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A Case Report of Adenoid Cystic Carcinoma in Trachea (기관에 생긴 선양낭포암 치험 1례)

  • 전희재
    • Journal of Chest Surgery
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    • v.26 no.6
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    • pp.501-504
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    • 1993
  • Adenoid cystic carcinoma of the tracea is rare, but is a very serious critical life-threatening disease.Nearly all the lesions of the trachea are presented as obstructive lesions. Bronchoscopic examination including chest CT, tomogram and air tracheogram are essential for the further definition of these lesions. This is a case report of adenoid cystic carcinoma in a 47 years old male patient. The tumor was located in cervical trachea with wide base and obstructing the lumen almost completely. The patient`s symptom was productive cough and hoarseness for 4 months. The tumor was resected and End-to-End anastomosed. The tumor was confirmed to be adenoid cystic carcinoma histopathologically. The need for removal of tracheal tumor whether complete or incomplete, is clear enough regardless of the histology of the tumor. This patient was treated post-operatively with radiation.

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Infradiaphragmatic Retroperitoneal Pulmonary Sequestration - A Case Report - (횡격막하 후복막강에 발생한 폐격리증 - 1례 보고 -)

  • Hur, Jin;Goo, Bon-Won
    • Journal of Chest Surgery
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    • v.35 no.3
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    • pp.244-247
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    • 2002
  • Pulmonary sequestration is a very rare congenital malfomation, especially when it is located in the infradiaphragmatic retroperitoneal space. The patient was a 56-year-old man with no respiratory symptom but had some postprandial epigastric discomfort for several days. Plain chest x-ray revealed mild elevation of left diaphragm and abdominal CT scan showed large cystic retroperitoneal mass with some calcification. We performed the operation through the thorachoabdominal incision and the mass was proven to be a pulmonary sequestration. Therefore, we report the case with review of literatures.

Fast DRR generation for real-time registration (실시간 정합을 위한 고속 DRR 영상 생성)

  • Park, Seong-Jin;Kim, Kye-Hyun;Hong, Helen
    • Proceedings of the Korean Information Science Society Conference
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    • 2005.07a
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    • pp.697-699
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    • 2005
  • 본 논문에서는 그래픽 하드웨어를 이용한 텍스처기반 볼륨렌더링으로 DRR 영상을 고속으로 생성하는 방법을 제안한다. 제안방법은 크게 세단계로 구성된다. 첫째, CT 영상 슬라이스 데이터에서 각 슬라이스를 최인접보간법으로 보간함으로써 등방해상도의 볼륨데이터를 생성한다. 둘째, 그래픽 하드웨어의 메모리용량 때문에 발생하는 문제를 해결하기 위해 텍스처 메모리의 효율적 관리방법을 제시한다. 셋째, 텍스처기반 볼륨렌더링을 이용해서 X-ray 영상과 유사한 투시투영한 DRR 영상을 생성한다. 본 논문에서 제안한 방법을 평가하기 위해서 인공 심장 데이터를 사용한다. 제안방법의 수행시간과 화질을 평가하기 위해서 기존 광선추적법, 복셀투영법을 적용한 DRR 영상과 비교 분석하였다. 실험결과 제안 방법은 기존 방법에 비해서 빠르게 DRR 영상을 생성하였고, 영상의 화질 또한 광선추적법의 결과 영상의 화질만큼 좋은 영상을 생성하였기 때문에 실시간 정합에 적합하였다.

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Mediastinal lipoma and liposarcoma (종격동 지방종 및 지방육종: 3례 보고)

  • Kim, Won-Gon;Kim, Ju-Hyeon
    • Journal of Chest Surgery
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    • v.16 no.3
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    • pp.375-380
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    • 1983
  • The lipomatous of the mediastinum are fairly uncommon tumors. Since 1971, two patients with proven mediastinal lipoma and one primary liposarcoma of the mediastinum have been treated at the Seoul National University Hospital. This report reviews our experience with the review of literature. Case 1.: A 3 year old body revealed a huge round homogenous mass density in the posterior mediastinum in routine chest X-ray. The tumor mass, lipoma, was successfully removed and postoperative course was uneventful. Cases 2.: An asymptomatic 24 year old male was operated on with the preoperative diagnosis of mediastinal lipoma. His preoperative chest X-ray and CT films showed a huge anterior to middle mediastinal tumor, right, with fat density. There is no postoperative problem after successful removal of the tumor mass. Case 3. : A 24 year old female was hospitalized with the complaints of cough and chest pain. A mediastinal mass was removed, which proved to be a liposarcoma on pathologic examination. About one year later, she was found to have recurrent liposarcoma in the right chest area at the OPD follow-up. She was lost to follow-up since then.

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"DUMBBELL" Neurilemmoma -1 case Report- (DUMBBELL 신경종양 -1례 보고-)

  • 박영환
    • Journal of Chest Surgery
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    • v.23 no.3
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    • pp.556-560
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    • 1990
  • A 22 year old soldier was discovered on routine study for discharge to have a mass in the posterior mediastinum He was admitted due to high fever and improved by antibiotic treatment for 2 weeks. Chest PA, apicogram, myelogram and CT scan demonstrated enlargement of the neural foramen at the T1 level with erosion of the posterior aspect of the vertebral body and the pedicle contiguous with the intrathoracic mass, A myelogram showed a large extradural defect at the T1 level on the left. There were no clinical signs of cord compression. A standard posterolateral thoracotomy incision was made with extension to high thoracic vertebra. The 3rd rib was resected and the angles of the posterior portion of 1st and 2nd ribs were cut and rib heads were removed. Extrapleural neurilemmoma 6x6 cm was resected intrathoracically. And after removal of the pedicle and the lamina, intraspinal extradural mass 3 X 2 cm was resected carefully with trivial tearing of the dura which was sealed with gel-foam and pleura. There was ma postoperative neurological complication.

