Subscribe to RSS
DOI: 10.1055/s-0040-1720990
Spontaneous Regression of a Clival Chordoma: An Unusual Case Report
Abstract
Introduction Chordoma is a malignant and aggressive tumor originating from remnants of the primitive notochord and usually involving the axial skeleton. Spontaneous regression of clival chordomas was described recently. We present the third case report of spontaneous regression of a clival chordoma and discuss similarities of cases and implications for clinical practice.
Case Description We present the case of a previously healthy 21-year-old Caucasian woman who presented with progressive holocranial headache for 3 months, which encouraged image investigation. Magnetic resonance imaging (MRI) revealed an osteolytic clival lesion hyperintense in T2 and hypointense in T1 images. After 2 months of initial evaluation and surgical proposal, she repeated MRI to allow use for intraoperative neuronavigation. Surprisingly, there was tumor regression.
Discussion The present reported case is somehow different from previous ones and does not share an underlying inflammatory/immunological recognizable fact, being interpreted by us as a spontaneous partial regression of the tumor. We highlight the need for continuous investigation of chordoma regression to uncover the underlying mechanisms.
Publication History
Received: 13 May 2020
Accepted: 25 August 2020
Article published online:
22 February 2021
© 2021. Thieme. All rights reserved.
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1 Bander ED, Kocharian G, Liechty B, Tsiouris AJ, Schwartz TH. Spontaneous regression of a clival chordoma. Case report. Acta Neurochir (Wien) 2020; 162 (02) 433-436
- 2 Bander ED, Schwartz TH. Response to: Letter to the Editor regarding: “Spontaneous regression of a clival chordoma. Case report.”. Acta Neurochir (Wien) 2020; 162 (02) 441
- 3 Passeri T, Giammattei L, Froelich S. Letter to the Editor regarding spontaneous regression of a clival chordoma. Case report. Acta Neurochir (Wien) 2020; 162 (02) 437-439
- 4 Radl R, Leithner A, Kastner N, Bodo K, Nader A, Windhager R. Disappearance of a cervical spine chordoma after nonoperative treatment. A case report. J Bone Joint Surg Am 2005; 87 (08) 1822-1827
- 5 Vellutini EAS, Brock RS, Martins HO, Taricco MA, de Oliveira MF. Diffuse spinal spreading following previous intracranial intradural chordoma resection: a rare case report. J Clin Neurosci 2019; 64: 44-46