Surgery for Aortic Valvular Disease with Congenital Bicuspid Aortic Valve | ||||||
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An increase of aortic valvular disease
associated with congenital bicuspid aortic valve is observed
due to the relative decrease of rheumatic valvular diseases.
A total of 24 patients with aortic valvular disease associated
with congenital bicuspid aortic valve underwent surgical treatment
at our institution during the period from January, 1997 to December,
1999. These 24 patients constituted 46.2% (24/52) of all cases
of surgical operations for aortic valvular disease. The age of
the patients ranged from 17 to 83 years (mean 62 years). They
consisted of 16 men (66.7%) and 8 women. Two patients had infective
endocarditis. The classification of congenital bicuspid aortic
valve was right-left cusp type in 15 patients (raphe+: 11), anterior-posterior
cusp type in 9 patients (raphe+: 9). We performed aortic valve
replacement in 22 patients, aortic root replacement in 1 patient
and aortic root remodeling in 1 patient in combination with mitral
valve plasty in 3 patients, coronary artery bypass grafting in
3 patients and closure of the atrial septal defect (ASD) in 1
patient. We detected ASD in 1 patient, ventricular septal defect
in 1 patient and high-posterior take-off right coronary artery
in 1 patient. Patients with stenosis often have a small aortic
annulus and severe post-stenotic aortic dilation. Preoperative
and intraoperative evaluation is important in cases of aortic
valvular disease associated with congenital bicuspid aortic valve. Jpn. J. Cardiovasc. Surg. 30: 59-62 (2001) |
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Beneficial Effects of Preoperative Coronary Angiography and Coronary Artery Revascularization in Patients Undergoing Surgery for Abdominal Aortic Aneurysm | |||||||||
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It is well known that patients with
abdominal aortic aneurysms (AAA) have a high incidence of coronary
artery disease (CAD), and that the major cause of death in patients
undergoing aneurysmectomy is acute myocardial infarction. A total
of 53 patients (mean age, 71 years) underwent elective repair
of AAA between January 1991 and November 1999. In an attempt
to reduce early and late mortality caused by myocardial infarction,
coronary angiography (CAG) was performed in all cases. Significant
CAD was found in 23 patients (43%), with triple vessel disease
in 1 patient (2%), double vessel disease in 5 patients (9%),
single vessel disease in 16 patients (30%) and left main in 1
patient (2%). Ten patients (19%) in whom CAD was detected by
CAG had no history of CAD and displayed no ischemic findings
on ECG. In 4 patients (8%), AAA repair was performed 2 (mean)
months after coronary artery bypass grafting (CABG). Percutaneous
transluminal coronary angioplasty (PTCA) was performed in 8 patients
(23%) 19 days (mean) prior to AAA surgery. No patient had a perioperative
myocardial infarction either following coronary revascularization
(CABG and PTCA) or AAA resection. Moreover, there was only one
operative death after abdominal aneurysmectomy (2%), in a patient
who was 70 years old with chronic hemodialysis and who died due
to multiple organ failure caused by uncontrollable adhesional
ileus. The results of this study emphasize the importance of
preoperative routine coronary angiography following coronary
artery revascularization to enhance the operative outcome of
AAA repair. Jpn. J. Cardiovasc. Surg. 30: 63-67 (2001) |
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A Successful Anatomical Reconstruction for Mycotic Abdominal Aortic Aneurysm with Infectious Abcess | ||||||
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Mycotic aortic aneurysm is a rare
disease which is caused by bacterial infection of the aortic
wall, grows rapidly with subsequent rupture and has high mortality.
We report a case of successful anatomical reconstruction for
mycotic abdominal aortic aneurysm with infectious abcess. A 59-year-old
man who was found to have an impending rupture of abdominal aortic
aneurysm underwent emergency anatomical reconstruction. At operation,
an active infectious abcess was noted around the abdominal aorta.
