The Experts below are selected from a list of 6 Experts worldwide ranked by ideXlab platform
Kye Chul Shin - One of the best experts on this subject based on the ideXlab platform.
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A Case of the Bronchial Artery-Pulmonary Vein Malformation
Tuberculosis and Respiratory Diseases, 1995Co-Authors: Young Il Jo, Kwang Seon Song, Suk Joong Yong, Kye Chul ShinAbstract:The bronchial artery-Pulmonary Vein Malformation should be called the systemic artery-to-Pulmonary Vein arterioveonus Malformation in the lung. Although Pulmonary arteriovenous Malformation has been well documented in intraPulmonary arteriovenous Malformation, the systemic artery-to-Pulmonary Vein arteriovenous Malformation is rare. Most patients with systemic artery-to-Pulmonary Vein arteriovenous Malformation is asymptomatic and the diagnosis of these anomaly may be done by continuous murmur or abnormal chest X-ray on the physical examination. The pathogenesis of this condition is congenital Malformation which explains these anastomoses between the Pulmonary Vein and accessory brachial arteries and acquired Malformation which explains development of new blood vessel to supply large enough to cause significant systemic-Pulmonary shunts due to inflammation secondary to infection, trauma, or previous surgery. We experienced a case of the bronchial artery-Pulmonary Vein Malformation which was detected on angiography in 20-year-old women whose chief complain is hemoptysis. This massive hemoptysis was controlled by selective brachial artery embolization with Gelfoam and Ivalon particles.
Young Il Jo - One of the best experts on this subject based on the ideXlab platform.
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A Case of the Bronchial Artery-Pulmonary Vein Malformation
Tuberculosis and Respiratory Diseases, 1995Co-Authors: Young Il Jo, Kwang Seon Song, Suk Joong Yong, Kye Chul ShinAbstract:The bronchial artery-Pulmonary Vein Malformation should be called the systemic artery-to-Pulmonary Vein arterioveonus Malformation in the lung. Although Pulmonary arteriovenous Malformation has been well documented in intraPulmonary arteriovenous Malformation, the systemic artery-to-Pulmonary Vein arteriovenous Malformation is rare. Most patients with systemic artery-to-Pulmonary Vein arteriovenous Malformation is asymptomatic and the diagnosis of these anomaly may be done by continuous murmur or abnormal chest X-ray on the physical examination. The pathogenesis of this condition is congenital Malformation which explains these anastomoses between the Pulmonary Vein and accessory brachial arteries and acquired Malformation which explains development of new blood vessel to supply large enough to cause significant systemic-Pulmonary shunts due to inflammation secondary to infection, trauma, or previous surgery. We experienced a case of the bronchial artery-Pulmonary Vein Malformation which was detected on angiography in 20-year-old women whose chief complain is hemoptysis. This massive hemoptysis was controlled by selective brachial artery embolization with Gelfoam and Ivalon particles.
Kwang Seon Song - One of the best experts on this subject based on the ideXlab platform.
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A Case of the Bronchial Artery-Pulmonary Vein Malformation
Tuberculosis and Respiratory Diseases, 1995Co-Authors: Young Il Jo, Kwang Seon Song, Suk Joong Yong, Kye Chul ShinAbstract:The bronchial artery-Pulmonary Vein Malformation should be called the systemic artery-to-Pulmonary Vein arterioveonus Malformation in the lung. Although Pulmonary arteriovenous Malformation has been well documented in intraPulmonary arteriovenous Malformation, the systemic artery-to-Pulmonary Vein arteriovenous Malformation is rare. Most patients with systemic artery-to-Pulmonary Vein arteriovenous Malformation is asymptomatic and the diagnosis of these anomaly may be done by continuous murmur or abnormal chest X-ray on the physical examination. The pathogenesis of this condition is congenital Malformation which explains these anastomoses between the Pulmonary Vein and accessory brachial arteries and acquired Malformation which explains development of new blood vessel to supply large enough to cause significant systemic-Pulmonary shunts due to inflammation secondary to infection, trauma, or previous surgery. We experienced a case of the bronchial artery-Pulmonary Vein Malformation which was detected on angiography in 20-year-old women whose chief complain is hemoptysis. This massive hemoptysis was controlled by selective brachial artery embolization with Gelfoam and Ivalon particles.
Suk Joong Yong - One of the best experts on this subject based on the ideXlab platform.
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A Case of the Bronchial Artery-Pulmonary Vein Malformation
Tuberculosis and Respiratory Diseases, 1995Co-Authors: Young Il Jo, Kwang Seon Song, Suk Joong Yong, Kye Chul ShinAbstract:The bronchial artery-Pulmonary Vein Malformation should be called the systemic artery-to-Pulmonary Vein arterioveonus Malformation in the lung. Although Pulmonary arteriovenous Malformation has been well documented in intraPulmonary arteriovenous Malformation, the systemic artery-to-Pulmonary Vein arteriovenous Malformation is rare. Most patients with systemic artery-to-Pulmonary Vein arteriovenous Malformation is asymptomatic and the diagnosis of these anomaly may be done by continuous murmur or abnormal chest X-ray on the physical examination. The pathogenesis of this condition is congenital Malformation which explains these anastomoses between the Pulmonary Vein and accessory brachial arteries and acquired Malformation which explains development of new blood vessel to supply large enough to cause significant systemic-Pulmonary shunts due to inflammation secondary to infection, trauma, or previous surgery. We experienced a case of the bronchial artery-Pulmonary Vein Malformation which was detected on angiography in 20-year-old women whose chief complain is hemoptysis. This massive hemoptysis was controlled by selective brachial artery embolization with Gelfoam and Ivalon particles.
Hae Ryong Song - One of the best experts on this subject based on the ideXlab platform.
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Pulmonary manifestations in Proteus syndrome: Pulmonary varicosities and bullous lung disease.
American Journal of Medical Genetics Part A, 2011Co-Authors: Kyung Hee Kang, Hae Ryong SongAbstract:: We report on two patients with Proteus syndrome (PS), with emphasis on its Pulmonary manifestations. The first patient was a 6-year-old girl diagnosed with PS at 5 years of age. The Pulmonary abnormalities first observed at age 3 years and included streaky densities with accentuated vascular markings detected by chest radiography. The patient had persistent abnormalities on follow-up chest radiographs. Chest computed tomography (CT) scans showed diffuse Pulmonary venous dilatations. The second patient was a 10-year-old boy diagnosed with PS at age 4 years. Chest radiography and CT scans showed patchy and streaky densities intermixed with small bullae, which were interpreted as pneumonia with post-inflammatory pneumatoceles. The patient developed diffuse enlargement of air spaces of the lungs at age 10 years with severe respiratory compromise. Although Pulmonary manifestations in PS are uncommon, recognition of Pulmonary Vein Malformation and the presentation of enlarged air spaces in the lungs at an earlier age are important for accurate diagnosis. The plain radiograph findings of accentuated vascular markings seen in patients with PS may appear similar to interstitial or chronic pneumonia. This report emphasizes the features of lung involvement in children with PS and suggests that specific attention be paid to Pulmonary manifestations using chest CT scans. © 2011 Wiley-Liss, Inc.
