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Journal of Case Reports
Chordoma – FNAC Diagnosis: A Case Report and Review of Literature
Kuppili Venkata Murali Mohan1, Dabbiru Radhika2, Chakkirala Nalini Mohan1, Sanakkayala Rajkumari3, Jukuri Naganarasimha Raju4
From the Departments of Pathology1, Obstetrics & Gynaecology3, Radiology4,  Katuri Medical College, Guntur, Andhra Pradesh and Department of Anatomy2, Guntur Medical College, Guntur (AP), India.
Corresponding Author:
Dr. K.V.Murali Mohan
Email: kuppilimm@gmail.com
Received: 13-OCT-2014 Accepted: 20-OCT-2014 Published Online: 25-NOV-2014
DOI: http://dx.doi.org/10.17659/01.2014.0115
Abstract
Chordoma is a rare slow growing malignant tumor which arises from primitive notochord remnants. A fifty year female patient attended outpatient complaining of swelling in the low back, gradually increasing over a six years period, attained present size of 3×4 cm. Fine needle aspiration cytology revealed characteristic physaliphorous cells seen in chordoma. Histopathology confirmed the diagnosis of chordoma. 
Keywords : Chordoma, Neoplasms, Nervous System Neoplasms, Notochord, Cytodiagnosis, Humans.
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