• Korean Journal of Radiology
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• 제24권4호
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• pp.349-361
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• 2023

Objective: To quantitatively assess the pulmonary vasculature using non-contrast computed tomography (CT) in patients with chronic thromboembolic pulmonary hypertension (CTEPH) pre- and post-treatment and correlate CT-based parameters with right heart catheterization (RHC) hemodynamic and clinical parameters. Materials and Methods: A total of 30 patients with CTEPH (mean age, 57.9 years; 53% female) who received multimodal treatment, including riociguat for ≥ 16 weeks with or without balloon pulmonary angioplasty and underwent both non-contrast CT for pulmonary vasculature analysis and RHC pre- and post-treatment were included. The radiographic analysis included subpleural perfusion parameters, including blood volume in small vessels with a cross-sectional area ≤ 5 mm² (BV5) and total blood vessel volume (TBV) in the lungs. The RHC parameters included mean pulmonary artery pressure (mPAP), pulmonary vascular resistance (PVR), and cardiac index (CI). Clinical parameters included the World Health Organization (WHO) functional class and 6-minute walking distance (6MWD). Results: The number, area, and density of the subpleural small vessels increased after treatment by 35.7% (P < 0.001), 13.3% (P = 0.028), and 39.3% (P < 0.001), respectively. The blood volume shifted from larger to smaller vessels, as indicated by an 11.3% increase in the BV5/TBV ratio (P = 0.042). The BV5/TBV ratio was negatively correlated with PVR (r = -0.26; P = 0.035) and positively correlated with CI (r = 0.33; P = 0.009). The percent change across treatment in the BV5/TBV ratio correlated with the percent change in mPAP (r = -0.56; P = 0.001), PVR (r = -0.64; P < 0.001), and CI (r = 0.28; P = 0.049). Furthermore, the BV5/TBV ratio was inversely associated with the WHO functional classes I-IV (P = 0.004) and positively associated with 6MWD (P = 0.013). Conclusion: Non-contrast CT measures could quantitatively assess changes in the pulmonary vasculature in response to treatment and were correlated with hemodynamic and clinical parameters.

• Tuberculosis and Respiratory Diseases
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• 제62권5호
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• pp.359-364
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• 2007

• Tuberculosis and Respiratory Diseases
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• 제42권6호
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• pp.913-922
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• 1995

연구배경: 혈류의 누가현상이 일어나는 폐혈관계의 압력을 유효유출압($P_I$), 심박출량의 변화분에 대한 폐동맥압의 변화분을 폐혈관저항증분(IR)이라고 정의할때에 $P_I$ 및 IR과 폐혈관저항을 비교해보면 폐혈관저항의 문제점이 발견된다. 즉 폐혈관상이 감소하는 폐색전증에서는 이론상 IR이 주로 증가해야 하는데, 여러 연구에 의하여 상반된 결과가 보고되어있고 폐혈관저항과 $P_I$, IR간에는 상위점이 존재하는 것이 알려져 왔다. 이에 따라 본 연구에서는 폐혈관저항을 폐혈관계의 유효유출압($P_I$)과 폐혈관저항증분(IR)으로 세분할때 폐색전증의 유발 및 치료시 아들이 어떻게 변화하는가를 관찰하여 이러한 새로운 지표들의 의미와 일반적으로 사용되는 폐혈관저항과의 차이점을 알아보고자 하였다. 방법: 실험전에 동정맥루를 만든후 10~15분 간격으로 조직하여, 동정맥루가 모두 폐쇄된 상태, 하나의 동정맥루가 개방된 상태, 그리고 두개의 동정맥루가 모두 개방된 상태의 3가지 경우로 심박출량올 변화시키면서 방사성동위원소로 표지된 자가혈병으로 대량의 폐색전증을 유발시킨후의 평균폐동맥압을 측정하여 폐혈관계의 유효유출압과 폐혈관저항증분을 계산하였다. 이때 대조군은 특이 치료를 하지않고, 제 1 치료군은 15분 동안, 제 2치료군은 3시간에 걸쳐서 재조합형의 조직형 플라스미노겐 활성체를 체중당 1mg씩 정맥주입하면서 유효유출압과 폐혈관저항증분의 변화양상을 관찰하였다. 곁과: 1) 폐혈관저항은 폐동맥압의 변화양상과 유사하게 변화했는데, 세군 모두 폐혈관저항이 유의하게 증가하였고, 제 1 치료군 및 제 2 치료군에서는 치료후 폐혈관저항이 계속 감소하는 경향을 보였는데, 제 1 치료군의 감소속도가 제 2 치료군보다 유의하게 빨랐다. 2) 최소자승법으로 산출한 심박출량과 폐동맥압과의 직선관계는 절편($P_I$) 및 기울기(IR)가 유의하였다. 3) $P_I$(폐혈관계의 유효유출압)는 폐혈관저항과 동일한 양상으로 변화한 반면에, 이론상 폐혈관저항과 가까운 IR(폐혈관저항증분)에서는 세군간의 유의한 차이나 조직형 플라스미노겐 활성체 투여후의 의미있는 변화는 거의 없었다. 결론: 폐색전증에서는 폐혈관계의 실제저항을 의미하는 폐혈관저항증분과 폐색전증에 대한 이차적 혈관 수축때문에 생기는 폐혈관계의 유효유출압의 변화가 동시에 반영된다고 할 수 있겠다.

