The surgical extension of clivus chordoma with the use of the pf coblator is evaluated in this case study. Dysembryogenic tumours arising in the notochordal process are chordomas. With particular diagnostic and management problems, they are violent tumours. Because of their vital role and ability to recur, these tumours are difficult to manage; they have been treated with a combination of surgery and radiotherapy in recent years. As far as practicable, primary treatment is complete surgical removal of the tumour. The risk of recurrence after complete surgical resection is high. A 52-year-old female patient experienced symptoms of reduced right eye vision, nasal bleeding, nasal obstruction, and trouble swallowing.
Author(s) Details
Dr. Saloni Shah
B. J. Medical College, Civil Hospital, Ahmedabad, India.
Roma Gandhi
B. J. Medical College, Civil Hospital, Ahmedabad, India.
Hemang Brahmbahtt
B. J. Medical College, Civil Hospital, Ahmedabad, India.
Rajesh Viswakarma
ENT Department, Civil Hospital, Ahmedabad, India.
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