Department of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Department of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
World Neurosurg. 2023 Feb;170:158-162. doi: 10.1016/j.wneu.2022.11.031. Epub 2022 Nov 12.
A purely intrasellar chordoma is rare among skull base chordomas and is recognized as originating from ectopic embryological notochord located in the sella turcica. In view of its rarity and nonspecific symptoms, clinicians may misdiagnose intrasellar chordoma as pituitary adenoma based on preoperative radiographic images. In this report, we present an intrasellar chordoma that clinically mimicked pituitary macroadenoma with hyperprolactinemia and hypopituitarism and was successfully resected by endoscopic endonasal transsphenoidal surgery. This case demonstrated radiographic features that chordoma should be suspected in sellar lesions. The enlarged sellar with thinned remodeled bone without clival destruction was firstly reminiscent of pituitary adenoma, whereas the very high signal on T2-weighted images and heterogeneous enhancement characteristically suggested chordoma. This rare diagnosis must be considered in the preoperative evaluation of sellar lesions because it can affect how the neurosurgeon prepares for surgery and the surgical goals.
单纯鞍内脊索瘤在颅底脊索瘤中较为罕见,被认为起源于蝶鞍内异位胚胎脊索。鉴于其罕见性和非特异性症状,临床医生可能会根据术前影像学图像将鞍内脊索瘤误诊为垂体腺瘤。在本报告中,我们介绍了一例鞍内脊索瘤,其临床表现类似于伴有高泌乳素血症和垂体功能减退的垂体大腺瘤,并通过经鼻内镜蝶窦入路成功切除。该病例显示出脊索瘤在鞍区病变中的放射学特征,应予以怀疑。鞍内扩大伴变薄改建的骨质,无斜坡破坏,首先提示为垂体腺瘤,而 T2 加权图像上的高信号和不均匀强化特征提示脊索瘤。这种罕见的诊断在鞍区病变的术前评估中必须考虑,因为它会影响神经外科医生对手术的准备和手术目标。