2.Incidentally Found, Growing Congenital Aneurysm of the Left Atrium.
Jong Seon PARK ; Dong Hyup LEE ; Seung Se HAN ; Mi Jin KIM ; Dong Gu SHIN ; Young Jo KIM ; Bong Sup SHIM
Journal of Korean Medical Science 2003;18(2):262-266
A left atrial aneurysm is a very rare cardiac anomaly that usually develops in the left atrial appendage. It usually develops congenitally, and has a risk of life-threatening complications. Here, we report a case of a growing aneurysm of the left atrium that was incidentally found in a 42-yr-old woman. Eighteen years prior, an abnormal cardiomegaly was found on a chest radiography for a pre-operative study. The chest radiography at this time demonstrated a more prominent cardiomegaly than the previous radiography findings. The left atrial aneurysm was diagnosed by echocardiography and cardiac catheterization. Although asymptomatic, she underwent a successful surgical excision to allay the possibilities of rupture, arrhythmia, heart failure, or thromboembolism. The surgical findings demonstrated an 8 x 15 cm sized saccular aneurysm at the left atrial appendage, and the pathologic findings showed three myocardial layers. The patient has been asymptomatic during the 15 months of follow-up. In conclusion, a congenital left atrial aneurysm can grow with time, even in asymptomatic cases, and an aneurysmectomy is a curative treatment, which can eliminate the potential complications.
Adult
;
Echocardiography
;
Female
;
Heart Aneurysm/congenital*
;
Heart Aneurysm/pathology*
;
Heart Aneurysm/surgery
;
Heart Aneurysm/ultrasonography
;
Heart Atria/pathology*
;
Heart Atria/surgery
;
Heart Atria/ultrasonography
;
Human
3.Surgical Repair of Giant Right Atrial Aneurysm in a Neonate.
Youngok LEE ; Joonyong CHO ; Gunjik KIM ; Sangbum LEE ; Myungchul HYUN ; Yeohyang KIM
Korean Circulation Journal 2011;41(6):331-333
Right atrial aneurysm is an extremity rare congenital heart defect. We report a case which was diagnosed during the early fetal stage and operated on in a 2 week old neonate. Following median sternotomy, aneurysmectomy was performed under a cardiopulmonary bypass. Histopathological examination of the resected atiral tissue showed a lipotomatous degeneration and reduction of the muscular elements. There were no postoperative complications.
Aneurysm
;
Cardiopulmonary Bypass
;
Extremities
;
Heart Aneurysm
;
Heart Atria
;
Heart Defects, Congenital
;
Humans
;
Infant, Newborn
;
Postoperative Complications
;
Sternotomy
4.Clinical Analysis of Open Heart Surgery: A report of 111 cases.
Cheol Joo LEE ; Tae Eun JUNG ; Dong Hyup LEE ; Myeun Shik KANG
Yeungnam University Journal of Medicine 1986;3(1):215-219
During 1986, 111 cases of open heart surgery were performed at Yeungnam University Hospital consisting 88 cases of congenital heart disease and 23 cases of acquired heart disease. Among 88 congenital heart disease, 72 were acyanotic group and 16 were cyanotic. Common congenital heart diseases were ventricular septal defect (51%), atrial septal defect (18%) and Tetralogy of Fallot (16%). Among 23 acquired heart disease, 22 cases were valvular heart disease and one was dissecting aortic aneurysm. Three cases of the postoperative death were present resulting 2.7% of surgical mortality rate.
Aortic Aneurysm
;
Heart Defects, Congenital
;
Heart Diseases
;
Heart Septal Defects, Atrial
;
Heart Septal Defects, Ventricular
;
Heart Valve Diseases
;
Heart*
;
Mortality
;
Tetralogy of Fallot
;
Thoracic Surgery*
5.A Case of Congenital Left Ventricular Aneurysm in an Elderly Woman.
Seong Mi PARK ; Wan Joo SHIM ; Seung Soon RHA ; Sang Won PARK ; Do Sun LIM ; Young Hoon KIM ; Young Moo RO
Journal of the Korean Society of Echocardiography 2002;10(1):79-83
Congenital left ventricular aneurysm is a rare, poorly understood and potentially lethal congenital heart disease. Few pediatric cases have been reported. This aneurysm is defined as a fibrous outpouch with paradoxical contractility and appears to be a developmental anomaly, an idiopathic dysplasia of left ventricular endocardium and myocardium. We report a case of congenital left ventricular aneurysm presenting an abnormal electrocardiography in a 65-year old woman without cardiac symptoms. Congenital left ventricular aneurysm was diagnosed by echocardiography and left ventriculogram.
Aged*
;
Aneurysm*
;
Echocardiography
;
Electrocardiography
;
Endocardium
;
Female
;
Heart Defects, Congenital
;
Humans
;
Myocardium
7.Aneurysm or Diverticulum of Left Ventricle.
