A watch, wait, and rescan approach for incidental benign-appearing notochordal lesions of the skull base

Author:

Usher Inga E.12,Drosos Evangelos1,Morsy Abdalla1,Wadeson Andrea1,Laitt Roger1,Abdulla Sarah1,Madhavan Aparna1,Halliday Jane1,Rutherford Scott1,King Andrew T.12,Pathmanaban Omar N.12

Affiliation:

1. Manchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust, Salford, Manchester;

2. Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Division of Neuroscience, School of Biological Sciences, University of Manchester, United Kingdom

Abstract

OBJECTIVE The aim of this study was to describe the natural history of incidental benign-appearing notochordal lesions of the skull base with specific attention to features that can make differentiation from low-grade chordoma more difficult, namely contrast uptake and bone erosion. METHODS In this retrospective case series, the authors describe the clinical outcomes of 58 patients with incidental benign-appearing notochordal lesions of the clivus, including those with minor radiological features of bone erosion or contrast uptake. RESULTS All lesions remained stable during a median follow-up of almost 3 years. Thirty-seven (64%) patients underwent contrast-enhanced MRI; lesions in 14 (38%) of these patients exhibited minimal contrast enhancement. Twenty-seven (47%) patients underwent CT; lesions in 6 (22%) of these patients exhibited minimal bone erosion. CONCLUSIONS These data make the case for monitoring selected cases of benign-appearing notochordal lesions of the clivus in the first instance even when there is minor contrast uptake or minimal bone erosion.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Reference23 articles.

1. Benign notochordal cell tumour;Yamaguchi T,2020

2. Chordoma: incidence and survival patterns in the United States, 1973-1995;McMaster ML,2001

3. Building a global consensus approach to chordoma: a position paper from the medical and patient community;Stacchiotti S,2015

4. Conventional chordoma. In: Soft Tissue and Bone Tumours: WHO Classification of Tumours;Tirabosco R,2020

5. Notochordal tumors;Tirabosco R,2021

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