• 제목/요약/키워드: Pulmonary Artery

검색결과 838건 처리시간 0.022초

Traumatic Right Pulmonary Artery Rupture after Accidentally Being Stepped on the Chest

  • Son, Shin-Ah;Bae, Chae-Min;Oh, Tak-Hyuk;Do, Young Woo;Seok, Yangki;Cho, Joon Yong
    • Journal of Chest Surgery
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    • 제52권5호
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    • pp.380-383
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    • 2019
  • Traumatic pulmonary artery rupture is a rare, life-threatening injury. Currently, no strict guidelines for its management exist. Herein, we report a successful surgical repair of a right pulmonary artery rupture caused by being stepped on.

Calcified Dirofilaria immitis Mimicking Thoracic Foreign Body in a Dog

  • Yeongseok Jeong;Seungjo Park
    • 한국임상수의학회지
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    • 제40권6호
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    • pp.457-463
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    • 2023
  • A 13-year-old neutered male Pomeranian, weighting 3 kg, presented with respiratory distress and depression. Radiographic examination revealed calcified ring-like opacities in the main pulmonary artery, mimicking thoracic foreign bodies. Additionally, right heart and main pulmonary artery enlargement and notable lung infiltrations were also observed. Echocardiography showed coil shaped structures in the main pulmonary artery with increased echogenicity compared to other nearby heartworms, which is consistent with calcified Dirofilaria immitis (heartworms). The dog was diagnosed with caval syndrome, which is the advanced and severe manifestation of heartworm infection. This report presents a rare case of calcified heartworm infection observed during a radiological examination, which resemble foreign bodies. Therefore, chronic heartworm disease should be considered as a differential diagnosis when radiopaque ring-like opacities are observed in the pulmonary artery on thoracic radiographs.

우하횡경막동맥-폐동맥 문합부위의 가성동맥류로 인한 객혈로 색전술 후 성공한 예 (Successful Embolization in the Patient with Hemoptysis Due to Right Inferior Phrenic Artery-pulmonary Artery Anastomosis and Pseudoaneurysm)

  • 박현웅;이고은;박용성;손지웅;최유진;나문준;권선중
    • Tuberculosis and Respiratory Diseases
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    • 제66권4호
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    • pp.319-323
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    • 2009
  • 객혈의 원인혈관은 대부분 기관지동맥이다. 하지만 다른 전신혈관 및 폐동맥에 의한 객혈도 항상 염두에 둬야하고, 만약 기관지동맥색전술 후 객혈이 지속되거나 기관지동맥에서 출혈의 원인을 찾지 못하면 다른 전신혈관에 대한 검사를 시행하여야 한다. 전신혈관-폐혈관의 문합이나 폐동맥 가성동맥류는 매우 드문 폐혈관질환으로 여러원인에 의해서 발생할 수 있으며, 이로 인한 객혈이 발생할 경우 생명을 위협할 수 있기 때문에 정확하고 빠른 진단과 치료가 필요하다. 저자는 77세 남자로 우하횡경막동맥-폐동맥 문합 및 문합부위 가성동맥류로 인한 지속적인 객혈로 내원하여, 색전술로 성공적으로 치료된 환자를 경험하여 이를 보고한다.

Fontan 수술후 저심장박출증 및 지속성 흉막 삼출액이 발생되는 해부생리학적 원인 (Modified Fontan Operation: Physio-anatomic Causes of Low Cardiac Output and Persistent Pleural Effusion)

  • 한재진;서경필
    • Journal of Chest Surgery
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    • 제23권2호
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    • pp.213-221
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    • 1990
  • We have experienced 62 cases of modified Fontan operations in Seoul Nat’l University Hospital from Apr. 1986 to Jul. 1989, They were 38 males and 24 females, and their age was ranged from 16 months to 15.5 years of age. [mean age : 5.73$\pm$2.99 years] There were 16 operative deaths and 2 late deaths, therefore 29% of overall mortality. Their diagnoses were as follows; 28 single ventricle, 11 tricuspid atresia, 6 DORV with LV hypoplasia, 3 pulmonary atresia with hypoplastic RV, 3 TGA with hypoplastic RV, 3 cor\ulcornerGA with hypoplastic LV and PA, 6 AV canal defects with PA, and 2 others. Low cardiac output and pleural effusion were developed frequently, so we divide 40 patients into some groups to analyze the physiologic and anatomic causes of them. By the degree of the LCO, group A was no LCO[mean amount of inotropics used: 0-5 \ulcornerg/kg/min] with 17 cases, B mild LCO [5-10] with 11, C moderate to severe LCO but alive[>10] with 8, D severe LCO to death with 4 cases. For the pleural effusion, group 1 was to be removed the chest tube within 1 week with 8 cases, group II within 3 weeks with 21 cases, group III beyond 3 weeks with 12 cases. We considered their age, diagnosis, pulmonary artery size[PA index], pulmonary artery abnormality, palliative shunt, systemic ventricular type, pulmonary artery wedge pressure, as preoperative factors, and operative methods, and as postoperative factors, CVP, LAP, arrhythmia, thrombosis, atrioventricular valvular insufficiency, etc. In the view of LCO, pulmonary artery size and PCWP were statistically significant [P<0.05], and arrhythmia, A-V valve insufficiency were inclined to the group C and D Pleural effusion was influenced by the pulmonary artery size, pulmonary artery resistance, PCWP, and CVP significantly. [P<0.05] And arrhythmia, residual shunt, and A-V valvular insufficiency were inclined to group II and III, too. As a results, the followings are to be reminded as the important factors at the care of post-Fontan LCO, and persistent pleural effusion [1] pulmonary artery size, [2] pulmonary artery resistance, [3] PCWP, [4] CVP, [5] arrhythmia, [6] residual shunt, [7]A-V valvular insufficiency.

