Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2011-4-13
pubmed:abstractText
Chondroblastic osteosarcoma (OS) accounts for about 25% of all cases of OS. It can pose diagnostic difficulty on cytology, as the tumor cells may resemble the carcinomatous cells. We present a case of a 35-year-old female patient who presented with a firm swelling in the left temporal region. On fine-needle aspiration, the smears revealed abundant cellularity with tumor cells showing significant nuclear pleomorphism and multinucleation. The tumor cells had abundant foamy to vacuolated cytoplasm, thereby indicating sebaceous differentiation and it was cytologically interpreted as sebaceous carcinoma. However, on subsequent histopathology, similar tumor cells were seen lying down abundant amount of osteoid material along with foci of chondroid differentiation and was diagnosed as chondroblastic OS. Pitfalls in the cytodiagnosis of this case along with differential diagnosis on cytology are discussed.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1097-0339
pubmed:author
pubmed:copyrightInfo
Copyright © 2010 Wiley-Liss, Inc.
pubmed:issnType
Electronic
pubmed:volume
39
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
377-9
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Chondroblastic osteosarcoma of the temporal region: a diagnostic dilemma.
pubmed:affiliation
Department of Cytology and Gynecological Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India. nalini203@rediffmail.com
pubmed:publicationType
Journal Article, Case Reports