SACROCOCCYGEAL CHORDOMA: A RARE CASE REPORT DIAGNOSED ON CYTOLOGY

Author:

Gill Meenu1,Budhwar Archana2,Gupta Sumiti3,Jain Promil4

Affiliation:

1. Professor, Department of Pathology, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak- 124001, Haryana. (India)

2. Senior Resident, Department of Pathology, VMMC & Safdarjung Hospital, New Delhi110029. (INDIA)

3. Professor, Department of Pathology, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak- 124001, Haryana. (India).

4. Associate Professor, Department of Pathology, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak- 124001, Haryana. (India)

Abstract

Chordomas are rare malignant tumors of notochordal origin. They commonly arise in 5th and 6th decade with a male predominance of 3:1. They have indolent nature and rarely metastasize. We report a case of 71 year old male presenting with lower backache diagnosed as Chordoma on FNAC and later conrmed on histopathology.

Publisher

World Wide Journals

Subject

General Economics, Econometrics and Finance,General Social Sciences,Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health,Multidisciplinary,General Chemical Engineering,Law,Surfaces, Coatings and Films,General Energy,Mechanical Engineering,Industrial and Manufacturing Engineering,Strategy and Management,Computer Science Applications,Industrial relations,Management Information Systems,Marketing,General Engineering,Developmental and Educational Psychology,Education,Engineering (miscellaneous),Instrumentation

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