Sang Hong BAEK ; Wook Sung CHUNG ; Seung Suk CHUN ; Chong Sang KIM ; Kyu Bo CHOI ; Soon Jo HONG
Korean Circulation Journal 1989;19(4):756-764
Two cases of abnormalities of the left ventricular wall(left ventricular aneurysm or diverticulum) are presented. A saccular deformity of the left ventricle may be and aneurysm or a diverticulum. In one case, the defect seems to be subcalvular aneurysm(or fibrous diverticulum) or aneurysm of the membranous ventricular septum; this lesion seems to be a natural consequence of spontaneous closure of a defect of the membranous septum. The other case, it seems that the defect is ventricular aneurysm with syndrome of myocardial infarction and normal coronary arteries, or double or accessory chambered left ventricle. The thromboembolic phenomenon was noted on a left frontoparietal lobe of brain. Both cases have the diagnosis supported by cardiac catheterization and angiography. The clinical, angiographic and pathologic characteristic of diverticulum and aneurysm of the heart are reviewed, and an attempt is made to clarify the concept of aneurysm and diverticulum of the heart.
Aneurysm*
;
Angiography
;
Brain
;
Cardiac Catheterization
;
Cardiac Catheters
;
Congenital Abnormalities
;
Coronary Vessels
;
Diagnosis
;
Diverticulum*
;
Heart
;
Heart Ventricles*
;
Myocardial Infarction
;
Ventricular Septum
8.Bentall Operation in a Patient with a Unicommissural Unicuspid Aortic Valve
Sung Joon PARK ; Jae Hoon LEE ; Eui Suk CHUNG
The Korean Journal of Thoracic and Cardiovascular Surgery 2019;52(5):368-371
A unicuspid aortic valve is a rare congenital malformation that frequently presents with valvular dysfunction and dilatation or aortic aneurysm, requiring combined aortic valve surgery and aortic repair. Some patients show severe valve calcification extending into the interventricular septum, possibly resulting in damage to the conduction system during debridement for valve replacement. We present a rare case of severe aortic stenosis with a unicommissural unicuspid aortic valve diagnosed by preoperative transesophageal echocardiography in a 36-year-old man. After composite graft replacement of the aortic valve, aortic root, and ascending aorta, a permanent pacemaker was placed because of postoperative complete heart block.
Adult
;
Aorta
;
Aortic Aneurysm
;
Aortic Valve Stenosis
;
Aortic Valve
;
Debridement
;
Dilatation
;
Echocardiography, Transesophageal
;
Heart Block
;
Heart Defects, Congenital
;
Humans
;
Transplants
9.Bilateral Coronary Artery-Right Ventricular Fistula in Newborn: Associated with Atrial Septal Defect.
Jo Won JUNG ; Jong Kyun LEE ; Jun Hee SUL ; Sung Kyu LEE ; Dong Gwan HAN
Korean Circulation Journal 1991;21(6):1259-1264
Bilateral coronary artery fistula is very uncommon congenital anomaly which occupy small percentage of all congenital coronary artery fistula. About 20% of the cases associated with additional congenital heart disease. And it may cause congestive heart failure, especially severely in neonate. We experienced a case of neonate who was 1 day-old-male with bilateral coronary artery-right ventricular fistula associated with atrial septal defect and congestive heart failure. The Patient was admitted because dyspnea, cyanosis since birth. 2D ecgicardiogram and cardiac catheterization revealed that a fistulous communicating ; forming a large aneurysm, was noted from bilateral coronary artery emptied into the right ventricle, and there was oxygen step-up in right ventricle.
Aneurysm
;
Cardiac Catheterization
;
Cardiac Catheters
;
Coronary Vessels
;
Cyanosis
;
Dyspnea
;
Fistula*
;
Heart Defects, Congenital
;
Heart Failure
;
Heart Septal Defects, Atrial*
;
Heart Ventricles
;
Humans
;
Infant, Newborn*
;
Oxygen
;
Parturition
10.Transesophageal Echocardiography: Technique, Anatomy and Clinical Applications.
Seung Sok CHUN ; Chong Mok YANG ; Ook Song CHUNG ; Man Young LEE ; In Soo PARK ; Jae Hyung KIM ; Kyu Bo CHOI ; Soon Jo HONG
Korean Circulation Journal 1991;21(2):263-277
Transesophageal echocardiography(TEE) is a new acoustic window to the cardiac structures and great vessels via retrocardiac esophagus. Because of the close relation between the esophagus and the heart, higher transducer frequencies can be applied, therefore leading to improved resolution and more accurate images than transthoracic echocardiography. We describe our experience with the first 353 awake patients. The procedure was well tolerated by the patients and associated with no major complications, within examination 10 to 20 minutes. Clinical diseases which appear to be suited for TEE includes 1) evaluation of native valve diseases, particulary mitral valve, pathologic valvular abnormalities and color Doppler regurgitant flows ; 2) assesment of prosthetic heart valves to better define malfunction and important pathologic associations ; 3) congenital heart disease, particularly atrial septal defect ; 4) endocarditis and detection of vegetations and complications ; 5) detection of thrombus and tumors, size, location, morphology, stalk ; and 6) aortic pathology including atherosclerosis, aneurysm and dissection. We conclude that transesophageal echocardiography is a new imaging technique that is rapidly evolving into a major tool for general cardiac imaging in a variety pathologic conditions and is a safe and useful tool in patients. Future advances in probe technology will continue to expand its applications.
Acoustics
;
Aneurysm
;
Atherosclerosis
;
Echocardiography
;
Echocardiography, Transesophageal*
;
Endocarditis
;
Equidae
;
Esophagus
;
Heart
;
Heart Defects, Congenital
;
Heart Septal Defects, Atrial
;
Heart Valves
;
Humans
;
Mitral Valve
;
Pathology
;
Thrombosis
;
Transducers