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1.
Kyobu Geka ; 75(9): 714-717, 2022 Sep.
Artigo em Japonês | MEDLINE | ID: mdl-36156522

RESUMO

A 73-year-old woman with multiple episodes of cerebral infarction was diagnosed with nonbacterial thrombotic endocarditis( NBTE) and antiphospholipid antibody syndrome. Transesophageal echocardiography revealed highly mobile tumors both in the mitral and the aortic valve, and the patient underwent aortic and mitral valve replacement. Pathologically, tumor of the mitral valve was a thrombus, and that of the aortic valve was a papillary fibroelastoma. Early after surgery, a recurrent thrombus was found in the left atrium, but no organ embolization ensued, and the patient had no adverse event for six months thereafter. Surgery is indicated only in limited cases of NBTE, because postoperative anticoagulation therapy is hard to manage and clinical outcome is poor.


Assuntos
Síndrome Antifosfolipídica , Endocardite , Trombose , Idoso , Anticoagulantes , Síndrome Antifosfolipídica/complicações , Síndrome Antifosfolipídica/patologia , Endocardite/complicações , Endocardite/diagnóstico por imagem , Endocardite/cirurgia , Feminino , Humanos , Valva Mitral/patologia , Trombose/diagnóstico por imagem , Trombose/etiologia , Trombose/cirurgia
2.
Kyobu Geka ; 75(6): 457-460, 2022 Jun.
Artigo em Japonês | MEDLINE | ID: mdl-35618692

RESUMO

A 55-year-old woman was diagnosed with Turner syndrome following amenorrhea at age 20. Since then, hormone replacement therapy has been used in the obstetrics and gynecology department, but follow-up for cardiovascular disease has not been performed. At age 44, she was taken to our hospital for the first time because of acute aortic dissection and rupture, and urgently underwent total arch replacement. At age 55, she needed aortic valve and ascending aortic replacements for aortic regurgitation, ascending aortic aneurysm, and heart failure caused by the bicuspid aortic valve. Cardiovascular manifestation in Turner syndrome patients is common, and close follow-up using imaging studies may predict emergency diseases that critically affect patient's life. Medical professionals should inform patients and families of the value of follow-up.


Assuntos
Aneurisma Aórtico , Dissecção Aórtica , Procedimentos Cirúrgicos Cardíacos , Síndrome de Turner , Adulto , Dissecção Aórtica/complicações , Dissecção Aórtica/diagnóstico por imagem , Dissecção Aórtica/cirurgia , Valva Aórtica/diagnóstico por imagem , Valva Aórtica/cirurgia , Procedimentos Cirúrgicos Cardíacos/efeitos adversos , Feminino , Humanos , Pessoa de Meia-Idade , Gravidez , Síndrome de Turner/complicações , Adulto Jovem
3.
Kyobu Geka ; 69(9): 792-5, 2016 Aug.
Artigo em Japonês | MEDLINE | ID: mdl-27476571

RESUMO

A 77-year-old woman presented with a 3-week history of low grade fever, appetite loss and dizziness. An electrocardiogram showed complete heart block. Echocardiography demonstrated severe aortic valve stenosis and a mass of probable vegetation 2 cm in diameter on the atrioventricular septum in the right atrium (RA), but no obvious intra-cardiac fistula. There was no growth of organism in blood cul tures. In the 4th week after admission, a harsh and continuous cardiac murmur was detected for the 1st time. Portable echocardiography revealed disappearance of the mass in the RA, and showed an intra-cardiac shunt from the left ventricle( LV) to RA. The shunt was closed by autologous pericardial patch form LV side and directly with mattress suture form RA side during the emergency operation. The aortic valve was replaced with bio-prosthetic valve (SJM Trifecta 19 mm). No organism was detected in the excised tissue, but antibiotics were continued for 2 months until a permanent pacemaker was inserted.


Assuntos
Insuficiência da Valva Aórtica/cirurgia , Endocardite/cirurgia , Idoso , Insuficiência da Valva Aórtica/etiologia , Procedimentos Cirúrgicos Cardíacos , Endocardite/complicações , Feminino , Humanos
4.
J Card Surg ; 27(3): 390-2, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22621721

RESUMO

Pentalogy of Cantrell is a rare congenital anomaly characterized by a combination of severe defects in the middle of the chest and abdomen including intracardiac defects. Survival rate after cardiac surgery is extremely low. We present a successful staged complete repair of an omphalocele, a ventricular septal defect and a sternal defect in a case of pentalogy of Cantrell.


Assuntos
Ectopia Cordis/cirurgia , Comunicação Interventricular/cirurgia , Hérnia Umbilical/cirurgia , Pentalogia de Cantrell/cirurgia , Esterno/cirurgia , Pré-Escolar , Ectopia Cordis/diagnóstico , Comunicação Interventricular/diagnóstico por imagem , Hérnia Umbilical/diagnóstico , Humanos , Lactente , Recém-Nascido , Masculino , Pentalogia de Cantrell/diagnóstico , Esterno/anormalidades , Ultrassonografia
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