• Journal of Chest Surgery
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• 제12권2호
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• pp.140-144
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• 1979

This is a report of a case of superior vena caval syndrome due to idiopathic mediastinal fibrosis, which was surgically treated. The patient was 35-year-old Korean male who progressively complained shortness of breath about for 40 days prior to operation. Phlebogram of SVC showed indentation of SVC at the site of cavoatrial junction. The operation was performed under impression of bronchogenic cancer of right hilum. After thoracotomy, it was found a irregular mass in the mediastinum at the level of cavoatrial junction, which was developed to surrounding with SVC, pericardium, trachea and bronchus and they fixed together to immobile. Bypass graft between SVC and right atrial appendage was performed using a pericardial roll tube This is a report of a case of superior vena caval syndrome due to idiopathic mediastinal fibrosis, which was surgically treated. The patient was 35-year-old Korean male who progressively complained shortness of breath about for 40 days prior to operation. Phlebogram of SVC showed indentation of SVC at the site of cavoatrial junction. The operation was performed under impression of bronchogenic cancer of right hilum. After thoracotomy, it was found a irregular mass in the mediastinum at the level of cavoatrial junction, which was developed to surrounding with SVC, pericardium, trachea and bronchus and they fixed together to immobile. Bypass graft between SVC and right atrial appendage was performed using a pericardial roll tube [$1.3{\times}5$ cm]. After that SVC was decompressed very well. SVC pressure was markedly reduced from 32 cm $H_2O$ in preoperative to 21 cm $H_2O$in postoperative. Mediastinal fibrosis was confirmed by histopathological examination postoperatively. The postoperative course was uneventful.

• Journal of Yeungnam Medical Science
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• 제29권1호
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• pp.38-41
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• 2012

Behcet's disease is a rare multisystemic disorder whose main pathological defectis vasculitis, and superior vena cava (SVC) syndrome without thrombosis is a very rare manifestation of the disease. These authors encountered a case of SVC syndrome without thrombosis caused by Behcet's disease. A 33-year-old man visited the hospital for aggravated dyspnea without any related medical and familial history. He had a threeday history of abrupt swelling of the face, neck, and right arm. He suffered from recurrent oral ulcer, and there were acneiform nodules on his face as well as redness and swelling at the site of the intravenous injection. On the multi-detected computed tomography (CT) chest angiograms (chest angio MDCT), the SVC narrowed without thrombosis. Venogram was carried out, and percutaneous transluminal balloon angioplasty of the SVC stenotic site was performed. The following day, the swelling was found to have subsided. The details of the case are reported herein.

• Journal of Chest Surgery
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• 제35권3호
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• pp.235-238
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• 2002

상대정맥 증후군을 유발하는 여러 가지 원인들 중에 상대정맥 자체에서 발생하는 종양은 매우 드물다. 저자들은 상대정맥에 발생하여 혈류 장애를 초래한 평활근육종 1례를 수술 치료 하고 추적 관찰하여 보고하는 바이다. 환자는 39세 여자 환자로 내원 전 6주 동안의 안면 부종 및 두통을 주소로 내원하였다. 내원 시 안면 부종과 더불어 경부 및 상지의 정맥 충혈을 보였고, 중심정맥압은 측정 치 않았으나 경부 및 상부 흉벽의 측부혈행로도 보였다 단순 흉부 사진 상 우상부 종격동의 연부조직 종괴의 음영을 확인하고 흉부 전산화 단층 촬영 및 상대정맥 조영술을 시행하여 혈류장애를 초래하고 있는 커다란 종괴를 확인하였다. 수술은 흉골 정중 절개를 통해 체외 순환의 도움 하에 상대정맥을 종절개 하였다. 종양은 무명정맥입구에서 시작해서 우심방-상대적맥 접합부 약 1-2cm 우심방 안까지 위치하고 있었다. 먼저 종괴를 제거한 후 우경정맥의 혈전은 풍선 카테타를 이용하여 완전히 제거하였다. 조직검사상 상대정맥에서 발생한 평활근육종을 진단하였고, 수술 후 14개월 추적 관찰하는 중에 별다른 문제는 없었으며, 상대정맥 조영에서도 정상적인 소견을 보였다.

