures should be the best alternative. GCTs, though historically considered radioresistant, have a dose-dependent effect. This is a case report of a 20-year-old male, who presented with headache, blurring of vision in both the eyes, and diplopia for 2 months. Magnetic resonance imaging (MRI) showed a 4.5 cm × 3.4 cm × 3.5 cm lesion involving superior body of clivus, sphenoid sinus, and floor of sella, adherent to anterior pituitary gland along the superior aspect, indenting optic chiasm with extrinsic compression and bulging into bilateral cavernous sinuses. The patient underwent endoscopic transnasal partial resection of the lesion. Histopathological examination showed tissue containing numerous osteoclasts such as giant cells separated by round to spindle-shaped mononuclear cells. On immunohistochemistry, the giant cells were positive for CD 68 with Ki 67 proliferation index about 15%–20% in highest proliferating areas. The patient underwent definitive radiation treatment to a radiation dose of 55 Gy in 31 fractions over 6 weeks. The patient tolerated treatment well with minimal toxicities, his vision improved by the end of treatment. The patient needs to be assessed for radiological response and late side effects. GCTs of the skull are rare benign osteolytic locally aggressive lesions generally seen in early adulthood. En bloc surgical resection is the treatment of choice but has high local recurrence rates. Radiation is the treatment of choice in unresectable, partially resected, and recurrent tumors. With the advent of advanced techniques such as intensity-modulated radiotherapy/volumetric-modulated arc therapy, better dose distribution can be achieved in the target minimizing dose to the critical structures. Imaging with daily kilovolt cone-beam computed tomography is essential in the treatment of tumors of the skull for precise treatment delivery.
颅底巨细胞瘤:治疗及文献回顾
骨巨细胞瘤(gct)占骨肿瘤的3%-5%。gct是罕见的,局部侵袭性的溶骨性肿瘤,常见于成年早期。累及颅面骨是罕见的,占所有病例的2%。蝶骨和颞骨是头颈部gct最常见的部位。虽然完全切除可能是不可能的,但部分切除的可行性取决于关键结构的程度和受累程度,应该是最好的选择。虽然历史上认为gct具有放射抗性,但它具有剂量依赖性。这是一个20岁男性的病例报告,他表现为头痛、双眼视力模糊和复视2个月。磁共振成像(MRI)显示,病变面积为4.5 cm × 3.4 cm × 3.5 cm,累及斜坡上体、蝶窦及蝶鞍底,沿上侧壁附着垂体前叶,缩进视交叉伴外源压迫,向双侧海绵窦膨出。患者接受内镜经鼻部分切除病变。组织病理学检查显示组织中含有大量的破骨细胞,如巨细胞,由圆形到纺锤形的单核细胞分开。免疫组化结果显示,巨细胞cd68阳性,Ki - 67增殖指数在增殖高峰区约为15% ~ 20%。患者在6周内接受了31次放射治疗,放射剂量为55 Gy。患者对治疗耐受良好,毒性最小,治疗结束时视力有所改善。需要评估患者的放射反应和后期副作用。颅骨gct是一种罕见的良性溶骨局部侵袭性病变,通常见于成年早期。整体手术切除是治疗的选择,但有很高的局部复发率。放疗是不可切除、部分切除和复发肿瘤的首选治疗方法。随着调强放疗/调容电弧治疗等先进技术的出现,可以在靶区实现较好的剂量分布,使对关键结构的剂量最小化。每日千伏特锥束计算机断层扫描成像是必要的治疗颅骨肿瘤的精确治疗交付。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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