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Embolization of Multiple Systemic Artery to Pulmonary Artery Fistula with Recurrent Hemoptysis

  • Lee, Jung-Kyu;Park, Ju-Hee;Kim, Junghyun;Kim, Soo Jung;Lee, Ae-Ra;Lee, Chang Hoon;So, Young-Ho
    • Tuberculosis and Respiratory Diseases
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    • 제75권3호
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    • pp.120-124
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    • 2013
  • Herein, we report a case of multiple systemic arteries to pulmonary artery fistulas without any underlying causes, presenting recurrent hemoptysis. Transcatheter embolization was successfully performed several times on multiple systemic feeding arteries. Multiple systemic arteries to pulmonary fistulas can be a source of uncontrolled bleeding, and embolization may be a reasonable therapeutic option to control the bleeding.

고립성 우측 폐동맥 형성부전증 1례 (A Case of Isolated Right Pulmonary Artery Agenesis)

  • 김도연;이재성;김영;장윤수;김형중;김태훈;안철민
    • Tuberculosis and Respiratory Diseases
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    • 제57권5호
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    • pp.489-493
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    • 2004
  • 일측성 폐동맥 형성부전증은 매우 드문 선천성 기형으로서 대부분 팔로사징, 심실중격결손등과 같은 선천성 심기형을 동반하며 선천성 심기형이 동반되지 않은 고립성 편측 폐동맥 형성부전증은 극히 드물다. 이러한 환자들의 경우 성인이 될때까지 무증상으로 지내는 경우가 많으며 흉부 방사선 검사상 병변측 폐의 폐음영은 과투과되어 나타나며 흉곽은 작아진 소견으로부터 고립성 편측 폐동맥 형성부전증을 의심하게 된다. 저자들은 경미한 운동시 호흡곤란을 증상으로 내원한 50세 여환에서 흉부 전산화 단층촬영 및 환기-관류 스캔과 심초음파검사를 시행하고, 삼차원 재구성 전산화 심혈관 단층촬영을 이용하여 고립성 우측 폐동맥 형성부전증을 진단하고 치료한 1례를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

대동맥벽내 혈종 환자에서의 폐동맥 외막주위 혈종: 증례 보고 (Pulmonary Artery Periadventitial Hematoma in a Patient with Aortic Intramural Hematoma: A Case Report)

  • 권훈;정연주;이지원;황민희;김진유;이남경;이지원
    • 대한영상의학회지
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    • 제85권3호
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    • pp.649-653
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    • 2024
  • 폐동맥 외막주위 혈종은 Stanford A형 대동맥벽내 혈종의 드문 합병증이다. 근위부 상행 대동맥과 폐동맥은 공통된 혈관외막을 공유하고 있기 때문에 대동맥벽내 혈종의 혈액은 폐동맥으로 확산될 수 있다. 저자들은 급성 흉통을 호소하는 66세 남성에게서 보인 Stanford A형 대동맥벽내 혈종과 연관된 폐동맥 외막주위 혈종의 증례를 보고하고자 한다.

심장외 도관을 사용치 않고 시행한 우심실 성형술 (Roconstruction of the Pulmonary Outflow Tract withou Proshetic Conduit)

  • 김진국
    • Journal of Chest Surgery
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    • 제21권6호
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    • pp.1124-1136
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    • 1988
  • Massive hemoptysis, usually rapid flooding of tracheobronchial tree and asphyxia, is associated with high mortality. We have controlled massive hemoptysis in two cases with use of bronchial artery angiography & selective bronchial artery embolization with Gelfoam particle. One case was inoperable case that was confirmed as TOF c severe pulmonary artery hypoplasia with massive hemoptysis due to hypertrophied bronchial artery and its collaterals. Another case was congenital ASD with pulmonary Aspergillosis, postop. empyema and BPF associated with massive bleeding due to erosion of hypervascular bronchial artery. We experienced dramatic improvement of general condition and cessation of massive hemoptysis for above two cases. No other problems and complication were noted during postop. hospitalization and follow-up period.

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양축에 발생한 엽내형 폐격리증의 외과적 치료 -1례 보고- (Surgical treatment of bilateral pulmonary sequestraion; -report of A case-)

  • 손재문
    • Journal of Chest Surgery
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    • 제28권8호
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    • pp.792-796
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    • 1995
  • The pulmonary sequestration is a rare congenital malformation of the lung, concerning about the abnormal feeding systemic artery, may happen a serious complication of bleeding during operation if not recognized before operation. We experienced a case of bilateral intralobar pulmonary sequestration preoperatively confirmed by aortogram. An Aortogram demonstrated a anomalous systemic artery arising from thoracic aorta just above the diaphragm. The artery bifurcated and supplied areas of both right and left lower lobes. On the operative field, left lower lobectomy was done with devision and ligation of left branch of anomalous artery and triple ligation of remained branch of anomalous artery was done. Postoperative course was uneventful. She was discharged on postoperative seventeenth day.

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동맥관 개존증을 동반한 주폐동맥의 동맥류 치험 1예 (Aneurysm of the main pulmonary artery associated with patent ductus arteriosus)

  • 염욱;조대윤;노준량
    • Journal of Chest Surgery
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    • 제15권4호
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    • pp.381-386
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    • 1982
  • Pulmonary artery aneurysm usually carries an ominous prognosis due to the associated pulmonary hypertension. In July 1981, a patient with a huge aneurysm of main pulmonary artery secondary to pulmonary hypertension and bacterial endocarditis due to a patent ductus arteriosus was treated by resection of the aneurysm and Dacron patch graft replacement and closure of the patent ductus arteriosus. The immediate postoperative result was excellent. We now report the surgical treatment, clinical course, and one and half years follow up of the patient.

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