Levoatriocardinal Vein Combined with Pulmonary Venous Varix Mimicking Arteriovenous Malformations: A Case Report

전주희,강은주,조정현,이기남 대한영상의학회 2021 대한영상의학회지 Vol.82 No.2

The levoatriocardinal vein is an uncommon pulmonary venous abnormality that connects the left atrium or pulmonary vein with the systemic vein. It is distinct from partial anomalous pulmonary venous return in that the former forms a connection with the left atrium through the normal pulmonary vein whereas the latter involves pulmonary venous drainage to the systemic vein. Herein, we describe a case of the levoatriocardinal vein initially misdiagnosed as a pulmonary arteriovenous malformation using chest radiography and chest CT. The levoatriocardinal vein combined with pulmonary venous varix was confirmed using pulmonary angiography. To the best of our knowledge, this unusual coexistence of the levoatriocardinal vein and pulmonary venous varix has not been reported in English literature.

Individual Pulmonary Vein Atresia in Adults: Report of Two Cases

이형남,김영통,조성식 대한영상의학회 2011 Korean Journal of Radiology Vol.12 No.3

We present two cases of individual pulmonary vein atresia without vestige of an involved pulmonary vein. On CT, we noted the absence or interruption of normal pulmonary venous structures, and the presence of abnormal vascular structures that represented collaterals for the involved lung parenchyma. On angiography, the atretic pulmonary vein was found to drain into the other ipsilateral pulmonary veins through the collaterals.

Angiographic Findings of an Isolated Meandering Pulmonary Vein: A Case Report

고지수,권려민,김한면,우지영,김유나,문정원 대한영상의학회 2021 대한영상의학회지 Vol.82 No.4

A meandering pulmonary vein (MPV) is a rare pulmonary vascular anomaly characterized by an abnormal course of the pulmonary vein draining into the left atrium. We report the case of a 55-year-old female who was diagnosed with a right MPV on pulmonary angiography. Enhanced chest CT revealed a vascular structure with an abnormal course that drained into the right superior pulmonary vein in the right upper lobe, which resembled a pulmonary arteriovenous malformation (AVM). Pulmonary angiography performed to discriminate between an MPV and pulmonary AVM showed no feeding artery, normal parenchymal staining, and drainage to the left atrium via the culprit vessel. Thus, the patient was diagnosed with MPV. When an MPV is difficult to differentiate from other vascular anomalies on enhanced chest CT, pulmonary angiography can be helpful. By recognizing the angiographic findings of an MPV, unnecessary treatment can be prevented.

Hemodynamic Change in Pulmonary Vein Stenosis after Radiofrequency Ablation: Assessment with Magnetic Resonance Angiography

Yun, Doyoung,Jung, Jung Im,Oh, Yong Seog,Youn, Ho-Joong The Korean Society of Radiology 2012 KOREAN JOURNAL OF RADIOLOGY Vol.13 No.6

<P>We present a case of pulmonary vein (PV) stenosis after radio-frequency (RF) ablation, in which a hemodynamic change in the pulmonary artery was similar to that of congenital PV atresia on time-resolved contrast-enhanced magnetic resonance angiography (TR-MRA). A 48-year-old man underwent RF ablation due to atrial fibrillation. The patient subsequently complained of hemoptysis, dyspnea on exertion, and right chest pain. Right PV stenosis after catheter ablation was diagnosed through chest computed tomography and lung perfusion scan. Pulmonary TR-MRA revealed the pulmonary artery via systemic arterial collaterals and draining systemic collateral veins. On a velocity-encoded cine image, the flow direction of the right pulmonary artery was reversed in the diastolic phase and the left pulmonary artery demonstrated continuous forward flow throughout the cardiac cycle. These hemodynamic changes were similar to those seen in congenital unilateral PV atresia.</P>

Hemodynamic Change in Pulmonary Vein Stenosis after Radiofrequency Ablation: Assessment with Magnetic Resonance Angiography

