• Yuichi Fujita, Yoichi Uozumi, and Takashi Sasayama.
• Department of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan. Electronic address: fyuichi@med.kobe-u.ac.jp.
• World Neurosurg. 2023 Feb 1; 170: 158162158-162.

AbstractA 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.Copyright © 2022 Elsevier Inc. All rights reserved.

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