1.A Case of Healed Aortic Prosthetic Valve Endocarditis Accompanied by an Aneurysm of the Sinus of Valsalva Treated with the Aortic Valve Replacement of Perceval
Makoto TAKEHARA ; Sanae TOMOTSUKA ; Shinichi TSUMARU ; Takeshi SHIMAMOTO
Japanese Journal of Cardiovascular Surgery 2023;52(2):88-92
An 87-year-old woman underwent AVR (CEP 21 mm) for aortic stenosis at age 73 years. Fourteen years later, she was treated with antibiotics for mediastinal abscess, which showed a tendency to shrink and inflammation improved. At that time, no vegetation or aortic regurgitation was observed. Eight months later, the patient was brought to the emergency room with a complaint of respiratory distress. After close examination, a severe transvalvular leakage was found at the aortic valve position. No vegetation was found. Enhanced chest computed tomography (CT) showed an aneurysm of the left sinus of Valsalva. The diagnosis of healed aortic prosthetic valve endocarditis with an aneurysm of the sinus of Valsalva was made. The CEP valve was removed at surgery, and the valve leaflet corresponding to the right coronary cusp was destroyed. The left sinus of Valsalva was dilated and a Perceval was implanted. The patient was doing well postoperatively, but a pacemaker was implanted due to atrioventricular dissection. Transthoracic echocardiography confirmed that there was no problem with prosthetic valve function at the aortic valve position, and CT showed a reduction of aneurysm of the left sinus of Valsalva. The patient was discharged from the hospital on the 30th postoperative day. Aortic valve replacement with Perceval is effective in high-risk cases of prosthetic valve endocarditis.
2.A Case of Partial Remodeling for Type A Aortic Dissection Requiring Aortic Root Reconstruction
Yoshimasa FURUICHI ; Tatsuhiko KOMIYA ; Takeshi SHIMAMOTO ; Michihito NONAKA ; Takehiko NONAKA ; Junya KITAURA ; Taiyo JINNO ; Atsushi SUGAYA
Japanese Journal of Cardiovascular Surgery 2020;49(3):133-137
A 48-year-old woman was admitted to our hospital with exertional dyspnea and lower leg edema since 2 months previously. Echocardiogram presented dilation of Valsalva sinus, severe AR (aortic regurgitation) and a supra-annular flap. Enhanced cardiac cycle-gated computed tomography revealed Stanford type A aortic dissection. Primary entry was found just above the aortic valve, the right coronary artery branched from the false lumen, and the commissure between the right and non-coronary cusps was detached. The left coronary artery branched from the true lumen. The false lumen was all patent to the bilateral bifurcations of the common iliac artery. We performed valve sparing partial root remodeling, right coronary artery bypass and total arch replacement after the heart failure management. The operation, cardiopulmonary bypass, aortic cross clamp and selective cerebral perfusion times were 402, 234, 167 and 109 min, respectively. The postoperative course was uneventful, and the patient was discharged 12 days after the operation without any complication. Postoperative CT revealed a well-shaped Valsalva and complete thrombosis of the false lumen on the thoracic aorta. Aortic regurgitation completely disappeared according to a postoperative echocardiogram.
3.Determination of Clamp Site with Reference to a Cerebral Blood Flow Monitoring System in a Patient with a Right Subclavian Artery Aneurysm Complicated by Right Internal Carotid Artery Occlusion
Taiyo JINNO ; Hiroshi TSUNEYOSHI ; Jiro SAKAI ; Takeshi SHIMAMOTO ; Tatsuhiko KOMIYA
Japanese Journal of Cardiovascular Surgery 2019;48(6):433-437
A 66-year-old man was referred to our hospital for the treatment of a right subclavian artery aneurysm. Computed tomography showed a 35-mm aneurysm in the right subclavian artery, and occlusion of the right internal carotid artery. A surgical approach with maintenance of intracranial blood flow was required. During anastomosis of the graft to the native vessel, we clamped the distal and proximal portions of the right subclavian artery, to maintain the blood flow of the right common carotid artery. The INVOS® cerebral oximeter (Somanetics Corp., Troy, MI, USA) was useful in determining the clamping site and surgical strategy. The procedure was completed without complications, and the patient was discharged from the hospital on postoperative day 8 following a good clinical course.
4.A Severe Aortic Stenosis and Coronary Calcifications in Alkaptonuria
Osamu TOMINAGA ; Tatsuhiko KOMIYA ; Takeshi SHIMAMOTO ; Michihito NONAKA ; Jiro SAKAI ; Junya KITAURA ; Yoshimasa FURUICHI ; Taiyo JINNO ; Atsushi SUGAYA
Japanese Journal of Cardiovascular Surgery 2019;48(2):107-110
Alkaptonuria is a rare genetic disease, in which amino acids and tyrosine cannot be processed. A 72-year-old man with a history of aortic valve stenosis presented with coronary 3-vessel disease. Intraoperative findings included ochronosis, which is pigmentation caused by the accumulation of homogentistic acids in connective tissues, or on the severely calcified aortic valve, the intima of the aorta, and the coronary arteries. The pigmented region of the coronary arteries had significant stenosis. Aortic valve replacement and coronary artery bypass were performed. From these findings and his past history of arthritis, we diagnosed alkaptonuria. The patient had an uneventful recovery.
