• Tuberculosis and Respiratory Diseases
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• 제57권4호
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• pp.368-371
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• 2004

저자들은 기침을 주소로 내원하여 우측 종격동 종괴로 인한 상대정맥증후군을 보였으며 비디오 흉강경을 이용한 종괴의 조직검사와 조직에서의 항산균 도말검사 양성으로 결핵성 림프절염으로 진단하고 치료한 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• Journal of Chest Surgery
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• 제30권3호
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• pp.344-347
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• 1997

상대정맥 증후군을 가진 49세 여자환자에 spiral vein graft를 이웅한상대정맥 우회로 조성술을 실시 하여 좋은 결과를 얻었다. 이 복합 나선형 이식 편은 폐쇄된 상대정 맥을 우회하여 우측 무명동맥과 우심 이간에 이식되었다. 이식편은 환자 자신의 대복재정 맥을 세로로 절개하여 스탠트에 나선형으로 감은 후 정맥의 가장자리들을 봉합하여 하나의 큰직경을 가진 도관으로 만든 것이다. 환자는 증세 호전되었고 수술 후 21일째 합병증 없이 퇴원하였다.

• Journal of Chest Surgery
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• 제38권1호
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• pp.67-71
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• 2005

상대정맥증후군의 원인은 악성과 비악성 두 가지로 나눌 수 있다. 항암 화학요법이나 방사선 치료에 반응이 없는 악성 종양에 의한 상대정맥증후군의 경우, 수술보다는 방사선학적 중재적 시술로 치료하는 것이 일반적이다. 그러나 비악성 원인에 의한 경우 수술과 중재적 시술 중 어느 것이 우수한지 아직 정립되어 있지 않다. 저자들은 혈액 투석용 카테터에 의한 상대정맥증후군 환자 2명에 대해 수술적 치료를 시도하였다. 2명 모두 중재적 시술이 불가능하거나 실패한 경우였다. 첫 번째 환자는 expanded polytetrafluoroethylene를 이용하여 무명정맥-우심방 단락술을 시행하였고, 다른 한 환자는 혈전 제거술과 함께 자가 심막을 이용하여 상대정맥과 무명정맥의 첩포 확장술을 시행하였다. 두 환자 모두 증상의 현저한 호전이 있었으며, 수술 후 시행한 혈관 조영술에서 우회혈관의 현저한 저하가 관찰되었다.

• Tuberculosis and Respiratory Diseases
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• 제41권1호
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• pp.58-62
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• 1994

저자들은 폐렴간균 폐렴에 의한 우상엽의 용적 증가로 인하여 유발된 상대정맥 증후군 1예를 임상 경험한후 medline검색상 SVCS의 유발 원인으로서 폐렴간균 폐렴은 최초의 증례로 사료되므로 이에 보고하는 바이다.

• Journal of Chest Surgery
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• 제29권2호
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• pp.219-222
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• 1996

34세 남자가 복수 및 복부 팽 만감을 주소로 입원하였다. 단층촬영 및 하대정맥 조영술상 간정맥 직상부의 하대 정맥폐색이 의심되는 Budd-Chiari 증후군으로 진단되었다. 대증요법으로 간문맥고혈압과 하대정맥폐색증상이 호전이 안되어, 체외순환, 중등도저체온 및 정 상심박동하에 폐색부위절제술 및 하대정맥성형술을 10mm인조혈관을 사용하여 시행하였다. 술후 환자는 구강및 피부와 이학적 검사상 구강궤양, 피하 혈전성 정맥염, 모낭염성 병변, 피부의 자극성 항진 및 포도막염이 관찰되었고 상대정맥 폐색증상이 병발하였으며 Behcet씨 병으로 진단되었다.

• Journal of Chest Surgery
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• 제23권1호
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• pp.162-168
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• 1990

Unroofed coronary sinus syndrome is an uncommon anomaly which is caused by incomplete formation of the left atriovenous fold and it is usually associated with persistent left superior vena cava. It may be diagnosed by cardiac catheterization and cineangiography but, if it is not diagnosed, it can bring out significant complications due to right to left shunt, such as brain abscess, cerebral embolism, transient ischemic attack, arterial desaturation and there will reduced patient`s life expectancy. Therefore corrective operation was needed. A case of unroofed coronary sinus syndrome which combines with valvular heart disease was experienced at the department of thoracic & cardiovascular surgery of Kosin medical college. The patient was 49 years old female and she complained dyspnea on exertion for 2 yrs. Cardiac catheterization with cineangiography and both superior venacavogram were performed for diagnosis and she was diagnosed as unroofed coronary sinus syndrome combined with mitral and tricuspid regurgitation. Surgical correction was accomplished by reroofing of coronary sinus with pericardial patch, closure of atrial septal defect and annuloplasty of both atrioventricular valves. Postoperative results were satisfactory and course of recovery was uneventful. We report a case of unroofed coronary sinus syndrome with review.

