• 대한골관절종양학회지
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• 제6권1호
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• pp.22-29
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• 2000

목적 : 유골 골종의 치료에서 소파술 및 절제술을 이용한 치료 결과를 보고하고 영상증폭 장치하에 K-강선을 경피적으로 삽입후 핵을 Halo-mill로 제거하는 수술을 시행한 경우에도 양호한 결과를 얻어 치료법의 하나로 사료되어 보고한다. 대상 및 방법 : 1990년 3월부터 1998년 1월까지 유골 골종으로 진단하고 수술적 치료를 시행한 환자 20명을 대상으로 하였다. 남자가 14례, 여자가 6례였으며 연령분포는 7세부터 42세 까지 평균 20.8세였다. 추시기간은 최저 1년에서 최고 5년 6개월로 평균 3년 2개월이었다. 발생부위는 대퇴골이 9례로 가장 많았고, 경골이 6례, 척추 2례, 척골 1례, 상악골 1례 그리고 두개골이 1례였다. 대퇴골에 발생한 9례중 근위 골간단부는 5례, 경부가 2례, 그리고 골간부가 2례였다. 경골에 발생한 6례는 근위 골간단부와 원위 골간단부에 각각 1례 발생하고 나머지 4례는 골간부에 발생하였다. 정확한 진단과 병소를 찾아내기 위한 방사선학적 검사는 단순 방사선촬영, 골주사, 전산화 단층촬영과 자기공명영상을 이용하였다. 수술방법은 절제술과 소파술이외에 Halo-mill을 이용해 경피적으로 병소를 절제해 내는 방법을 사용하였다. 한편 척골에 발생한 1례의 경우에는 인공관절 전치환술을 시행하였다. 결과 : 단순 방사선촬영 소견상 골 경화의 중심부에 투명상을 나타내는 핵을 보이는 전형적인 소견을 보인 경우는 방사선 자료의 검토가 가능했던 15례중 10례였으며 나머지는 골피질의 경화소견만 보였다. 골주사는 14례에서 시행되었으며 전례에서 비정상적인 방사능 섭취의 증가가 나타났다. 전산화 단층촬영과 자기공명영상을 시행한 각 10례와 4례 중 병소를 확인하지 못한 경우는 전산화 단층촬영에서 1례가 있었다. 치료는 소파술 6례, 절제술 11례,Halo-mill을 사용한 경피적 절제술 2례, 그리고 인공 주관절 치환술 1례를 시행하였다. Halo-mill을 사용한 2례에서 모두 7mm 크기의 Halo-mill을 사용하여 절제술을 시행하였다. 추시 결과 모든 례에서 증상의 소실을 보였으며 재발한 경우는 없었다. 조직학적 소견상, 특징적인 병소를 확인하지 못하고 과골화 소견을 보인 1례를 제외하고는 모든 례에서 특징적인 병소를 확인하였다. 결론 : 유골 골종의 완치를 위해서는 병소를 완전히 제거하는 것이 중요한데 이를 위한 방법으로 보편적인 소파술이나 절제술이 사용될 수 있으나, 핵의 정확한 위치 및 크기가 확인되고 경피적으로 도달가능하며 Halo-mill로 핵을 제거할 수 있는 경우에는 Halo-mill을 이용한 경피적 병소 제거술의 사용이 가능할 것으로 사료된다.

• 대한세포병리학회지
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• 제1권1호
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• pp.98-102
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• 1990

Hepatoblastoma (HB) is a rare embryonic malignant tumor of the liver. Most morphological studies on HB have limited to the histological characteristics and only 3 cases of HB have been described in the cytology literature. We present 2 cases of HB occurring in children aged 1 year and 3 years, respectively. The distinctive cytologic features of fine needle aspiration of HB were clusters of tumor cells showing acinar and trabecular pattern, smaller tumor cells with a high nuclear-cytopalsmic ratio and hyperchromatic nuclei having prominent nucleoli, and the presence of extramedullary hematopoiesis and osteoid material. These features were also found in the cell block and the biopsy specimen, and appeared very useful in the differentiation of HB from hepatocellular carcinoma.

• 대한세포병리학회지
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• 제9권1호
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• pp.89-94
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• 1998

A case of fine needle aspiration cytology of an osteoclastic giant cell tumor of pancreas, which is an uncommon variant of ductal adenocarcinoma, is described. Aspirated tumor cells were characterized by three populations: (1) bland osteoclast like giant cells with multiple small, round nuclei with distinct nucleoli, and abundant cytoplasm, (2) Individually scattered or loosely clustered medium sized mononuclear tumor cells, having fine chromatin, smooth nuclear membrane, often prominent nucleoli, and high N/C ratio, (3) bland or atypical spindle shaped cells. Osteoid like lacy material was also seen on cell block section. The immunohistochemical studies using paraffin embedded cell block section showed positivities for vimentin and lysozyme in both giant and mononuclear turner cells. However, they were negative for cytokeratin, epithelial membrane antigen, S-100 protein, carcinoembryonic antigen, and p53.

