Cytological Features of Parachordoma: Two Case Reports of a Rare Entity
Parachordoma is an uncommon tumour of soft tissue of uncertain origin. Recurrence and metastasis are rarely seen. We report two cases with one presenting as recurrent case of pelvic parachordoma in a 45 year old female who presented with painless pelvic mass since 2 months. The other case repor...
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doaj-822711c079574bfdac4754d80a629e392020-11-25T00:12:45ZengKrishna Institute of Medical Sciences UniversityJournal of Krishna Institute of Medical Sciences University2231-42612231-42612016-04-0152140144Cytological Features of Parachordoma: Two Case Reports of a Rare EntityNeelam Sood0Kumar Sharad Sinha1Department of Pathology, Deen Dayal Upadhyay Hospital, Govt. of NCT, New Delhi- 110064(Delhi) IndiaDepartment of Pathology, Deen Dayal Upadhyay Hospital, Govt. of NCT, New Delhi- 110064(Delhi) IndiaParachordoma is an uncommon tumour of soft tissue of uncertain origin. Recurrence and metastasis are rarely seen. We report two cases with one presenting as recurrent case of pelvic parachordoma in a 45 year old female who presented with painless pelvic mass since 2 months. The other case report is of a 30 year male patient who presented with a diffuse swelling over left palmar aspect. Cytology findings of the pelvic swelling revealed moderately cellular smears composed of large physaliphorous cells with abundant bubbly cytoplasm in clusters and singly scattered medium sized epithelioid like cells with round nuclei, vesicular chromatin and prominent nucleoli in background of abundant myxoid ground substance. Cytology of the Palmar swelling revealed moderate cellularity comprised of oval to spindle shaped cells with coarse chromatin, prominent nucleoli and abundant vacuolated cytoplasm in a chondomyxoid stromal background. The preliminary diagnosis on cytology with further confirmation on histopathology with the aid of immunohistochemistry helped clinch the diagnosis of this rare entity of parachordoma occurring at unusual sites.http://www.jkimsu.com/jkimsu-vol5no2/JKIMSU,%20Vol.%205,%20No.%202,%20April-June%202016%20Page%20140-144.pdfCytologyRecurrentParachordomaPhysaliphorous |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Neelam Sood Kumar Sharad Sinha |
spellingShingle |
Neelam Sood Kumar Sharad Sinha Cytological Features of Parachordoma: Two Case Reports of a Rare Entity Journal of Krishna Institute of Medical Sciences University Cytology Recurrent Parachordoma Physaliphorous |
author_facet |
Neelam Sood Kumar Sharad Sinha |
author_sort |
Neelam Sood |
title |
Cytological Features of Parachordoma: Two Case Reports of a Rare Entity |
title_short |
Cytological Features of Parachordoma: Two Case Reports of a Rare Entity |
title_full |
Cytological Features of Parachordoma: Two Case Reports of a Rare Entity |
title_fullStr |
Cytological Features of Parachordoma: Two Case Reports of a Rare Entity |
title_full_unstemmed |
Cytological Features of Parachordoma: Two Case Reports of a Rare Entity |
title_sort |
cytological features of parachordoma: two case reports of a rare entity |
publisher |
Krishna Institute of Medical Sciences University |
series |
Journal of Krishna Institute of Medical Sciences University |
issn |
2231-4261 2231-4261 |
publishDate |
2016-04-01 |
description |
Parachordoma is an uncommon tumour of soft tissue
of uncertain origin. Recurrence and metastasis are
rarely seen. We report two cases with one presenting as
recurrent case of pelvic parachordoma in a 45 year old
female who presented with painless pelvic mass since
2 months. The other case report is of a 30 year male
patient who presented with a diffuse swelling over left
palmar aspect. Cytology findings of the pelvic
swelling revealed moderately cellular smears
composed of large physaliphorous cells with abundant
bubbly cytoplasm in clusters and singly scattered
medium sized epithelioid like cells with round nuclei,
vesicular chromatin and prominent nucleoli in
background of abundant myxoid ground substance.
Cytology of the Palmar swelling revealed moderate
cellularity comprised of oval to spindle shaped cells
with coarse chromatin, prominent nucleoli and
abundant vacuolated cytoplasm in a chondomyxoid
stromal background. The preliminary diagnosis on
cytology with further confirmation on histopathology
with the aid of immunohistochemistry helped clinch
the diagnosis of this rare entity of parachordoma
occurring at unusual sites. |
topic |
Cytology Recurrent Parachordoma Physaliphorous |
url |
http://www.jkimsu.com/jkimsu-vol5no2/JKIMSU,%20Vol.%205,%20No.%202,%20April-June%202016%20Page%20140-144.pdf |
work_keys_str_mv |
AT neelamsood cytologicalfeaturesofparachordomatwocasereportsofarareentity AT kumarsharadsinha cytologicalfeaturesofparachordomatwocasereportsofarareentity |
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1725397636780916736 |