• Journal of Yeungnam Medical Science
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• 제7권2호
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• pp.151-158
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• 1990

We reviewed 30 cases of superior vena cava syndrome in adult patients who were seen at the Yeungnam University Hospital from January 1985 to June 1990. The results were as follows : 1. The male-to-female ratio was 6.5:1, and the most patients were in the age group between the sixth and seventh decades. 2. The most common symptoms were dyspnea (87%) and followed by cough (63%), facial swelling (63%) and chest pain (44%) and the physical signs were dilated neck vein (97%), facial edema (93%) and facial flushing (45%) in order of frequency. 3. The simple chest x-ray findings were superior mediastinal widening (90%), right hilar mass (77%) and pleural effusion (31%). 4. Diagnosis was made by history and physical examination (100%), chest C-T scan (100%), simple chest x-ray (97%), bronchoscopy with biopsy (40%) and so on. 5. 21 cases of patients were confirmed by histology : 14 cases (46%) of bronchogenic ca. 4 cases (14%) of lymphoma, 3 cases (10%) of metastic lung ca. Of bronchogenic ca. small cell ca was 7 cases (23%), squamous cell ca, 5 cases (17%), and unclassified ca was 2 cases (6%). 6. In response of treatment, the clinical improvement was achieved in 18 cases with radiotherapy alone. 1 case with chemotherapy only, and 6 cases with radio-chemotherapy.

• Clinics in Shoulder and Elbow
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• 제18권1호
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• pp.43-46
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• 2015

Pancoast syndrome (PS) is characterized by a malignant neoplasm of the superior sulcus of the lung with destructive lesions of the thoracic inlet and involvement of the brachial plexus and cervical sympathetic nerves. The most common initial symptom of PS is shoulder pain; however, cough, dyspnea, and hemoptysis, signs often associated with lung cancer, are not as common. Investigation of PS can be difficult even with plain radiographs of the chest because it is surrounded by osseous structures such as the ribs, vertebral bodies, and manubrium. Due to these characteristics, orthopedic surgeons tend to make a misdiagnosis resulting in delay of appropriate treatment. Here we report on a patient who was supposed to undergo rotator cuff repair for his shoulder pain and weakness, and was eventually diagnosed with PS.

• Tuberculosis and Respiratory Diseases
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• 제78권3호
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• pp.289-292
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• 2015

Lemierre syndrome (LS) is a septic thrombophlebitis of the internal jugular vein (IJV) following an oropharyngeal infection. LS is commonly caused by normal anaerobic flora and treated with appropriate antibiotics and anticoagulation therapy. Although the incidence of disease is very rare, 15% cases of LS are fatal even in the antibiotic era because of disseminated septic thromboemboli. We reported a case of extensive bilateral LS due to methicillin-resistant Staphylococcus epidermidis in a 63-year-old female with lung adenocarcinoma. Initial examination revealed a retropharyngeal abscess; hence, intravenous ceftriaxone and steroid were initiated empirically. However, pulmonary thromboembolism developed and methicillin-resistant S. epidermidis was identified in the bacterial culture. Despite intensive antibiotic and anticoagulation therapies, extensive septic thrombophlebitis involving the bilateral IJV and superior vena cava developed. Adjunctive catheter-directed thrombolysis and superior vena cava stenting were performed and the patient received antibiotic therapy for an additional 4 weeks, resulting in complete recovery.

• Journal of Chest Surgery
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• 제27권4호
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• pp.335-338
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• 1994

Traumatic asphyxia is a distinctive clinical syndrome characterized by cervicofacial cyanosis and edema, bilateral subconjuctival hemorrhage, and multiple petechiae of the face, neck, and upper part of the chest after a severe compressive crush injury of the thorax or of the upper part of the abdomen.The pathophysiologic mechanism of traumatic asphyxia is reflux of blood from the heart retrograde through the valveless superior vena cava and the great veins of the head and neck by severe compression of the thorax or the abdomen.We experienced one case of the traumatic asphyxia, and its clinical features are discussed.