윤도영,정정임,오용석,윤호중 대한영상의학회 2012 Korean Journal of Radiology Vol.13 No.6

We present a case of pulmonary vein (PV) stenosis after radio-frequency (RF) ablation, in which a hemodynamic change in the pulmonary artery was similar to that of congenital PV atresia on time-resolved contrast-enhanced magnetic resonance angiography (TR-MRA). A 48-year-old man underwent RF ablation due to atrial fibrillation. The patient subsequently complained of hemoptysis, dyspnea on exertion, and right chest pain. Right PV stenosis after catheter ablation was diagnosed through chest computed tomography and lung perfusion scan. Pulmonary TR-MRA revealed the pulmonary artery via systemic arterial collaterals and draining systemic collateral veins. On a velocity-encoded cine image, the flow direction of the right pulmonary artery was reversed in the diastolic phase and the left pulmonary artery demonstrated continuous forward flow throughout the cardiac cycle. These hemodynamic changes were similar to those seen in congenital unilateral PV atresia.

총폐정맥환류이상증의 외과적 치험 4례

한동기 대한흉부심장혈관외과학회 1994 Journal of Chest Surgery (J Chest Surg) Vol.27 No.1

This is case report of total anomalous pulmonary venous return with atrial septal defect which were corrected surgically by intracardiac procedure under total cardiopulmonary bypass.Two patients were supracardiac type,cardiac and mixed type was each one.The mixed type was three years old female patient.She was diagnosed as atrial septal defect with partial anomalous pulmonary venous return[right pulmonary vein drains into superior vena cava and right atrium] and corrected as usual.After operation,she underwent exertional dyspnea and frequent tachycardia.Chest x-ray film showed pulmonary congestion.Follow up cardiac cineangiogram revealed that left pulmonary vein also anomalously drained into left innominate vein through vertical vein.Through left thoracotomy,anastomosis was successfully carried between left atrium and vertical vein without cardiopulmonary bypass and there was no sign of pulmonary artery obstruction for two years follow up.The other three patient were corrected successfully without complication and got good result.

정상적인 해부학적 연결을 가진 선천성 폐정맥 협착증 -치험 1예 보고-

박준석,장윤희,정미진,강이석,전태국 대한흉부외과학회 2004 Journal of Chest Surgery (J Chest Surg) Vol.37 No.4

Congenital pulmonary vein stenosis is a rare anomaly and related to high mortality due to progressive pulmonary hypertension and heart failure in infancy. Aggressive anti-failure medication and surgical treatment is recommended. Surgical options are balloon dilatation, endovascular stent, pneumonectomy, lung transplantation, patch grafting, and sutureless repair. We report a case of congenital pulmonary vein stenosis with normal anatomical connection successfully treated with sutureless technique and using pulmonary vasodilators, such as Sildenafil, Iloprost and iNO postoperatively. 선천성 폐정맥 협착증은 매우 드문 기형으로 진행성 폐동맥 고혈압 및 조기 심부전으로 사망률이 높아 적극적인 내외과적 치료가 요구된다. 수술적 치료법으로는 풍선 확장술, 스텐트 삽입술, 전폐절제술, 폐이식술, 패취 봉합술, 그리고 무봉합 교정술 등이 있다. 본원에서는 정상적인 해부학적 연결을 가진 폐정맥 협착증에서 무봉합 교정술 및 수술 후 Sildenafil, Iloprost 그리고 NO gas 등의 폐혈관 확장제를 사용하여 성공적으로 치료한 1예를 경험하여 이를 보고하고자 한다.