Successful management of this disease depends on early accurate
preoperative diagnosis, complete resection and debridment of
infected tissues, anatomical graft replacement and adjuvant antibiotic
chemotherapy. Jpn. J. Cardiovasc. Surg. 30: 68-70 (2001) |
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A Case of True Atherosclerotic Intercostal Aneurysm Diagnosed by Medical Examination | |||||||||
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Intercostal artery aneurysm is a rare disease, and is usually associated with aortic coarctation, trauma and infection. Until recently, diagnosis of the aneurysm had not been possible before rupture of aneurysm. However, recent advances in computed tomography (CT) and magnetic resonance imaging (MRI) have made it possible to diagnose this lesion. A 68-year-old man was admitted with an abnormal shadow on chest X-ray film. A chest CT scan showed an aneurysm beside the descending aorta, suggestive of intercostal artery aneurysm. Intraoperative inspection confirmed the diagnosis. The aneurysm was shown to be atherosclerotic in origin by postoperative histological examination. Jpn. J. Cardiovasc. Surg. 30: 71-73 (2001) |
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Coronary Artery Bypass Grafting without Cardiopulmonary Bypass and Percutaneous Coronary Angioplasty in a Patient with Cerebrovascular Stenosis | |||||||||
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Complete revascularization of the
coronary artery was performed in a 73-year-old man who had severe
stenosis of the bilateral subclavian and left vertebral arteries
and severe calcification of the ascending aorta. At first, we
performed CABG (coronary artery bypass grafting) on the LAD (left
anterior descending artery) and the RCA (right coronary artery)
without cardiopulmonary bypass. In-situ GEA (gastroepiploic
artery) was anastomosed to the LAD and SVG (saphenous vein graft)
was anastomosed to 4PD (4 posterior descending artery) of the
RCA. The right brachiocephalic artery was selected as the site
of the proximal anastomosis of the SVG. A Palmaz-Schatz stent
was then held in place in the LCX (left circumflex artery) postoperatively.
The combination of CABG without cardiopulmonary bypass and PTCA
was a safe method for preventing cerebrovascular complications
in a patient with a severely calcified artery. Jpn. J. Cardiovasc. Surg. 30: 74-76 (2001) |
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A Case of Surgical Treatment for Type A Aortic Dissection Associated with Proximal Descending Thoracic Aortic Aneurysm | ||||||||||||
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A 63-year-old man suffered from
type A acute aortic dissection associated with descending thoracic
aortic aneurysm and coronary stenosis. He was treated surgically
49 days after onset of acute aortic dissection. Deep hypothermic
selective cerebral perfusion was carried out for brain protection.
It revealed the aneurysm, 51mm in diameter, located just distal
to the aortic arch, and an intimal tear of the dissection located
posterior wall of aneurysm. The total arch was replaced with
24mm vascular graft and CABG (LITA-to-seg.8) was carried out.
The postoperative course was uneventful and he was discharged
on the 18th postoperative day. Jpn. J. Cardiovasc. Surg. 30: 77-79 (2001) |
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Successful Surgical Closure of a Coronary Sinus Atrial Septal Defect Using a Heart-Shaped Patch | ||||||
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A 21-year-old man with coronary
sinus atrial septal defect (ASD) was treated successfully. This
case had been diagnosed as an ASD without a lower margin preoperatively
but we confirmed this to be a coronary sinus ASD intraoperatively,
and this case was classified as partially unroofed coronary sinus
without PLSVC. The diagnosis of coronary sinus ASD before operation
is sometimes difficult. Therefore we should pay attention to
the location of the defect and the dilated coronary sinus in
echocardiography, and the course of the cardiac catheter entering
into the left atrium, for a correct diagnosis. In this case,
the defect was located in the vicinity of the ostium of a large
coronary sinus, therefore we could close the defect between the
CS and the LA using a heart-shaped patch without any damage to
the AV node. Jpn. J. Cardiovasc. Surg. 30:80-82(2001) |
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A Case of Coarctation of Descending Mid-Thoracic Aorta Caused by Fibromuscular Dysplasia | ||||||
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A rare case of descending thoracic
aortic coarctation caused by fibromuscular dysplasia is reported.
A 74-year-old woman was referred to our institution because of
congestive heart failure, hypertension, acute renal failure and
pressure gradient between upper and lower extremities. Aortography
revealed 90% stenosis of the descending mid-thoracic aorta. Descending-descending
aortic bypass was performed under femoro-femoral partial cardiopulmonary
bypass. The post-operative course was uneventful and the pressure
gradient across the coarctation was disappeared. The patient
discharged on the 28th postoperative day without any problems.