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THYMOLIPOMA(Report of one case) (흉선지방종-1례 보고-)

  • 백승환
    • Journal of Chest Surgery
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    • v.23 no.3
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    • pp.561-565
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    • 1990
  • We experienced thymolipoma which is a rare benign mediastinal tumor, an admixture of atrophic thymic tissue and matured adipose tissue. The patient was, 13 years old boy, admitted due to anterior mediastinal mass on routine chest X-ray and complained of mild exertional dyspnea. The physical examination revealed percussion dullness, decreased breathing sound at right anterior hemithorax. The chest PA and lateral views showed both paracardiac mass density and obliteration of retrosternal clear space. The chest CT Scan showed tubular structure containing of thymic tissue and enhanced fatty tissue, suggested thymolipoma. Operation was performed under the impression of thymolipoma. Through median sternotomy, the huge mass was resected. Grossly, the mass was yellowish fatty colored, measured 15X12X10cm, weighed 600gm. Light microscopic examination showed that thymic tissue containing of Hassal`s corpuscles were surrounded by matured adipose tissue, as the characteristic finding of thymolipoma. The postoperative course was uneventful.

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Tracheobronchial Rupture following Blunt Chest Trauma -1 case report- (외상성 기관지 파열 -1례 보고-)

  • 김용한
    • Journal of Chest Surgery
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    • v.23 no.3
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    • pp.588-593
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    • 1990
  • The rupture of tracheobronchial tree caused by non penetrating blunt trauma is being increased in incidence though it is still rarely occurred on now Because this type of injury is uncommon, a high index of suspicion should be maintained in all crush injuries involving the chest. Early diagnosis and primary repair not only restore normal lung function but also avoid the difficulties and complications associated with delayed diagnosis and repair. We experienced a case of tracheobronchial rupture caused by non penetrating blunt chest trauma without rib fracture. The patient was a 16 year old male who was a high school student. He was compressed on anterior chest by hand ball goal post being failed down on the morning of admission day. After this accident, he was suffered from progressively developing dyspnea and subcutaneous emphysema on face, neck and anterior chest. The diagnosis, tracheal rupture, was made by chest CT and bronchoscopy. After right thoracotomy, the ruptured site was directly closed by using interrupted suture. Post-operative course was uneventful. Thus we report this case of traumatic tracheal rupture with review of literature.

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"DUMBBELL" Neurilemmoma -A Case Report- ("DUMBBELL" 신경종양 -1례 보고-)

  • Park, Jin-Seok;Im, Seung-Pyeong;Kim, Gwan-Tae
    • Journal of Chest Surgery
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    • v.27 no.6
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    • pp.502-505
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    • 1994
  • Neurogenic tumors of the mediastinum may have an intraspinal component connected by a narrowed segment of tumor in the intervertebral foramen,hence the descriptive term dumbbell.Recently we had an occasion to remove a dumbbell neurilemmoma in a 62 years old woman using an approach designed to allow wide posterolateral thoracotomy and concomitant laminectomy for a single stage removal of the entire tumor. The mass in the posterior mediastinum was discovered on routine chest roentgenography. CT scan demonstrated a dumbbell shaped soft tissue mass density compressing spinal canal but preserving spinal cord. There were no neurologic signs. A standard posterolateral thoracotomy incision was made to remove tumor mass and then T5 unilateral laminectomy has done by Neurosurgeon. 7 x 7 cm sized extrapleural neurilemmoma was round, cystic, soft mass which covered parietal pleural with invaded regional vertebrae. There was no postoperative neurological complication.

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Endodermal Sinus Tumor of the Mediastinum[Yolk Sac Tumor] - A Case Report - (종격동에 발생한 내배엽 동종[난황난종]: 1례 보고)

  • 이성열
    • Journal of Chest Surgery
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    • v.25 no.5
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    • pp.555-561
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    • 1992
  • Endodermal sinus tumor[EST] of the mediastinum is a rare germ cell neoplasm. It usually arises from the ovaries and testes but also arises from multiple extragonadal site including the mediastinum. Characteristically, alpha feto protein level is high and used for monitoring the clinical course. EST of the mediastinum is poor prognosis because of its direct invasion. The patient was 18 month old female with chief complaints of cough and fever. In the chest X-ray and CT, large encapsulated, 7x6cm sized, mass of anterior med-iastinum was found, and we could excise it completely because it was well encapsulated and not invaded but only adhered to aortic arch, pericardium and left upper lung. And confirmed it as EST by histopathology. Pre-operative alpha feto protein[AFP] level as 41,748ng/ml and decreased to 2, 663ng /ml at 14th postoperative day, 644ng /ml at 31th postoperative day. From 17th post-operative day, chemotherapy was started and keep going now.

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Bilateral Mediastinal Lymphangiohemangiomas Containing Anomalous Venous Components - A case report -

  • Bae, Chi-Hoon;Jung, Kyung-Jae
    • Journal of Chest Surgery
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    • v.44 no.5
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    • pp.373-376
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    • 2011
  • Lymphangiohemangiomas of the mediastinum are exceedingly rare and few cases have been published in the English literature. This report may be the only reported case in which lymphangiohemangiomas were found bilaterally. We report a case of a 7-year-old boy with an incidental finding of an abnormal mediastinal shadow on a chest X-ray. The chest CT showed a large mass in the left superior mediastinum and another in the right posterior mediastinum. The left mass had anomalous venous channels connected to the left innominate vein, and the right mass to the left atrium. We performed an excision of the mass in the left side first and then the right side one month later. Anomalous venous channels were dissected carefully and ligated. There were no complications and no signs of recurrence 30 months after the operation.