5.Stentgraft Treatment for Inflammatory Aortic Aneurysm of Thoracic Aorta in Behçet's Disease
Osamu TOMINAGA ; Tatsuhiko KOMIYA ; Hiroshi TSUNEYOSHI ; Takeshi SHIMAMOTO ; Toshifumi HIRAOKA ; Jiro SAKAI ; Kenji WADA ; Yuka FUJIMOTO ; Yoshimasa FURUICHI
Japanese Journal of Cardiovascular Surgery 2018;47(1):31-35
A 71-year-old man with Behçet's disease was admitted to our hospital for treatment of a thoracic aortic aneurysm. On admission, there was marked inflammatory response, but blood culture was negative and there was no significant accumulation of gallium scintigraphy. The aorta was shaggy and there were two aneurysms in the descending aorta. We performed endovascular aortic repair for this aneurysm in consideration of the inflammatory aortic aneurysm. After treatment, the patient had paraparesis, however he underwent physical rehabilitation to regain function. He was followed up for 1 year and remains in good clinical condition without anastomotic aneurysm, dilatation or aneurysm at another site.
6.Congenital Hypoplasia of the Left Main Coronary Artery Treated with Off-Pump Coronary Artery Bypass Grafting
Ken Yamanaka ; Tatsuhiko Komiya ; Hiroshi Tsuneyoshi ; Takeshi Shimamoto
Japanese Journal of Cardiovascular Surgery 2016;45(2):73-75
We encountered left main coronary artery hypoplasia in a 14-year-old boy. He had a history of syncope after exercise. Computed tomography revealed hypoplasia of the left main coronary artery and the syncope on exertion was diagnosed as due to myocardial ischemia. We performed off-pump coronary artery bypass (OPCAB) graft using the left internal thoracic artery. The postoperative course was uneventful and chest symptoms were not recognized in daily life. Left main coronary artery hypoplasia is rare, but is associated with adverse cardiac events, including sudden cardiac death. In cases like this, coronary artery bypass graft is indicated.
7.A Successful Case of Tricuspid Valve Replacement for Acute Right Heart Failure
Tomonori Koga ; Tatsuhiko Komiya ; Hiroshi Tsuneyoshi ; Takeshi Shimamoto
Japanese Journal of Cardiovascular Surgery 2015;44(2):74-78
A 75-year-old woman presented with dyspnea, and was admitted urgently on a diagnosis of concurrent acute cardiac insufficiency. Because of her low blood pressure and respiratory failure, care was started in the intensive care unit. A transthoracic echocardiogram (TTE) showed severe tricuspid regurgitation (TR). We concluded that her cardiogenic shock was caused by acute right heart failure with severe TR and therefore carried out emergency surgery. We noted expansion of the tricuspid valve ring and shortening of the tendinous cord, and the leaflet was pulled into the right ventricle side. Initially we attempted a tricuspid annuloplasty (TAP), but it proved difficult to control the TR. We therefore performed a tricuspid valve replacement (TVR). The patient was moved from the intensive care unit to a general ward 10 days after the operation, and to another hospital 26 days later.
8.Successful Treatment of Prosthetic Graft Infection 7 Years after Ascending Aorta Replacement and Aortic Root Replacement with a Freestyle Stentless Valve
Jiro Sakai ; Tatsuhiko Komiya ; Hiroshi Tsuneyoshi ; Takeshi Shimamoto
Japanese Journal of Cardiovascular Surgery 2015;44(3):137-140
A 62 year-old man presented with severe septic shock complicated by prosthetic graft infection, 7 years after aortic root replacement with a Freestyle stentless valve and graft replacement of the ascending aorta. We initially managed the patient with antimicrobial therapy for 2 months and subsequently surgery was performed, replacing the infected aortic graft with rifampicin-bonded prostheses, and added omentopexy. The infection was cured and has not recurred.
9.Successful Medical Treatment of Prosthetic Valve Endocarditis with a Perivalvular Abscess
Chikara Ueki ; Takeshi Shimamoto ; Genichi Sakaguchi ; Tatsuhiko Komiya
Japanese Journal of Cardiovascular Surgery 2012;41(1):21-24
A 68-year-old man visited our hospital with a high fever with chills 4 years after aortic valve replacement. Streptococcal species were cultured with a venous blood culture. An echocardiogram and a cardiac computed tomography (CT) scan revealed a perivalvular abscess (11 mm×15 mm). Because his prosthetic valve functioned well, he was treated with intravenous ampicillin and gentamicin. Cardiac CT scan performed at 6 weeks showed the perivalvular abscess to have disappeared and he was discharged from the hospital. He is free from recurrence of the abscess 20 months after the initiation of therapy.
10.A Case of Recurrent Rhabdomyosarcoma 11 Years after Radical Surgical Resection
Keisuke Watadani ; Takeshi Shimamoto ; Genichi Sakaguchi ; Nobushige Tamura ; Tatsuhiko Komiya
Japanese Journal of Cardiovascular Surgery 2011;40(4):184-187
The prognosis of rhabdomyosarcoma is poor, and its estimated survival is less than year even after radical resection. We report a patient with recurrent rhabdomyosarcoma 11 years after obtaining remission by radical surgical resection and chemotherapy.


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