• Journal of Chest Surgery
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• 제18권2호
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• pp.327-333
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• 1985

Pulmonary arteriovenous fistula is a congenital malformation of the pulmonary vasculature in which there is a persistence of one or more sizable communications that bypass the pulmonary capillary bed that thus directs unoxygenated pulmonary arterial blood directly into the pulmonary venous system. The developmental cause of pulmonary arteriovenous fistula is unknown, but it is postulated that the abnormal channels represent persistent vessels of the primitive splanchnic capillary bed that do not resorb during growth and maturation. We have experienced a case of pulmonary arteriovenous fistula. The 45 years old woman admitted to Kosin Medical College Hospital via emergency room because of massive hemoptysis, and was diagnosed pulmonary arteriovenous fistula by twice postoperative histopathologic examination. The postoperative course was uneventful and she was discharged on the 16th, second postoperative day in a healthy condition.

• Advances in pediatric surgery
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• 제2권2호
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• pp.138-142
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• 1996

Pulmonary sequestration is a complex anomaly involving the pulmonary parenchymal tissue and its vasculature. It presents as a cystic mass of nonfunctional lung tissue without communication with the tracheobronchial system. Usually, it receives blood supply from anomalous systemic vessels. Therefore, preoperative diagnosis of the pulmonary sequestration is difficult, especially when it is located in the abdomen and combined with congenital cystic adenomatoid malformation(CCAM). We encountered such a mass(CCAM type 2) detected prenatally by ultrasonography. It was a kidney bean shaped, pinkish mass straddling the thorax and abdomen on the right side. Because of the sonographic appearance, neuroblastoma was diagnosed preoperatively. The mass was completely extirpated without difficulty.

• 대한핵의학회:학술대회논문집
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• 대한핵의학회 1989년도 제28차 춘계학술대회
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• pp.126.1-126.1
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• 1989

• Journal of Chest Surgery
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• 제25권1호
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• pp.23-31
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• 1992

The ideal approach in the staged management of patients with pulmonary atresia has been a challenging problem and the result has not been always satisfactory. We reviewed our early result of initial palliative surgeries in fifteen cases of pulmonary atresia with interventricular communication Included are eight cases of simple pulmonary atresia with ventricular septal defect and seven cases of pulmonary atresia associated with other complex cardiac anomalies. The ages of the patients were less than one year except one. The morphology of pulmonary vasculature was highly variable and showed unfavorable conditions in most cases. Pulmonary artery was nonconfluent in two. Two-thirds of all cases showed significant problems such as juxtaductal stenosis or diffuse hypoplasia. The ductus arteriosus usually narrowed at its pulmonic end. Initial palliation was done by modified Blalock-Taussig shunt in six, central shunt with or without pulmonary angioplasty in five, right ventricular outflow tract [RVOT] reconstruction in three and direct connection of nonconfluent pulmonary arteries with bilateral cav-opulmonary shunt in one patient. There were 3 hospital deaths. Two of them underwent simultaneous repair of the associated anomaly of TAPVR. Among the six patients who received modified Blalock-Taussig shunt, three needed early second palliative procedure by central shunt, RVOT patch reconstruction and pulmonary angioplasty in each case, All patients who received central shunt showed marked clinical improvement. Among the twelve patients who survived the palliative procedures, two patients underwent total correction 13 months and 18 months after initial palliation respectively. We think that the choice of palliative procedure must be individualized according to the morphology of the pulmonary arteries. More experience and long term follow-up data are necessary to meet this challenging problem.

• Journal of Chest Surgery
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• 제6권2호
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• pp.159-164
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• 1973

Bronchopulmonary sequestration is a congenital malformation characterized by a cystic portion of the lung that derives its arterial blood supply through anomalous aberrant vessel directly of the systemic circulation. An aberrant systemic vessel supplying the lung was reported by Huber in 1777. Although this lesion is uncommon disorder, there are several reports on operative death caused by exanguinating hemorrhage from the aberrant arteries to the bronchopulmonary sequestration to that it has received a great deal of attention. Two type of bronchopulmonary sequestration have been identified: Intralobar pulmonary sequestration is usually contained within the visceral pleura of a pulmonary lobe and its venous drainage to the pulmonary venous system. Extrapulmonary sequestration is usually within the pleural sheath its own and its vasculature drains into the azygos or hemiazygos system. we presented one case of intralobar pulmonary sequestration which led to motor paralysis, chylothorax and hemorrhage that are consequent on postoperative complication.

• 한국임상수의학회지
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• 제19권1호
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• pp.110-113
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• 2002

An atrial septal defect (ASD) is a congenital hole in the atrial septum that allows flow between the two atria. Small ASDs are usually well-tolerated defects and do not result in significant clinical abnormalities. In large ASDs or in the presence of other cardiac defects, clinically significancy is increased. Atrial septal defects in 2 Dogs with cardiac and respiratory signs were diagnosed at seoul animal medical center. In ascultation, systolic murmur and the splitting of second heart sound were heard at pulmonary or tricuspid valve region. In radiograph, right-sided cardiomegaly, pulmonary artery dilation, increased pulmonary vasculature makings, and pleural effusion or pulmonary edema signs were observed. In echocardiography, the region, location and size of septal defect was identified. Also, the direction and degree of shunt was measured. These dogs were treated with medicine for cardiac failure. One dog is well-tolerated, the other dog died.

• Journal of Chest Surgery
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• 제53권5호
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• pp.310-312
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• 2020

Transcatheter leadless pacemaker dislodgment is a rare and potentially fatal complication of leadless device implantation. We present the first case of multidetector computed tomography images of leadless pacemaker migration and embolization in the pulmonary middle lobe artery. The patient was managed by percutaneous retrieval of the dislodged device and re-implantation in the appropriate position.