Cytologic Findings of Chordoma in Fine Needle Aspiration Cytology

척삭종의 세침흡인 세포학적 소견

  • Ryu, Han-Suk (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Kim, Min-Suk (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Ha, Hwa-Jung (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Kim, Jung-Soon (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Shin, Myung-Soon (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Park, Sun-Hoo (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Chung, Jin-Haeng (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Koh, Jae-Soo (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences) ;
  • Lee, Seung-Sook (Department of Pathology, Korea Cancer Center Hospital, Korea Institut of Radiological & Medical Sciences)
  • 유한석 (원자력의학원 원자력병원 병리과) ;
  • 김민석 (원자력의학원 원자력병원 병리과) ;
  • 하화정 (원자력의학원 원자력병원 병리과) ;
  • 김정순 (원자력의학원 원자력병원 병리과) ;
  • 신명순 (원자력의학원 원자력병원 병리과) ;
  • 박선후 (원자력의학원 원자력병원 병리과) ;
  • 정진행 (원자력의학원 원자력병원 병리과) ;
  • 고재수 (원자력의학원 원자력병원 병리과) ;
  • 이승숙 (원자력의학원 원자력병원 병리과)
  • Published : 2004.05.30

Abstract

It is important to recognize the pathognomonic cytologic findings of chordoma, because of overlapping cytologic features between chordoma, chondrshdosarcoma, myxofilbrillary ependymoma, and metastatic adenocarcinoma. We reviewed the cytomorphologic features of 5 cases of chordoma diagnosed by fine needle aspiration cytology at Korean Cancer Center Hospital from 1987 to 2003. Clinical and radiographic findings of each case were reviewed. Four males and one female (29-54 years) had tumors involving the sacrum. Pain was the presenting symptom in 4 cases. The three cases showed moderate to high cellularity. In all cases, typical physaliferous cells with or without cytoplasmic processes were noted. In two cases, the background was myxoid with single scattered cells. Cell clusters showing cord-like arrangement were occasionally seen. The single or clustered cells showed mild cellular pleomorphism with slightly increased nuclear/cytoplasmic ratio. Mitotic figures were not seen. In our review, the recognition of physaliferous cells is the most important feature to diagnose chordoma and to differentiate it from other lesions mimicking chordoma.

Keywords

References

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