• 한국임상수의학회지
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• 제20권2호
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• pp.259-262
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• 2003

A 13-year old male dog with right forelimb lameness, invisible swelling, anorexia and mild depression was referred to Veterinary leaching Hospital, College of Veterinary Medicine, Kyungpook National University. On forelimb radiographic views, periosteal and endosteal proliferation and cortical lysis and extremely aggressive and amorphous periosteal reactions were located along the metaphyseal region of the proximal humerus. Cytologic and histopathologic examinations after amputation showed anaplastic mesenchymal cells that produced osteoid changes, poorly differentiated osteoblast and osteoclast. And also, it included the neoplastic cells with large nucleoli, multiple nucleoli that differ in size and cytoplasm with several clear vacuoles. Based on the physical examination and laboratory, radiolographic, cytologic and histopathologic findings, this case was diagnosed as osteosarcoma of the proximal humerus.

• 한국임상수의학회지
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• 제33권1호
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• pp.48-50
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• 2016

A 10-year-old spayed female Maltese dog weighting 3.4 kg was referred with growing firm mass at the parietal bone region from 2 weeks ago. A firm, partially calcified mass ($1.9cm{\times}4.4cm$) was palpated in the region of the frontal and parietal skulls but had no neurologic signs. Computed tomography (CT) characteristics of mass were round to oval shape, fine granular appearance, and well defined margins. Mass involving the calvarial bones had invasion into the cranial vault with a significant intracranial portion. Histologically, the tumor was characterized by the presence of multiple lobules containing osteoid or cartilage in the center that were separated by anastomosing fibrous septae. This is case report described the clinical and histopathological features of multilobular tumor of skull in a Maltese dog.

• 대한수의학회지
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• 제53권1호
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• pp.61-64
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• 2013

A ten-year-old dog was presented with pancreatitis and increased hepatic enzymes. On necropsy a large firm mass was observed in the liver extending to the gall bladder. Smaller masses with similar texture were found in multiple organs including lung, stomach, pancreas, lymph nodes, omentum, and mesentery. Neoplastic cells were spindle shaped with prominent osteoid production and occasional trabeculae of woven bone. Tumor cell emboli were observed in the blood vessels and lymphatics of the omentum and stomach. Hepatic osteosarcoma with systemic metastasis is very rare and may serve to broaden the diagnostic spectrum of hepatic and pancreatic diseases in dogs.

• 치과방사선
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• 제26권2호
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• pp.175-180
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• 1996

Osteosarcoma is the most common malignant tumor of bone. The mean age of occurrence of osteosarcoma in the jaws is around 30, somewhat older than for other sites in the body. These lesions occur about equally in the maxilla and mandible. They most frequently develop in the body in the mandible, and the antrum and the posterior portion of alveolar ridge in the maxilla. We report a case of osteosarcoma in 35 years old female complaining swelling of the left cheek. Radiographic features showed cotton wool appearance in upper left posterior area. Histopathologic findings exhibited pleomorphic malignant osteoblasts and neoplastic osteoid.

• 대한족부족관절학회지
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• 제6권2호
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• pp.233-237
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• 2002

Osteogenic sarcoma is the most common primary malignant tumor of bone in which tumor cells form neoplastic osteoid or bone or both. Classic osteogenic sarcoma usually involves the metaphysis of the more rapidly growing long bones (distal femur, proximal tibia). Osteogenic sarcoma of the foot is rarely noted and only a few well documented cases have been reported. Osteogenic sarcoma of foot can clinically, radiographically, and histologically mimic several benign lesions and tumor-like lesions, so it sometimes leads to late diagnosis and delayed treatment. We experienced a case of primary osteogenic sarcoma on left calcaneus in 66-years-old female and report it with a review of references.

• 대한치과의사협회지
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• 제22권4호통권179호
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• pp.333-338
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• 1984

This is to report a case of traumatic bone cyst which occurred in the left condylar head of the mandible. It is a very rare case and the prognosis after operation seems to be fair, therefore we report as follows. 1. The pt, a 49 year-old female, has been suffering from difficulties of mastication with disfiguration of face due to deviation of mandible to the right side for 20 years. 2. Histopathologic findings showed the figure of multilocular bony cysts contained with fibrous tissue, osteoid tissue and many hematopoietic cells 3. Roentgenographic features showed well circumscribed radiolucent lesion with some radiopaque area. 4. After clinical evaluation, condylectomy was done to remove the lesion. 5. After the operation, the esthetic problem and masticatory functions were improved.

• Journal of Chest Surgery
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• 제52권4호
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• pp.243-246
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• 2019

Extraskeletal osteosarcoma (ESOS) is a malignant soft tissue neoplasm producing osteoid, without any continuity with the bone or periosteum. Primary ESOS presenting in the mediastinum is an extremely rare, yet aggressive malignant tumor associated with a poor prognosis. We report a case of primary ESOS arising from the thymus in a 63-year-old male patient.