Covid Alert

Print ISSN:-2394-6784

Online ISSN:-2394-6792


Current Issue

Year 2020

Volume: 7 , Issue: 2

Article Access statistics

Viewed: 115

Emailed: 0

PDF Downloaded: 69

Indian Journal of Pathology and Oncology

Chondroid chordoma- A rare tumor diagnosed on cytology: A case report

Full Text PDF Share on Facebook Share on Twitter

Case Report

Author Details : Anshul Singh, Himalina Sangma*, Vasudha Singh, Vatsala Misra

Volume : 7, Issue : 2, Year : 2020

Article Page : 312-316

Suggest article by email


Chordomas are rare, malignant and locally aggressive tumors that are derived from the remnants of
primitive notochord, out of which chondroid chordomas are even rarer. Very few case reports have described
this variant, which is difficult to pick up on cytopathology alone and has a number of other differentials too.
We report here a case of chondroid chordoma at the sacrococcygeal region that was diagnosed on FNAC
in an elderly male patient emphasizing on its cytomorphology and how to differentiate from its cytological

Keywords: FNAC, notochordal tumors, Cartilaginous, Physaliphorous.

Doi : 10.18231/j.ijpo.2020.060

How to cite : Singh A, Sangma H, Singh V, Misra V, Chondroid chordoma- A rare tumor diagnosed on cytology: A case report. Indian J Pathol Oncol 2020;7(2):312-316

Copyright © 2020 by author(s) and Indian J Pathol Oncol. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC-BY-NC 4.0) (