위급한 객혈을 동반한 일측성 폐정맥 협착증 -1예 보고-

이정렬,이재항,강창현,노정일,서정욱 대한흉부외과학회 2005 Journal of Chest Surgery (J Chest Surg) Vol.38 No.10

환아는 생후 18개월 된 여아로 반복적인 위급한 과량의 객혈을 주소로 입원하였다. 과거력상 생후 6개월에 중증의 심비대 소견을 보이는 심방중격결손증을 진단받았으며 폐정맥 협착이 심비대에 의한 압박으로 생긴 이차적인 병변일 것이라 추정하여 심방중격결손폐쇄술만 시행하였다. 술 후 환아는 심비대와 폐정맥 협착이 완화된 소견을 보였다. 그러나 추적 관찰 중 환아는 반복적인 다량의 객혈로 다시 입원하였고 전산화단층촬영 소견 상 폐정맥 협착이 다시 심해진 것으로 판독되었으며 기관지 주변에 성상을 알 수 없는 연조직 종괴들이 좌측 기관지를 압박하고 있었다. 정확한 위치를 알 수 없는 반복적인 객혈로 인해 시험적 개흉술이 불가피하였고, 수술 소견상 좌폐정맥은 하나였으며 외견상 협착의 소견을 보였다. 좌측 기관지 주변에는 다발성 임파절 비대가 기관지를 압박하고 있었다. 또한 수술 중 다량의 객혈이 발생하여 전폐절제술을 시행할 수 밖에 없었다. 술 후 병리 소견은 폐정맥 협착과 일치하였다. 환아는 2일간의 중환자실 관리 후 6일째 합병증 없이 퇴원하였다. 2개월간 추적 관찰되었으며 증상 없이 양호한 경과를 보이고 있다. 그러나 향후 지속적인 추적 관찰이 필요할 것으로 생각한다. A case is described in a girl who presented with recurrent life-threatening hemoptysis at the age of 18 months, and had been diagnosed as atrial septal defect with severe cardiomegaly which was presumed to result in pulmonary vein stenosis at the age of 6 months. Closure of atrial septal defect was associated with decreased heart size and improved pulmonary venous flow. However, recurrent life-threatening hemoptysis occurred during follow-up. Computed tomography scan demonstrated left pulmonary vein stenosis and extrinsic compression of the left bronchus by multiple soft tissue density-masses. Exploratory thoracotomy revealed single stenotic left pulmonary vein, and flat left main bronchus compressed by multiple hypertrophied lymph nodes. Unexpected endotrachial tube bleeding during left hilar dissection mandated to proceed to left pneumonectomy. The patient's postoperative course was uneventful. Follow-up chest roentgenography revealed acceptable left hydrothorax without mediastinal shifting. Nevertheless, a long-term follow-up is necessary.

폐정맥의 원발성 악성 말초신경초종: 증례 보고

Hyun Woo,Hyeyoung Kwon,Jin Hwan Kim,Song Soo Kim,Hyung Kyu Park,Younju Rhee,Jae-Hyeong Park 대한영상의학회 2023 대한영상의학회지 Vol.84 No.6

Primary masses rarely originate from the heart and great vessels, and a malignant peripheral nerve sheath tumor (MPNST) is extremely rare. A 76-year-old male with pleural effusion underwent contrast- enhanced computed tomography, which revealed a hypoattenuating mass involving the right pulmonary vein and left atrium. Ultrasonography showed that the mass originated from the right pulmonary vein. Surgical resection confirmed an MPNST that originated from the pulmonary vein. We report the first Korean case of a primary MPNST originating from the pulmonary vein. We have also described the radiologic findings suggestive of a pulmonary vein mass.

Pulmonary Embolism Caused by Popliteal Venous Aneurysm

홍대진,송석원 대한흉부외과학회 2013 Journal of Chest Surgery (J Chest Surg) Vol.46 No.1

Venous aneurysms are uncommon in the lower limb and are more frequently found in the neck and thoracic and visceral veins. However, they have been reported to cause thrombosis, pulmonary thromboembolism, and other related complications. Popliteal venous aneurysms are often undetected because they are usually asymptomatic, but they may cause pulmonary thromboembolic events. We experienced a case of a 44-year-old man who was referred for recurrent pulmonary thromboembolism. He showed no other symptoms or signs except shortness of breath. A popliteal venous aneurysm was diagnosed incidentally because the examinations were performed to detect a deep vein thrombosis in relationship to the patient’s history of pulmonary thromboembolism. We report a case of surgical treatment for a popliteal venous aneurysm that was complicated by pulmonary thromboembolism.