Naoki Wada | Yukihiro Takahashi | Makoto Ando |
Toshio Kikuchi | Hitomi Boku* |
Hiroki Hayashi | Yukihiro Takahashi | Makoto Ando |
Masahito Yamashiro | Keima Nagamachi | Toshio Kikuchi |
Hitoshi Kasegawa |
Tsutomu Sugimoto | Kazuo Yamamoto | Shinpei Yoshii |
Satoshi Tanaka | Norihiko Saito | Chizuo Kikuchi |
Kenji Aoki | Atsushi Kuwabara | Shigetaka Kasuya |
Jiro Esaki | Motoaki Ohnaka* | Shinya Takahashi* |
Kotaro Shiraga** | Nobushige Tamura* | Tatsuhiko Komiya* |
Saihou Hayashi | Masafumi Sueshiro | Tomokuni Furukawa |
Takehiko Furusawa | Kazunori Nishimura | Nobuyuki Yanagiya |
Seiji Kinugasa | Fumitaka Isobe | Keiji Iwata |
Tadahiro Murakami | Yukiya Nomura | Motoko Saito |
Masatoshi Hata | Manabu Motoki |
A Case of Marfan's Syndrome with Acute Aortic Dissection during Pregnancy | |||||||||
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We present a case of Marfan's syndrome
with acute aortic dissection during the trimester of her pregnancy,
who underwent a Bentall operation 2 days after emergency cesarean
section. A 24-year-old woman during the 31st week of pregnancy
visited our emergency room due to sudden onset of chest and back
pain, though she had no abnormality until this event. Because
of her tall height, spider fingers, positive wrist sign, visual
disorder and scoliosis, she was given a diagnosis of Marfan's
syndrome. Enhanced CT and cardiac ultrasonography revealed that
she was suffering from acute aortic dissection with annulo-aortic
ectasia. Since it was difficult for her to continue with her
pregnancy, she underwent emergency cesarean section and gave
birth to a male baby weighted 1,706g. Although there was little
likelifood of early thrombus formation in the false lumen or
significant aortic regurgitation indicating an emergency operation,
fear of massive bleeding from her uterus and the exfoliated surface
of the placenta after cesarean section required an observation
period of 2 days. We performed a Bentall operation successfully
after careful sedation, ventilation and blood pressure control
for 2 days. Jpn. J. Cardiovasc. Surg.34: 116-119 (2005) |
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A Case of Isolated Right Common Iliac Aneurysm with Arteriovenous Fistula | |||
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We report a case of arteriovenous
fistula (AVF) secondary to spontaneous rupture of the right common
iliac aneurysm into the right common iliac vein. In February
2003, an 81-year-old woman was admitted with dyspnea. Diuretics
and digitalis were given under a provisional diagnosis of primary
heart failure. Afterwards the heart failure turned out to be
high output failure due to AVF. In June the patient complained
of swelling of her right leg and was referred to our department.
Ultrasonography to determine deep vein thrombosis of the right
femoral vein revealed a dilatation of the left femoral vein,
but there was no thrombosis. A pulse Doppler detected an arterial
blood flow signal during early systolic pulse in the right femoral
vein, confirming the suspicion of an AVF in abdominal cavity
near this location. A pulsatile mass associated with bruit and
thrill was palpable in the lower abdomen. Digital subtraction
angiography showed a 50mm aneurysm of the right common iliac
artery. Rapid visualization of the inferior vena cava and retrograde
opacification of the right iliac vein indicated the presence
of an AVF between the common iliac artery and vein. Operation
was done by laparotomy on June 24, 2003. An occlusive balloon
catheter was inserted from the right femoral vein and the balloon
was dilated to patch the fistula before opening the aneurysm.
After clamping the proximal and distal arteries the aneurysm
was opened. By this maneuver there was no bleeding from the fistula.
The AVF was closed from inside the aneurysm by 3 interrupted
4-0 monofilament sutures. The aneurysm was replaced with a prosthetic
graft (Hemashield 8mm). The post-operative course was uneventful.
