Abstract

Background.Hemangiopericytoma is a rare type of tumor of vascular origin and unknown malignant potential.Case Report.The article presents clinical case which is rarely observed, especially in children. A 12-year-old boy was admitted to Research Institute of Pediatric Oncology and Hematology with results of head MRI performed at a local clinic which demonstrated presence of a tumor of parameningeal localization. A patient passed complete clinical examination including some radiation diagnostic techniques, MRI, morphological, and immunohistochemical analyses and was diagnosed with sinonasal hemangiopericytoma of parameningeal localization T1bN0M0. The examination schedule, tactics, and treatment methods were selected individually for this patient since a commonly acknowledged treatment method had not been developed due to the lack of statistically relevant number of patient cases. Basing on the data on disease treatment records in Europe and Russia, patient received a complex treatment: three courses of neoadjuvant polychemotherapy, transnasal resection of tumor, and radiotherapy on the primary focus.Conclusion.At present the patient is alive with no sign of initial disease. The forecast is favourable. Effectiveness of complex treatment of patients with sinonasal hemangiopericytoma was demonstrated. The primary role of endonasal surgery during treatment of sinonasal hemangiopericytoma in a 12-year-old patient was indicated.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.