CC BY-NC-ND 4.0 · Asian J Neurosurg 2022; 17(02): 235-241
DOI: 10.1055/s-0042-1750804
Original Article

Long-Term Surgical Outcomes of Two Patients with Intracranial Extraskeletal Mesenchymal Chondrosarcoma and a Brief Literature Review

1   Department of Neurosurgery, Istanbul Training and Research Hospital, Samatya, Istanbul, Turkey
› Author Affiliations

Abstract

Objective Intracranial extraskeletal mesenchymal chondrosarcomas (IEMCs) are malignant aggressive neoplasms. IEMCs originate from the meninges or parenchyma. In the current study, we aimed to figure out the importance of gross total resection (GTR) and adjuvant radiotherapy (RT) by evaluating all reported IEMCs through the literature that included our two patients.

Methods and Methods We presented two IEMC patients who were treated at our institutions and followed up for a long duration. To understand the appropriate management for IEMC, we conducted a systematic literature review for previously reported series and cases of IEMCs.

Results We surgically treated two young males with IEMC initially diagnosed at their age of 18 and 20 years. The patients were initially treated with GTR and GTR followed by RT, and followed-up for 218 and 73 months, respectively. Through both the patients, we obtained 83 reported IEMC patients from the literature. The mean age of the reported cases was 24.5 ± 16.0 years (2 months–71 years). Female predominance was 54.2%. The mean progression-free and overall survivals were 27.9 and 39.0 months, respectively. The progressiveness rate was 56%. The presence of progressiveness was a poor prognostic factor (p = 0.0008). GTR was achieved in 53.0% of the patients. There was a significant difference between patients who received GTR compared with those who did not receive GTR (p = 0.035).

Conclusion Regarding their malignancy and progressiveness, we recommended the maximal surgical resection with wide margins followed by RT as appropriate management for IEMCs with close follow-up. The timely treatment provides high life quality and avoids life-threatening complications.

Informed Consent

We obtained written informed consent from both patients and their relatives for publication of their cases and accompanying images.




Publication History

Article published online:
26 August 2022

© 2022. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Kan Z, Li H, Zhang J, You C. Intracranial mesenchymal chondrosarcoma: case report and literature review. Br J Neurosurg 2012; 26 (06) 912-914
  • 2 Dahlin DC, Henderson ED. Mesenchymal chondrosarcoma. Further observations on a new entity. Cancer 1962; 15: 410-417
  • 3 Tanvir I, Riaz S, Khan HA. et al. Mesenchymal chondrosarcoma arising in the central nervous system: a diagnostic pitfall. Int J Head Neck Surg 2013; 4 (03) 152-155
  • 4 Lightenstein L, Bernstein D. Unusual benign and malignant chondroid tumors of bone. A survey of some mesenchymal cartilage tumors and malignant chondroblastic tumors, including a few multicentric ones, as well as many atypical benign chondroblastomas and chondromyxoid fibromas. Cancer 1959; 12: 1142-1157
  • 5 Yan J, Cheng J, Li H. et al. Intraoperative high-field magnetic resonance imaging combined with neuronavigation-guided resection of intracranial mesenchymal chondrosarcoma in Broca's area: a rare case report and literature review. Int J Clin Exp Med 2015; 8 (03) 4697-4702
  • 6 Dutta G, Singh D, Saran RK, Singh H, Srivastava AK, Jagetia A. Metastasis from intracranial mesenchymal chondrosarcoma: report of a rare case. J Neurol Surg A Cent Eur Neurosurg 2019; 80 (01) 58-61
  • 7 Nagata S, Sawada K, Kitamura K. Chondrosarcoma arising from the falx cerebri. Surg Neurol 1986; 25 (05) 505-509
  • 8 Vergeer RA, Vink R, Avenarius JK, Driesse MJ. A 71-year-old woman with an intracranial dural-based mesenchymal chondrosarcoma. J Clin Neurosci 2012; 19 (08) 1170-1171
  • 9 Lin L, Varikatt W, Dexter M, Ng T. Diagnostic pitfall in the diagnosis of mesenchymal chondrosarcoma arising in the central nervous system. Neuropathology 2012; 32 (01) 82-90
  • 10 Xiao A, Li Z, He X, You C. A rare tentorial mesenchymal chondrosarcoma in posterior cranial fossa: case report. Neurol Neurochir Pol 2014; 48 (04) 287-291
  • 11 Nokes SR, Dauito R, Murtagh FR, Love LC, Arrington JA. Intracranial mesenchymal chondrosarcoma. AJNR Am J Neuroradiol 1987; 8 (06) 1137-1138
  • 12 Kubota T, Hayashi M, Yamamoto S. Primary intracranial mesenchymal chondrosarcoma: case report with review of the literature. Neurosurgery 1982; 10 (01) 105-110