Department of Neurosurgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, People's Republic of China.
Department of Neurosurgery, First Hospital of Nanping City, Nanping, Fujian, People's Republic of China.
World Neurosurg. 2019 Jul;127:469-477. doi: 10.1016/j.wneu.2019.04.075. Epub 2019 Apr 14.
Chondrosarcoma is a malignant tumor that originates from mesenchymal cells that have differentiated into chondrocytes, often growing laterally, rarely seen in the cranium, and seldom seen in the saddle area. We believe that only a few cases have been reported in the literature. We report a case of pituitary fossa chondrosarcoma, which was completely resected by an extended endoscopic endonasal approach, and a literature review.
A 20-year-old man was admitted to hospital with bilateral temporal headache and blurred vision, without any history of sexual dysfunction or diabetes insipidus. Endocrine function was normal. Computed tomography of the head showed calcified sellar lesions and sellar bone destruction, which were closely associated with the right cavernous sinus. Magnetic resonance imaging showed saddle area space-occupying lesions, with low signal on the T1-weighted image and high signal on the T2-weighted image, uneven enhancement by enhanced scanning, and unclear pituitary display. The tumor was completely resected by an extended endoscopic endonasal approach and confirmed by magnetic resonance imaging. Postoperative pathology revealed conventional chondrosarcoma (World Health Organization grade II). Postsurgical visual acuity also improved. The patient did not receive radiotherapy or chemotherapy. No recurrence was found at 10-month follow-up.
Sellar region chondrosarcoma is rare. For space-occupying lesions in this area, chondrosarcoma should be considered and not necessarily pituitary adenoma, craniopharyngioma, meningioma, and chordoma. The extended endoscopic endonasal approach represents a good treatment option for sellar area chondrosarcoma.
软骨肉瘤是一种起源于间充质细胞分化为软骨细胞的恶性肿瘤,通常侧向生长,颅少见,鞍区少见。我们认为文献中报道的病例很少。我们报告了一例垂体窝软骨肉瘤,采用扩大的内镜经鼻入路完全切除,并进行文献复习。
一名 20 岁男性因双侧颞部头痛和视力模糊入院,无性功能障碍或尿崩症病史。内分泌功能正常。头部 CT 显示鞍区钙化性病变和鞍底骨质破坏,与右侧海绵窦紧密相关。磁共振成像显示鞍区占位性病变,T1 加权像呈低信号,T2 加权像呈高信号,增强扫描不均匀强化,垂体显示不清。肿瘤采用扩大的内镜经鼻入路完全切除,并通过磁共振成像得到证实。术后病理显示常规软骨肉瘤(世界卫生组织 II 级)。术后视力也有所改善。患者未接受放疗或化疗。10 个月随访时未发现复发。
鞍区软骨肉瘤罕见。对于该区域的占位性病变,应考虑软骨肉瘤,而不一定是垂体腺瘤、颅咽管瘤、脑膜瘤和脊索瘤。扩大的内镜经鼻入路是治疗鞍区软骨肉瘤的一种较好的选择。