The lower limb edema subsided and heart failure improved. Jpn. J. Cardiovasc. Surg. 34: 120-123 (2005) |
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A Case of Pacemaker (PM) Contact Sensitivity due to Silicon Allergy Which Occurred 24 Years after PM Implantation | ||||||
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A 44-year-old man underwent implantation
of a DDD pacemaker for third degree heart block at age 20. The
cutaneous pocket for the pulse generator was situated in the
left pectoral region. He visited our hospital because of skin
ulcer over the pacemaker without any other complaint such as
fever or pain. The patient received a new DDD pacemaker system
in the right pectoral region and old pacing leads were translocated
under the pectoral muscle. However, right pectoral skin ulcer
appeared 1 month later. Patch tests revealed a positive reaction
to silicon. Wrapping of the pacemaker with a polytetrafluoroethylene
(PTFE) sheet proved to be effective. Jpn. J. Cardiovasc. Surg. 34: 124-126 (2005) |
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Dissected Abdominal Aortic Aneurysm in a 24-Year-Old Female―Minimally Invasive Right Retroperitoneal Approach― | |||||||||
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A 24-year-old woman with an abdominal
aortic aneurysm (AAA) caused by mucoid medial degeneration of
the aortic wall in the absence of Marfan syndrome is reported.
She required a Y-shaped graft replacement of the abdominal aorta
through a minimal incision and recovered successfully. Jpn. J. Cardiovasc. Surg. 34:127-129 (2005) |
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Simultaneous Surgery for Angina Pectoris and Abdominal Aortic Aneurysm with Bilateral Iliac Artery Occlusion in a Chronic Hemodialysis Patient | ||||||
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A74-year-old man with renal failure
had been treated with maintenance hemodialysis for 1.5 years
at another hospital. The patient had an abdominal aortic aneurysm,
bilateral iliac artery occlusion and coronary artery stenosis
with a lesion in the left main trunk, but had been under observation
because of the high risk of surgery. The patient elected to have
surgery and was admitted to our hospital. We performed simultaneous
surgery for severe coronary artery stenosis and abdominal aortic
aneurysm with a maximum diameter of 85mm. The postoperative course
was generally uneventful, but the patient required treatment
of arrhythmia. We conclude that simultaneous surgery for angina
pectoris and abdominal aortic aneurysm is feasible even in hemodialysis
patients. It is important to pay attention to arrhythmia in the
management of such patients, especially those with decreased
cardiac function. Jpn. J. Cardiovasc. Surg. 34: 130-133 (2005) |
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A Case of Esophageal Stenosis with Descending Aortic Elongation (Dysphagia Aortica) | ||||||
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We report a case of dysphagia caused
by compression of the esophagus by the nonaneurysmal tortuous
descending aorta (dysphagia aortica). A 69-year-old woman was
admitted suffering from dysphagia. Esophagoscopy showed esophageal
stenosis caused by pulsatile and extramural compression. Esophagography
and aortograms also showed that the nonaneurysmal tortuous descending
aorta compressed the esophagus in an anteromedian direction.
To avoid the esophageal ulcer and the aortoesophageal fistula,
resection of the tortuous aorta and a Dacron graft replacement
was performed. After operation compression of the esophagus was
released and her complaint improved. Jpn. J. Cardiovasc. Surg. 34: 134-136 (2005) |
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Coronary Artery Bypass Graft in a Patient Who Had Increased Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) Levels after Treatment with Heparin | ||||||
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Cardiac surgery using heparin was
performed in a patient in whom AST and ALT had been increased
due to continuous drip infusion of heparin sodium. Here, we report
postoperative changes in AST and ALT in the patient. The patient
was a 59-year-old man with a past medical history of left internal
carotid artery constriction and right cerebral infarction. Because
of his previous medical history, continuous drip infusion of
heparin was initiated upon discontinuation of preoperative antithrombotic
agents. AST and ALT increased, but returned to normal levels
when heparin was discontinued. Heparin was used to avoid aggravation
of the symptoms, and bypass of 3 branches was performed with
pulsation. Postoperative respiration and circulatory dynamics
were stable, and the courses of AST and ALT were similar to those
after general surgery, without abnormally high levels. Although
the cause of heparin-induced increases in AST and ALT is unknown,
the absence of postoperative increases may have been due to transient
use at a high dose and neutralization by protamine. Jpn. J. Cardiovasc. Surg.34: 137-139 (2005) |
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A Giant Right Atrial Myxoma with Lung Carcinoma Detected by Syncope | ||||||
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A 75-year-old man was referred to
our hospital with dyspnea on effort, recurrent attacks of loss
of consciousness and abnormal shadow on chest X-ray film. Computed
tomographic scan confirmed a 1.5×2.0cm mass with slight spiculation
in the right lower lobe (S6) and revealed an ovoid right atrial
mass. Transthoracic echocardiography showed that the giant mass
