• 대한기관식도과학회지
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• 제4권2호
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• pp.249-253
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• 1998

Chondrosarcoma of bone commonly involve the pelvis, femur and shoulder girdle but the hyoid bone is a rare site for primary chondrosarcoma with approximately 10 cases having been reported in the literature. Radiologically it was well marginated and radiolucent mass with medullary bone destruction and central calcification. Wide surgical excision with or without radiotherapy is genera31y regarded as the treatment of choice for chondrosarcoma. Histopathology of chondrosarcoma was classified to clear cell chondrosarcoma, mucinous chondrosarcoma, dedifferentiated chondrosarcoma, and mesenchymal chondrosarcoma. We report a case of chondrosarcoma that originated from the right greater cornu of the hyoid bone, which underwent excision of the tumor with hemihyoidectomy and postoperative radiotherapy was performed.

• Clinical and Experimental Reproductive Medicine
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• 제49권4호
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• pp.285-288
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• 2022

Mesenchymal chondrosarcoma is a rare tumor that is more common in young people; it is an uncommon type of chondrosarcoma with a poor prognosis. In two-thirds of cases, it affects the bone, especially the spine. However, parts of the body other than the skeletal system are occasionally involved. These rarer types have a worse prognosis, with a high likelihood of metastasis and death. Due to the possible misdiagnosis of mesenchymal chondrosarcoma, the integrated use of imaging, immunohistochemistry, and pathology can be helpful.

• 대한골관절종양학회지
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• 제3권2호
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• pp.131-136
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• 1997

가톨릭 의과대학 정형외과에서는 32세 여자 환자의 제 12 흉추체에 발생한 발생 빈도가 드문, 일차성 연골 육종을 전방 도달법으로 추체 절제후 금속판 내고정과 함께 늑골 및 자가 해면골 이식술을 병행하여 치료후 42개월을 추적 관찰한 결과 국소재발 소견없이 정상생활 중이어서, 문헌고찰과 함께 보고하는 바이다.

• 대한골관절종양학회지
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• 제11권2호
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• pp.213-218
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• 2005

미분화 연골육종은 연골육종 중 가장 악성도가 높은 종양으로서, 연골육종의 약 10%에서 발생되는 것으로 알려져 있다. 미분화 연골 육종에 의해 발생된 악성종양은 방사선 및 화학요법에 반응을 하지 않아 광범위 종양 절제술만이 근치적 치료법이다. 본 연구는 근위 대퇴골에 발생한 저악성도 연골육종을 보존적으로 수술하고 추시 관찰 중, 골육종으로 미분화한 연골육종 1례를 보고하고자 한다.

• Journal of Korean Neurosurgical Society
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• 제53권1호
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• pp.46-48
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• 2013

Chondrosarcoma is a very uncommon malignant primary bone tumor, especially, it occurs extremely rare in the spine. A 52-year-old man was admitted to the emergency room with sudden paraplegia. Twelve hours prior to a paraplegic event, he visited an outpatient clinic with discomfort and tenderness around the medial border of the right scapular, and his neurologic status was absolutely intact. Magnetic resonance imaging showed a lobulated soft tissue mass from T3 to T5, which extended to the epidural space. Computed tomography scans showed soft tissue mass on the spinal posterior arch and osteolytic change of the adjacent bony structures. Emergent surgery was performed and the lesion was removed. Dark reddish blood and gel-like material were encountered around the dura and posterior arch during the operation. Multiple pulmonary nodules were found on a chest CT scan and a biopsy of one of them had been proven to be a metastasis of chondrosarcoma. The histologic examination showed dedifferentiated chondrosarcoma. The patient's neurologic deficit was improved slowly from ASIA A to ASIA D. Chondrosarcoma in the spine is extremely rare, even more with acute hemorrhage and sudden expansion into the epidural space. We named it chondrosarcoma apoplexy. We should consider the possibility of a hemorrhagic event when the patient's neurologic deficit worsens suddenly with spinal bone tumor.

• 대한골관절종양학회지
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• 제12권2호
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• pp.131-135
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• 2006

연골육종은 조직학적 소견에 따라 grade I, II, III로 나누어지며 예후와도 깊은 관련이 있다. Grade II 및 III의 연골육종의 수술 시 광범위 절제를 주로 시행하나 grade I 연골육종의 경우에는 소파술과 광범위 절제술 사이에 이견이 많다. 저자들은 상완골의 근위부에 grade I, 원위부에 grade II의 연골육종이 발생한 경우에 grade I은 소파술을, grade II는 광범위 절제술을 시행한 경험을 하였기에 보고하는 바이다.

• Journal of Chest Surgery
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• 제34권11호
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• pp.891-894
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• 2001

종격동의 연부조직에 발생한 간엽성 연골육종은 매우 드문 질환으로 후종격동에 발생한 골격외 간엽성 연골육종 1례를 치험하였기에 보고하는 바이다.

• Tuberculosis and Respiratory Diseases
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• 제52권6호
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• pp.645-650
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• 2002

저자들은 54세 여자 환자에서 좌상엽의 종괴에 대한 경피적 경흉 침생검을 통해 연골성 과오종으로 진단하고 방사선 소견상 폐결핵이 같이 의심되었으나 활동성 여부가 불분명하여 3개월 간격으로 외래 추적관찰 도중, 15개월째 객담 항산균 도말검사상 양성으로 판명되어 항결핵제를 투여하였으나, 21개월째 증상의 호전이 없고 종괴의 크기가 증가되는 소견을 보여 악성변화를 배제할 수 없어 수술을 시행하였으며, 조직검사상 만성 육아종성 병변과 함께 탈분화형 연골육종으로 과오종에서 악성화된 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• 대한세포병리학회지
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• 제8권2호
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• pp.194-198
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• 1997

Extraskeletal mesenchymal chondrosarcoma is a relatively rare tumor and its cytologic findings have rarely been reported. We experienced a case of mesenchymal chondrosarcoma of soft tissue of the right lateral neck diagnosed by fine needle aspiration biopsy in a 59 year-old man. Cytologic findings showed two cell components. One was an undifferentiated, small cell component with moderate amount of cytoplasm and spindle nuclei. The second population was a chondroid component. These cytologic findings were diagnostic to mesenchymal chondrosarcoma.

• 대한족부족관절학회지
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• 제6권1호
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• pp.129-133
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• 2002

Extraskeletal myxoid chondrosarcoma is an unusual soft tissue sarcoma with distinctive histologic features. It once was called chordoid sarcoma because it resembles chordoma histologically. The lesion has been shown to be of chondroblastic origin. This lesion shown to have ultrastructural and molecular features distinct from that of myxoid chondrosarcoma of bone. We report a case of extraskeletal myxoid chondrosarcoma in forefoot.