• Tuberculosis and Respiratory Diseases
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• 제48권3호
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• pp.388-393
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• 2000

저자들은 우측 흉통과 기침을 주소로 내원한 57세 남자환자에서 우측 폐하부에 $12{\times}8cm$ 가량의 종괴를 단순 흉부 X-선 촬영과 흉부 CT 촬영등으로 진단후 좌측 개흉술로 치료한 국소성 섬유성 종양을 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• Journal of Chest Surgery
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• 제20권3호
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• pp.593-597
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• 1987

Mesothelioma is a primary tumor of the pleura. There are two forms of mesotheliomas; diffuse form and localized form. The majority of localized mesotheliomas are benign, but the tumor with pedicle recur at 20% after removal of it. Malignant localized fibrous mesothelioma is differential diagnosed pathologically and clinically with diffuse mesothelioma. Symptoms of localized mesothelioma are generally related to the size of the tumor. We presented one case of malignant localized fibrous mesothelioma. The patient was 32 years old female and chief complaints were dyspnea and dry cough. Sputum cytology and needle lung biopsy were not able to diagnose definitely the tumor. Explothoracotomy was carried out for definite tissue biopsy. At the time of operation, huge adult head size mass was in the right thoracic cavity. The surface of the mass was nodular, multilobular and had hard consistency. Pedicle was formed above first rib and its diameter was 4.5cm. There was no adhesion except to RUL. Frozen biopsy suggested mesothelioma. Extirpation of the mass, right upper lobectomy. and partial pleurectomy were carried out.

• Journal of Chest Surgery
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• 제30권3호
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• pp.353-353
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• 1997

흉막에 발생하는국소성 섬유성 종양은 드문 질환으로 대부분의 경우 단순흉부촬영상 우연히 발견되며 특징적 인 임상상 및 조직병 리학적 소견을 보인다. 본 논문에서는 증상없는 저혈당을 동반한 악성 국소성 섬유성 종양 1례 및 양성 국소성 섬유성 종양 2례를 보고하고자 한다. 악성의 예에서는 개흉술을 통해 종양을 절제해 내었고 수술직후 저혈당의 소실을 관찰할 수 있었으며 양성 2예에서는 비디고 흉강경을 이용하여 종양을 절제할 수 있었다.

• Journal of Chest Surgery
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• 제30권3호
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• pp.253.2-356
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• 1997

흉막에 발생하는국소성 섬유성 종양은 드문 질환으로 대부분의 경우 단순흉부촬영상 우연히 발견되며 특징적 인 임상상 및 조직병 리학적 소견을 보인다. 본 논문에서는 증상없는 저혈당을 동반한 악성 국소성 섬유성 종양 1례 및 양성 국소성 섬유성 종양 2례를 보고하고자 한다. 악성의 예에서는 개흉술을 통해 종양을 절제해 내었고 수술직후 저혈당의 소실을 관찰할 수 있었으며 양성 2예에서는 비디고 흉강경을 이용하여 종양을 절제할 수 있었다.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제34권6호
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• pp.649-652
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• 2008

Osteoblastoma is a relatively rare benign bone tumor representing less than 1% of all bone tumors. The tumor usually involves the spine and sacrum of young individuals, less than 10% being localized to the skull, and nearly half of these affect the mandible, especially the posterior segments. In clinical finding, osteoblastoma present mainly with pain, swelling, and expansion of bone cortex. Radiographic appearances are variable, but frequently a well-delineated radiolucent lesion containing varying amounts of mineral deposits is seen. Histologically, ostoeblastoma is consists of irregular trabeculeae of osteoid and immature bone present within highly vascular connective tissue matrix. Osteoblastoma must be differentiated from a number of bone-producing lesions, including osteoid osteoma, fibrous dysplasia, ossifying fibroma, fibrous dysplasia, and osteosarcoma. If diagnosis may be mistaken for osteosarcoma, there are risks of more aggressive and irreversible treatment. Differential diagnosis of osteoblastoma is important. The preferred treatment of osteoblastoma is conservative approach and surgical excision. Recurrence following surgical intervention is rare. We treated osteoblastoma located in premolar area of mandible by excision with preservation of vital structure, such as nerves and teeth. So we report our clinical treatment with literature review

• 대한골관절종양학회지
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• 제1권2호
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• pp.240-243
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• 1995

본 저자들은 희귀 증례로 사료되는 주상골에 발생한 유골 골종 1 례를 치험하였기에 보고하며, 유골 골종의 특징적인 임상적, 방사선학적 소견으로 인하여 진단은 어렵지 않았으며, 치료는 구역 절제술(en bloc excision)이 원칙이나, 주상골에 발생한 유골 골종의 경우는 광범위 소파술과 자가골 이식술을 통하여 재발없이 종양의 완전 치유가 가능하였던 것으로 사료된다.

• Journal of Chest Surgery
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• 제18권1호
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• pp.69-74
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• 1985

Most clinicians have taken a lot of interest in tumors arising from the bony thorax because not only of their rarity and predictable diagnosis which could be reflected as a unique radiologic shadow but also variable surgical modes for maintenance of chest wall stability encountered after en-bloc resection. By the retrospective review, we have analyzed 24 cases of primary bony thorax tumors which were experienced and surgically treated at the St. Mary`s hospital of Catholic Medical College from Jan. 1969 to Sept. 1984. The results are as follows: 1. Age incidence was evenly distributed through all decades and the male-female ratio is 15:9. 2. 16 cases out of 24 were benign tumors and the commonest one of which was fibrous dysplasia. 3. Remaining 8 cases were malignant tumors and among which osteogenic sarcoma was the commonest one. 4. The majority of tumors [22/24] were developed from the rib and the remains were from the sternum. 5. Common manifestation were palpable mass or swelling and localized tenderness. 6. Various kinds of operative procedure were underwent: single resection of rib including tumor,14 cases; multiple resection of ribs with chemotherapy or myoplasty, 2 cases; en-bloc resection of the chest wall and reconstructive procedure, 5 cases; partial resection of sternum, 1 case; bone biopsy and chemotherapy, 2 cases.