• 대한골관절종양학회지
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• 제1권2호
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• pp.249-253
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• 1995

The fibrous dysplasia is a progressive and disabling condition that lead to deformity, especially weight bearing bones. The morbidity that is associated with the polyostotic fibrous dysplasia is the recurrent fracture and deformity. Various methods of treatment had been failed to control this problem. We used osteotomy and reconstruction nailing for polyostotic fibrous dysplasia occured in the proximal part of right femur with varus deformity and reconstruction nailing in left femur without osteotomy, and interlocking intramedullary nailing in right tibia to prevent pathologic fracture. These methods brought a good result of bone union and full weight bearing ambulation after 1 year and 6 month follow up. We think these methods are useful methods to control refracture and deformity, so we reported this case with bibliographic reviews.

• 대한골관절종양학회지
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• 제10권1호
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• pp.50-55
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• 2004

진행성 골화성 섬유이형성증은 매우 드문 유전적 질환이기는 하나 영유아 초기에 경부나 두부의 종괴에 동반하여 나타나는 특징적인 양측성의 족부 모지의 선천성 기형으로 진단이 가능하다. 그러나 오진으로 인한 잘못된 치료와 그로 인한 합병증이 병의 진행을 더 악화시킬 수 있으며 불필요한 처치를 행할 수 있어 처음 진단에 주의를 요하는 질환이다. 이에 저자는 이질환의 자연적 경과와 더불어 잘못된 치료로 인해 발생한 성인에서의 양상을 보고하는 바이다.

• 대한골관절종양학회지
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• 제7권4호
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• pp.157-161
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• 2001

비 호지킨 림프종은 약 1/4정도가 림프절외 조직에서 생기지만, 연부 조직에서 생기는 경우는 극히 드물다. 저자들은 좌측 액와부와 상완부에 피하 조직 종물의 형태로 발생한 비 호지킨 림프종 1례를 치험 하였다.

• 대한골관절종양학회지
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• 제18권2호
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• pp.109-112
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• 2012

뚜렛 외골증은 수부의 신전기전 아래 골막하 골이 매끈한 돔 형태로 피질 바깥으로 침착되는 것으로 대부분은 중위지골과 원위지골에 발생하는 것으로 알려져 있다. 이에 반해 거대한 뚜렛 외골증이 중수골에 생긴 매우 드문 증례를 경험하여 이를 보고하고자 한다.

• 대한골관절종양학회지
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• 제9권2호
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• pp.217-222
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• 2003

거대세포종은 주로 대퇴골 원위단, 경골 근위단, 요골 원위단등 장관골의 골간단부를 침범하여 팽창되는 골붕해성 병변을 일으키며 또한 그 치료 방법에 대해서도 골소파, 골소파 및 골이식 절제, 방사선조사, 절단, 한냉수술등 아직 특별한 원칙이 없는 상태이다. 본 교실에서 는 19세 남자의 슬개골에 발생한 거대세포종에 대해서 골 소파술후 자가골 이식술을 시행하였으며 이 결과를 문헌고찰과 함께 보고하는 바이다.

• 대한골관절종양학회지
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• 제5권4호
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• pp.229-234
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• 1999

Giant cell tumor of the talus is an extremely rare condition and therapeutic options are ill defined. Recently we experienced a case of giant cell tumor of the talar body in a 20-year-old male treated by curettage and bone graft. There was no recurrence at 1year follow-up. A case report and review of the literature are presented.

• 대한골관절종양학회지
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• 제5권4호
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• pp.216-220
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• 1999

The purpose of this study was to evaluate the role of c-fos oncogenes in the development of fibrous dysplasia and osteofibrous dysplasia. The immunohistochemical expression of c-fos protein was evaluated in 15 cases of fibrous dysplasia and 8 cases of osteofibrous dysplasia. Ten cases of fibrous dysplasia were weakly positive with c-fos. Six cases of osteofibrous dysplasia were weakly positive and the remaining two cases were strongly positive. The overall expression of c-fos protein is weaker than high-grade osteosarcoma, thus the implication of c-fos protein is little in the development of these tumors. Fibrous dysplasia and osteofibrous dysplasia share some features of characteristic histology and c-fos expression.

• 대한골관절종양학회지
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• 제4권2호
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• pp.94-98
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• 1998

Clear cell sarcoma of the kidney (CCSK) is a rare malignant tumor of the renal origin in childhood, distinguished from Wilms tumor by its pathologic and clinical features. Bone metastasis is one of the characteristic clinical features. The common site of metastasis of the clear cell Sarcoma of the kidney is axial skeleton including skull, spines, ribs and femur. A cases of clear cell Sarcoma of the kidney presented to us, which solely metastasized to the hand bones without metastasizing to any other tissues including axial skeleton. We report this case with review of literatures.

• 대한골관절종양학회지
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• 제13권2호
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• pp.152-156
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• 2007

Giant cell tumor of bone is relatively common neoplasm usually involving epiphysis of long bone. And rarely it involves the diaphysis or metaphysis without epiphyseal extension. We report on an 18-year-old girl with giant cell tumor of ulnar diaphysis. She was treated with wide excision and reconstuction with nonvascularized autogenous fibular graft. We harvested fibular fragment preserving fibular continuity to reduce donor site morbidity. Surgical outcome and functional result was excellent.

• 대한골관절종양학회지
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• 제4권1호
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• pp.59-64
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• 1998

Parosteal osteosarcoma is characterized as a densely ossifying lesion, usually occurring on the surface near the metaphyses of a long bone. The histological pattern is a well- differentiated mature bone trabeculae with a hypocellular spindle-cell stroma. The cytological details are those of a low-grade malignant lesion. The natural history of this lesion is indolent local growth, late invasion of the underlying bone, and infrequently, distant metastasis. However, there is a significant risk of eventual dedifferentiation into a high-grade lesion. We report here-a case of parosteal osteosarcoma dedifferentiated into a high-grade lesion, which occurred in the left distal femur of a 40-years-old woman, and discuss the experience in detail.