The pathohistological findings revealed fibromuscular dysplasia
in the media and intima of the aortic wall. Jpn. J. Cardiovasc. Surg. 30: 83-85(2001) |
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A Third CABG Procedure(Axillo-Coronary Bypass) Using the MIDCAB Technique | |||||||||
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A 77-year-old man had undergone
CABG (coronary artery bypass grafting) (SVGs (saphenous vein
grafts) to LAD (left anterior descending coronary artery), OM
(obtuse marginal) and RCA (right coronary artery)) 15 years previously.
Three years previously, he underwent CABG again (LITA (left internal
thoracic artery)-OM, RGEA (right gastroepiploic artery)-RCA)
due to recurrence of angina pectoris, but there was no evidence
of graft disease in the SVG to the LAD. Six months before the
present procedure, graft disease developed in the SVG to the
LAD and caused unstable angina pectoris. Therefore, the left
axillary artery was bypass grafted to the coronary artery (LAD)
using SVG without cardiopulmonary bypass by means of the MIDCAB
(minimally invasive direct coronary artery bypass) technique.
The patient has had no angina pectoris subsequently. Postoperative
angiography revealed that the graft was patent. The axillo-coronary
(LAD) bypass appears to be a useful procedure for re-revascularization
to the LAD in patients with no available arterial graft, such
as ITA (internal thoracic artery) or RGEA. Jpn. J. Cardiovasc. Surg. 30: 86-88 (2001) |
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A Case of Descending Aortic Rupture due to Blunt Chest Trauma | ||||||
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We report a case of rupture of the
thoracic descending aorta due to blunt chest trauma. An 18-year-old
man was transferred to our hospital after a car accident. He
was in a state of shock. The admission chest X-ray film demonstrated
mediastinal widening and blurring of the aortic arch. Chest and
abdominal helical CT scan showed left hemothorax, pseudoaneurysm,
and hematoma of the cervix, mediastinum, and retroperitoneal
space. We diagnosed rupture of the thoracic descending aorta
without other injuries. An emergency operation was performed
under partial cardiopulmonary bypass with systemic heparinization.
The descending aorta had completely lost its continuity. Graft
replacement was performed with a collagen-sealed woven Dacron
graft. The postoperative course was uneventful. We suggest that
high awareness and a systematic approach are needed to diagnose
traumatic aortic rupture, and that enhanced helical CT scanning
is helpful for diagnosis and management strategy. Jpn. J. Cardiovasc. Surg. 30: 89-91 (2001) |
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A Case Report of Abdominal Aortic Aneurysm Associated with Crossed-Fused Ectopia of the Kidney | ||||||
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A rare case of abdominal aortic
aneurysm associated with crossed-fused ectopic kidney in a 74-year-old
man is reported. On enhanced CT scans, the maximum diameter of
his infrarenal aortic aneurysm was 55mm, and he lacked a right
kidney. A crossed ectopic kidney was fused to the lower part
of the left kidney. On preoperative examinations, only one feeding
artery to the ectopic kidney separated from the right common
iliac artery. However, laparotomy confirmed the presence of three
aberrant renal arteries, the middle one of which was very slim.
Aneurysmectomy and a bifurcated artificial graft replacement
was performed. After proximal anastomosis, the two larger aberrant
renal arteries were reconstructed under renal protection with
intermittent infusion of cold Ringer's solution. The smallest
aberrant renal artery was ligated. Postoperatively, this patient
recovered without any complications. In operations for abdominal
aortic aneurysm associated with renal anomaly including ectopic
kidney, horseshoe kidney, and pelvic kidney, it is important
to elucidate the anatomy of aberrant renal arteries preoperatively,
and reconstruct as many of these arteries as possible. This report
is apparently the fourth on abdominal aortic aneurysm associated
with crossed ectopic kidney. Jpn. J. Cardiovasc. Surg. 30: 92-94 (2001) |
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A Case of Non-Anastomotic False Aneurysm of Late Fiber Deterioration in Dacron Graft | ||||||
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Dacron prostheses are the most widely
used grafts in replacement procedures for abdominal aortic aneurysms,
but they are not perfect grafts. We encountered a rare case of
late graft complication. A 66-year-old man was admitted to our
hospital with a pulsatile mass in an abdominal operation scar.