which filled most of the right atrium had no mobility. Coronary
angiography revealed clusters of new vessels which originated
from the atrial branches of the circumflex coronary artery. A
T1-weighted MRI scan demonstrated that the mass was isointense
relative to the adjacent myocardium. We considered that performing
cardiac surgery prior to pulmonary resection, as in a staged
procedure, would have advantages in morbidity. We first performed
removal of the right atrial tumor which was a 6.8×5.5×4.5cm shiny
mass attached to the interatrial septum. Histological examination
of the mass confirmed the diagnosis of cardiac myxoma. Three
months later, right S6 segmentectomy was carried out
using thoracoscopy and the tumor was finally diagnosed as squamous
cell carcinoma. We have followed the patient for about 10 months
after the first operation and there is no evidence of tumor recurrence
and no more syncopic attacks. Jpn. J. Cardiovasc. Surg. 34: 140-143 (2005) |
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Acute Anterolateral Papillary Muscle Rupture Following Successful Percutaneous Coronary Intervention and Emergent Mitral Valve Replacement | ||||||
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A72-year-old woman complaining of
orthopnea was admitted with cardiogenic shock. Her systolic blood
pressure was only 66mmHg and electrocardiogram showed high lateral
myocardial infarction. Transthoracic echocardiogram showed severe
mitral regurgitation and disruption of the anterolateral papillary
muscle. After orotracheal intubation and intraaortic balloon
pumping (IABP), coronary angiogram was performed and an occlusion
of the entrance of circumflex artery (#11) was diagnosed. Percutaneous
coronary intervention was done successfully and emergency mitral
valve replacement was performed using a St. Jude Medical prosthetic
valve preserving the posterior mitral valve leaflet and mitral
apparatus. Her postoperative recovery was entirely uneventful
and she was followed up as an outpatient. Acute anterolateral
papillary muscle rupture is a rare complication of acute myocardial
infarction (AMI), although left coronary artery disease is associated
with it and immediate recanalization is an important issue to
rescue the patient. Jpn. J. Cardiovasc. Surg. 34: 144-147 (2005) |
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A Case of Ruptured Abdominal Aortic Aneurysm with Intraoperative Cardiac Arrest | |||
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We report a case of emergency operation for ruptured abdominal aortic aneurysm with intraoperative cardiac arrest. The patient was a 71-year-old man with a past history of CABG and total gastrectomy. A transperitoneal approach was used for operation. Intraoperatively, a large retroperitoneal hematoma and intestinal adhesion were found. This large retroperitoneal hematoma increased, followed by cardiac arrest. Immediately left thoracotomy, direct cardiac massage and digital compression to the descending aorta were performed. After aneurysmal opening, an occlusion balloon was inserted in descending aorta. The infrarenal aorta was exposed and clamped. Cardiopulmonary resuscitation was successful. The aneurysm was replaced with a bifurcated artificial vessel and distal anastomosis to the bilateral femoral arteries. There were no signs of cardiac or renal failure in the early postoperative period. The postoperative recovery was successful. Jpn. J. Cardiovasc. Surg. 34: 148-151 (2005) |
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Coronary Artery Bypass Grafting in Situs Inversus Totalis | ||||||
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Cardiovascular surgery in situs
inversus totalis (SIT) is unusual. We report a case of coronary
artery bypass grafting (CABG) in SIT. A 67-year-old man with
unstable angina pectoris was admitted to our hospital. Coronary
arteriography demonstrated three-vessel disease in the mirror-image
heart. CABG with 4 distal anastomosis was carried out with conventional
methods. Careful observation based on complete understanding
for preoperative images could minimize operative difficulties
caused by mirror-image heart. Jpn. J. Cardiovasc. Surg. 34: 152-155 (2005) |
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A Case of Ascending Aorta Pseudoaneurysm due to a Freestyle-Valve Free-Wall Fistula after a Modified Bentall Procedure with the Button Technique | |||||||||
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We encountered a case of ascending
aorta pseudoaneurysm due to a Freestyle-valve free-wall
fistula after a modified Bentall procedure with the button
technique. A 60-year-old man with Marfan's syndrome who
contracted annuloaortic ectasia presented with the onset
of Stanford A type acute aortic dissection 3 years ago.
The patient underwent aortic root replacement with a Freestyle-valve
and ascending and hemi-arch aortic replacement. Thirty-seven
months after this operation the patient was re-operated
because of pseudo-ascending aorta aneurysm. The cause
of the pseudo-aneurysm was a fistula of the Freestyle-valve
free-wall and the left coronary artety (LCA) ostial reconstruction
component. The fistula was repaired by direct closure
with pledgets. The patient was discharged from the hospital
24 days after the operation. Jpn. J. Cardiovasc. Surg. 34: 156-158 (2005) |
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Keita Kikuchi | Haruo Makuuchi | Hiroshi Murakami |
Takamaro Suzuki | Takashi Ando | Makoto Ohno |
Hirokuni Ono | Kiyoshi Chiba | Shinichi Endo* |