Solitary fibrous tumor/hemangiopericytoma of the cervical spine: A systematic review of the literature with an illustrative case

Author:

Colamaria Antonio1,Carbone Francesco2,Sacco Matteo1,Corsi Fabrizio3,Leone Augusto4,Parbonetti Giovanni5,de Notaris Matteo5,Fochi Nicola Pio2,Landriscina Matteo6,Coppola Giulia7,de Santis Elena8,Giordano Guido6

Affiliation:

1. Department of Neurosurgery, Riuniti Hospital, Foggia, Italy

2. Department of Neurosurgery, University of Foggia, Foggia, Italy

3. Department of Pathology, “Riuniti” Hospital, Foggia, Italy,

4. Department of Neurosurgery, Städtisches Klinikum Karlsruhe, Karlsruhe, Germany,

5. Department of Neurosurgery, Division of Neurosurgery, San Pio Hospital, Benevento, Italy

6. Department of Medical Oncology and Bimolecular Therapy, “Riuniti” Hospital, Foggia,, Italy

7. Department of Radiological, Oncological and Pathological Sciences, La Sapienza University, Roma, Lazio, Italy

8. Department of Anatomical, Histological, Forensic Medicine and Orthopedic sciences, La Sapienza University, Roma, Lazio, Italy.

Abstract

Background: In the WHO 2016 classification of central nervous system tumors, solitary fibrous tumors (SFT) and hemangiopericytomas (HPC) were considered part of the same category given a shared mutation. Nevertheless, since the new 2021 WHO classification, the term “hemangiopericytoma” has been retired, and SFT is considered an independent pathological entity. Methods: We reviewed the literature following preferred reporting items for systematic reviews and meta-analyses guidelines focusing on the treatment options and prognosis of patients with cervical SFT. We also present a 68-year-old female with spinal intradural extramedullary SFT complicated by diffuse extension into paravertebral tissues and muscles. Results: We found 38 cervical SFT in the literature. Patients averaged 47.3 years of age and 47.4% were female. Typically, these lesions spanned two spinal levels resulting in cord compression and most frequently exhibited benign features (i.e., diagnosed as Grade I SFTs). Interestingly, two patients exhibited distant metastases and had initial pathology consistent with grade II SFT. Conclusion: SFT of the cervical spine is rare and its management varies according to the histological grade and the clinical behavior, generally warranting surgical excision and adjuvant radiation therapy and/or systemic chemotherapy.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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