He had received placement of a Y-shaped Cooley double velour
knitted Dacron graft 18 years previously. Computed tomography
and angiography demonstrated graft dilatation and an aneurysm.
After resection of the graft aneurysms, the operative findings
showed a non-anastomotic aneurysm formation due to longitudinal
division near the graft guideline. In this case, this graft failure
may have been due to the deterioration of the filter of the Dacron
prosthesis itself. Therefore it is important to perform careful
long-term follow-up in patients with implanted Dacron arterial
prostheses. Jpn. J. Cardiovasc. Surg. 30: 95-98 (2001) |
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A Case of Simultaneous Surgery for Distal Aortic Arch Aneurysm Complicated by Left Ventricular Aneurysm | ||||||
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A 72-year-old man consulted a local
physician due to an episode of loss of consciousness. When chest
CT was performed after amelioration of symptoms, aneurysmal dilation
was detected at the distal aortic arch. On CT, a distal aortic
arch aneurysm appeared to be a sacciform aneurysm measuring 55mm
in maximum diameter. In addition, coronary arteriography demonstrated
complete obstruction of left anterior descending branch #6, while
left ventriculography demonstrated left ventricular aneurysm
due to old myocardial infarction. The left ventricular end-diastolic
volume was increased to 285ml, and the end-systolic volume was
increased to 224ml. Moreover, the left ventricular ejection fraction
was markedly decreased to 21%. The distal aortic arch aneurysm
was treated by total aortic arch replacement. Considering the
postoperative development of cardiac failure, the left ventricular
aneurysm was simultaneously treated by endoventricular patch
plasty, the so-called Dor operation. The postoperative course
of this patient was satisfactory, because the end-diastolic volume
was decreased to 241ml, and the end-systolic volume was also
decreased to 147ml. Furthermore, the left ventricular ejection
fraction was increased to 39%, demonstrating an improvement in
left ventricular function. In Japan, there have not been any
reports describing simultaneous surgery for thoracic aortic aneurysm
complicated by left ventricular aneurysm. Therefore, the present
study reports the course of this patient, including the indications
of endoventricular patch plasty. Jpn. J. Cardiovasc. Surg. 30: 99-102 (2001) |
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Management of Inguinal Vascular Graft Infection by Lateral Femoris Axillo-Popliteal Bypass | |||
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A 81-year-old man was referred to
our hospital for treatment of a skin ulcer of the right anterior
crus. After 2 months left common femoral artery-right popliteal
artery bypass, graft infection was occurred and methicillin-sensitive
Staphylococcus aureus was found in the bacterial culture.
The wound was extended in order to decide the extent of graft
infection, but graft healing was totally insufficient. All of
the graft was excised, and right axillo-popliteal bypass using
8mm Bionit graft was performed. The graft was passed through
lateral femoral. Thus, in this case the graft excision was necessary,
but major amputation could be avoided by successful revascularization. Jpn. J. Cardiovasc. Surg. 30: 103-105 (2001) |
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A Case of Simultaneous Operation for Unstable Angina and Leriche's Syndrome with a Large Arterial Collateral to the Lower Limb | |||
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A 52-year-old male with unstable
angina after acute myocardial infarction, and Leriche's syndrome
was referred to our hospital for intensive care. He had a history
of diabetes. Coronary angiography demonstrated a 75% stenosis
of the LMT in association with a 90% stenosis of the LAD, 75%
stenosis of the LCX and 99% stenosis of the RCA. Aortography
revealed an arterial occlusion extending from the infrarenal
aorta to both common iliac bifurcations. Both internal thoracic
arteries were well developed as collateral pathways to external
iliac arteries. With concomitant Y graft replacement of the abdominal
aorta, two large internal thoracic arterial conduits and the
right gastroepiploic artery were grafted to the coronary artery.
This procedure was useful for protection of limb ischemia, in
addition to producing a route for insertion of an intraaortic
balloon pumping catheter. Jpn. J. Cardiovasc. Surg. 30: 106-109 (2001) |
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