• 한국임상수의학회지
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• 제17권1호
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• pp.252-255
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• 2000

A 13.5kg, 15-year-old male mongrel dog with anemia, anorexia, vomiting and abdominal distension was referred to the Veterinary Medical Center of the Tokyo University. Radiographic and ultrasonographic findings indicated primary splenic tumor. The tumor was located at body of the spleen, which was surgically removed by splenectomy. Histopathological examination of the mass revealed sarcoma type tumor derived from the mesenchymal origin. The patient was in good health after surgery but suddenly showed abdominal distension on the 3 months after. Radiographic findings indicated abdominal neoplasms. The 2nd operation was performed and removed the recurrent mast but suddenly died on the 4th day. Histopathological examination of the tumor was myxosarcoma.

• 한국임상수의학회:학술대회논문집
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• 한국임상수의학회 2009년도 춘계학술대회
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• pp.253-253
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• 2009

• Journal of Chest Surgery
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• 제34권11호
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• pp.861-864
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• 2001

원발성 심장 점액육종은 대단히 희귀하며 원발성 심장 종양 중에서도 드물다. 저자들은 희귀한 원발성 심장 점액육종을 보고하는 바이다. 환자는 40세 여자 환자로 운동시 호흡 곤란과 심계 항진을 주소로 내원하였다. 심초음파 검사로 좌심방내 종양이 발견되어 응급 수술을 시행하였다. 좌심방내의 고식적 종양 절제후 병리 소견상 심장 점액 육종으로 진단되었으며 수술 후 별다른 합병증 없이 퇴원하였다.

• 한국임상수의학회지
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• 제29권2호
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• pp.173-176
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• 2012

6 년령의 수컷 시츄 견이 복부 팽만을 주 호소로 내원하였다. 복부 방사선 검사와 초음파 검사에서 많은 양의 액체를 포함하고 있는 연부조직 밀도의 종괴가 발견되었다. 종괴의 세포학적 검사를 위해 초음파 유도 세침흡인을 실시하였으며, 세포학적 검사 결과 섬유화가 동반된 육아조직이 의심되었다. 종괴의 확인과 수술적 제거를 위해 진단적 개복술을 실시하였다. 개복시 원위 공장부위에 인접한 장간막의 뿌리에서 유래한 종괴가 확인되었고 종괴는 원위공장 부위에 부착되어 있었다. 종괴와 부착 부위의 분리가 어려웠기 때문에 종괴와 부착 부위를 모두 수술적으로 제거하였으며 장문합술을 실시하였다. 종괴의 조직병리학적 검사 결과 저 악성도 점액육종이 진단되었으며, 종양 세포는 알시안 블루 염색에 양성 반응을 보였다. 추가로 실시한 Ki67 항체를 이용한 면역조직화학 염색 결과 Ki-67 지수는 2.5 였다. 환축은 절제술 실시 후 현재까지 30개월 동안 전이와 재발의 증거 없이 살고 있다.

• Journal of Chest Surgery
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• 제7권1호
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• pp.61-66
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• 1974

Primary tumors of the chest wall are rare than those of other portions of the body. Soft tissue tumors of the chest wall, though these are benign or malignant, should not be paid special attentions about their management than other soft tissue tumors of the body. Thoracic skeletal tumors, however, have some problems in the treatment because of defect in chest wall leading to herniation of lung and paradoxical movement of thoracic cage. The authors experienced 10 case of primary chest wall tumors at the department of thoracic and cardiovascular surgery, the national medical center, during last 15 years. Five of 10 cases were soft tissue tumors, and they were 2 case of lipoma and each one case of myxosarcoma and leiomyosarcoma. Among 5 bone tumors there no cases of sternal tumor, and their histopathological diagnosis were each one of fibrous dysplasia, giant cell tumor, osteochondroma, Ewing`s sarcoma and osteogenic sarcoma. Wide excision, though it was palliative one in certain case, was performed in 9 cases and only diagnostic incisional biopsy in one case, There were no postoperative deaths during admission to the hospital and all cases were missed during short term follow up after discharge from the hospital.

• Tuberculosis and Respiratory Diseases
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• 제46권1호
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• pp.129-135
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• 1999

We describe unusual manifestations of congenital cystic adenomatoid malformation (C.C.A.M.) of the lung, such as movable fungal ball-like intracystic blood clots and hemoptysis, which were detected in previously healthy 23 years-old woman. We identified blood clots only after left upper lobectomy and could not distinguish from fungal ball with radiographic methods. CCAM of the lung, rare and lethal form of congenital pulmonary cystic disease, was initially introduced by Ch, in and Tang in 1949. The histogenesis of this lesion is characterized by polypoid glandular tissue proliferation and overgrowth of mesenchymal elements due to cessation of bronchiolar maturation which occurred in after 16weeks intrauterine period. In 80-95% of reported cases, the lesion was confined to a single lobe and there was no lobe and right and left lung predilection The clinical presentation may be widely variable, ranging from intrauterine fetal death to late discovery in childhood with recurrent pulmonary infection. But there,s no reports which were misdiagnosed with intracystic fungal ball. The treatment choice is lobectomy of affected lobe. There,s a few case reports with rhabdomyosarcoma, bronchiolar cell carcinoma and myxosarcoma arising in CCAM patients. Therefore, early resection is recommended even if asymtomatic cases. We experienced a rare case of CCAM of the lung in 23 years old female, and there were intracystic fungal ball-like movable blood clots in lower portion of left lung. After left upper lobectomy was performed, now she is discharged and followed up without any complications.