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systolic murmurs/verenvuoto

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ArtikkelitKliiniset tutkimuksetPatentit
Sivu 1 alkaen 55 tuloksia

Occult gastrointestinal bleeding due to acquired von Willebrand syndrome in a patient with hypertrophic obstructive cardiomyopathy.

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A 69-year-old woman presented with a harsh systolic murmur and severe anemia. Echocardiography demonstrated hypertrophic obstructive cardiomyopathy with a peak pressure gradient of 154 mmHg. Endoscopic examinations disclosed an angiodysplasia and multiple diverticula in the colon, but no active

[Presented with subarachnoid hemorrhage and then blood culture negative infective endocarditis: a case report and literature review].

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The patient, a 43-year-old man, had paroxysmal headache three months ago, and he had complained the left occipital sharp pain, which could be alleviated by itself, with alalia and the right side of the upper limb numbness. Head computed tomography (CT) revealed a left temporal lobe intraparenchymal

Hemorrhagic myocardial infarction complicated by free wall-rupture: a case associated with unusual clinical features following intravenous thrombolytic therapy.

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A patient is described who developed a systolic murmur soon after she was administered intravenous thrombolytic therapy for acute myocardial infarction. She died and autopsy revealed extensive hemorrhagic myocardial infarction and a free-wall rupture. A review of the literature suggests that this

[Pulmonary hypertension in hereditary haemorrhagic teleangiectasia (Rendu-Osler-Weber disease). Progression over 10 years].

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METHODS 10 years ago a now 49-year-old woman with Render-Osler-Weber disease showed unspecific symptoms of nausea, and general unwellness. Pulmonary manifestation of the disease was accompanied by pulmonary hypertension. METHODS Teleangiectasia of the tongue and pharynx as well as of the mucosa of

A surgical case of aortic stenosis with recurrent gastrointestinal bleeding: Heyde syndrome.

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BACKGROUND The combination of aortic stenosis, acquired coagulopathy, and anemia due to gastrointestinal (GI) bleeding is described as Heyde syndrome. METHODS We report a surgical case of a 77-year-old man who was admitted because of melena and exertional chest compression. GI endoscopy could not

Intrapericardial cystic hematoma in a dog treated by thoracoscopic subtotal pericardectomy.

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CASE DESCRIPTION A 2-year-old castrated male mixed-breed dog was evaluated because of a 1-week history of respiratory distress and abdominal distension. Thoracic radiography and echocardiography at that time revealed an enlarged cardiac silhouette and pericardial effusion; abdominal radiography and

Esophagoatrial fistula.

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The author describes a case of esophagoatrial fistula--an extremely rare condition. A 79-year-old-man had had epigastric pain for 4 weeks. Physical and roentgenographic examinations disclosed atrial fibrillation with a systolic murmur and an ulcer of the lower esophagus which, on histologic

Transcatheter closure of secundum-type atrial septal defect after failed surgical intervention.

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BACKGROUND Atrial septal defect (ASD) closure is routinely performed using transcatheter closure under echocardiographic guidance. METHODS A 24-year-old male was evaluated for a newly detected heart murmur. This was the first time a murmur or any other cardiac abnormalities were detected. He

Aortic Valve Replacement for the Management of Heyde Syndrome: A Case Report.

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Heyde syndrome describes the triad of aortic stenosis, acquired coagulopathy, and anemia due to bleeding from intestinal angiodysplasia. An 87-year-old man with iron deficiency anemia due to melena was admitted to our hospital. On examination, a systolic murmur was heard and echocardiography

Traumatic false aneurysms of the left ventricle after an attempt at video-thoracoscopic surgery.

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OBJECTIVES Video-thoracoscopic surgery (VTS) has been accepted as a safe and credible technique since 1990. Lung injury is one of the main perioperative complications. Few data are available about cardiac trauma and VTS-related false aneurysm of the left ventricular (LV) wall has not yet been

[Spontaneous regression of a posterior fossa dural arteriovenous malformation (author's transl)].

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A 29-year-old woman was admitted to our hospital because of dizziness, nausea and convulsive seizure. She complained of left sided tinnitus. Neurological examination revealed right homonymous hemianopsia, and systolic murmur on the left retroauricular area. Angiograms revealed a dural AVM in the

Valved apico-aortic conduit for relief of left ventricular hypertension caused by discrete subaortic stenosis in dogs.

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A double-outlet left ventricle (LV), with a valved conduit interposed between the LV apex and the aorta, was created in 7 dogs with subaortic stenosis. Of 8 dogs in which the implantation was attempted, 1 died following thoracotomy but before conduit implantation could be performed, 1 died from

Mitral valve prolapse with pulmonary haemosiderosis and severe anaemia: cause or association?

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A 12 years boy presented with the history of pallor for one month. Two days before hospitalisation he developed fever, cough, shortness of breath. He had past history of such episode. On examination, his heart rate was found to be 120/minute, respiratory rate 40/minute and moderate anaemia was

[Ventricular septal rupture after blunt chest trauma].

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METHODS Case 1: a 20-year-old previously healthy man sustained multiple nonvascular injuries without visible chest trauma in a car accident. Four days later a loud systolic murmur was heard over the heart. Case 2: a 21-year-old man similarly sustained in a car accident multiple injuries without

Transient mitral regurgitation due to mitral valve prolapse accompanied by systolic anterior motion of the mitral valve.

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A grade 4/6 systolic murmur, systolic anterior motion of the mitral valve (SAM), and severe mitral regurgitation (MR) documented by two-dimensional Doppler echocardiography developed suddenly on the structurally normal heart of a patient with idiopathic portal hypertension. The patient did not have
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