• Journal of Chest Surgery
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• 제35권3호
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• pp.239-243
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• 2002

본 증례의 39세 남자는 전신부종과 간부전증을 일으키는 Budd-Chiari syndrome과 상대정맥 폐색증을 가지고 입원하였다. 보존적 내과 치료 후 방사선과의 침습적 방법에 의한 확장술에 실패하여 하공정맥-우심방 단락술을 시행하였다. 수술은 정중흉골 절제술 및 직사행 복부 절제술을 통하여 직경 24 mm의 Dacron graft를 사용하여 좌신정맥 하에서 하공정맥-우심방 단락술을 체외순환을 하지 않고 시행하였다 수술후 출혈이나 합병증없이 양호한 결과를 보였으며 수술당일부터 항응고제 치료를 병행하였다. 술후 26일째 시행한 복부 도플러 초음파 상에서 graft의 유통성이 양호함을 확인하였다. 퇴원시 상대정맥 폐색 증상은 남아 있었으나 외래 추적 검사시 상대정맥 폐색 증상도 호전되었음을 확인할 수 있었다

• 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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• 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.

• 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.

• Tuberculosis and Respiratory Diseases
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• 제75권5호
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• pp.210-213
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• 2013

Superior vena cava syndrome (SVCS) is usually caused by extrinsic compression or invasion of the superior vena cava (SVC) by malignant tumors involving mediastinal structures. Although thymomas are well-known causes of SVCS, cases of SVCS caused by malignant thymomas protruding into adjacent vessels draining the SVC with thrombosis have been very rarely reported worldwide. We experienced a 39-year-old female patient with SVCS that developed after the direct invasion of the left brachiocephalic vein (LBCV) and SVC by an anterior mediastinal mass with a high maximum standardized uptake value on the chest computed tomography (CT) and positron emission tomography-CT. Based on these results, she underwent en bloc resection of the tumor, including removal of the involved vessels, and was eventually diagnosed as having a type B2 thymoma permeating into the LBCV and SVC. We present this case as a very rare form of SVCS caused by an invasive thymoma.

• Journal of Chest Surgery
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• 제27권11호
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• pp.953-956
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• 1994

This is a case report of superior vena cava syndrome due to thyroglossal duct cyst, which was surgically treated. The patient was 61 year old male who progressively complained exertional dyspnea for about 5 months and right ptosis, facial flushing, and nasal stuffiness for about 1 month before admission. The CT scan of the thorax revealed the right paratracheal cystic mass that compressed and displaced the trachea to leftward and SVC to rightward. The resection of the cystic mass was performed through the right posterolateral thoracotomy. The pathologic result was compatible with thyroglossal duct cyst. The postoperative status of the patient was uneventful.

• Journal of Chest Surgery
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• 제20권1호
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• pp.218-222
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• 1987

Unroofed coronary sinus syndrome is an uncommon anomaly, Unroofed coronary sinus syndrome is caused by incomplete formation of the left atriovenous fold, and it usually is associated with Left SVC. If it is not diagnosed, a residual reversed or bidirectional shunt will result, and its complications will reduce life expectancy. We experienced 3 cases of unroofed coronary sinus syndrome which combines TOF with PLSVC, partial ECD, primum type ASD. In case of Unroofed coronary sinus syndrome which combines TIF with PLSVC, preoperative diagnosis was not made. In corrective operation for TOF of this case, pump weaning was failed due to hypoxia and cardiac arrest, and he expired at operation room. At autopsy of this case, complete unroofed coronary sinus was found. In the other 2 cases, partial unroofed coronary sinus syndrome was found in operation field and corrective operation was performed successfully. We report these 3 experiences with its review. ^u ++ Noninvasive Assessment of Pressure Gradients across Prosthetic Heart Valve by Doppler Ultrasound - A comparative study of the Duromedics Bileaflet Valves in mitral position and Normal Mitral Valves -with its review.