myxoma/إعياء

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[Cardiac myxoma in 13 patients].

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OBJECTIVE To gain insight into the occurrence, the manifestation and the treatment of cardiac myxoma. METHODS Retrospective. METHODS The departments of Cardiology and Cardiac Surgery of Middelheim General Hospital, Antwerp, Belgium. RESULTS Thirteen patients in the period 1985-1995 were subjected to

[Huge right atrial myxoma].

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Myxomas are account for approximately half of primary cardiac tumors, and 75% cases originate in left atrium. We report our experience of a right atrial myxoma. A 68-year-old woman was referred to us due to anorexia, general fatigue and facial edema. Echocardiogram, computed tomography (CT),

Hyperthyroidism and atrial myxoma--an intriguing cardio-endocrine association.

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A 65-year-old woman presented with dyspnea and bilateral leg edema for 1 week, worsening fatigue for 1 month, and a 7-lb weight loss over the last summer. She was clinically and biochemically hyperthyroid. Echocardiography revealed a left atrial myxoma measuring 6.2 x 3.3 cm protruding into the

Left atrial myxoma on FDG-PET/CT.

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A 56-year-old woman with rheumatoid factor-positive rheumatoid arthritis underwent FDG-PET/CT because of fatigue, fever, coughing, and weight loss for several months. FDG-PET/CT solely revealed a mildly hypermetabolic hypodense area in the left atrium. Subsequently, transthoracic echocardiography

Infected cardiac myxoma.

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A 66-year-old male presenting with low-grade fever and general fatigue was diagnosed as having infected myxoma of the left atrium. Blood cultures grew Streptococcus mitis. He underwent urgent resection and histological examination revealed tumor cells in a mucopolysaccharide matrix and bacterial

Atrial myxoma presenting as infective endocarditis.

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A 23-year-old Asian student presented to our service with a 1-month history of fever, weight loss of 10 kg, night sweats, fatigue and general malaise. He was previously well with no significant medical or family history. He had a low-grade pyrexia and cardiac auscultation revealed a diastolic murmur

Cardiac myxoma: sixteen-year experience in Central Chest Institute of Thailand.

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BACKGROUND Among the rare diseases of primary cardiac tumor myxoma is a leading pathology. A sixteen-year clinical experience and follow-up ofpatients with surgical removal of this particular mass is reported. METHODS Medical records of intracardiac tumor patients between April 1995 and June 2012

Cardiac myxoma showing extramedullary hematopoiesis in a patient with beta thalassemia.

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A 52-year-old woman presented with recurrent episodes of chest pain, shortness of breath, palpitations, and fatigue for three months. Her past medical history was significant for chronic anemia. Physical examination revealed a pansystolic murmur radiating to the left axilla. Her admission workup

[Left atrial myxoma with severe neovascularization: role of preoperative coronary angiography].

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Cardiac myxomas are highly vascular tumors and there is no consensus on the use of coronary angiography to assess their vascularity. A 64-year-old male patient presented with complaints of exertional dyspnea, fatigue, arthralgia, weight loss, intermittent high fever, and palpitation. He had an

[Clinical and echocardiographic features of cardiac myxomas in 64 patients].

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OBJECTIVE To summarize the clinical and echocardiographic features of cardiac myxomas. METHODS The medical records of patients with diagnosis of cardiac myxomas who hospitalized in our department from October 1985 to February 2011 were analyzed. RESULTS A total of 64 patients were enrolled [40

Giant left atrial myxoma in an elderly patient: natural history over a 7-year period.

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We present the case of a 71-year-old woman with a 7-year history of a giant left atrial myxoma. The myxoma was attached to the atrial septum and occupied almost the entire left atrial cavity. The patient was hospitalized 4 times because of dyspnea on exertion, palpitations, fatigue, general

Cardiac myxoma: clinical characteristics, surgical intervention, intra-operative challenges and outcome.

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OBJECTIVE The objectives of this retrospective study were to characterize the clinical presentation, diagnostic findings, surgical approaches, intra-operative challenges and complications following the surgical treatment of cardiac myxoma in two of the largest referral hospitals in

Primary cardiac tumors.

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From 1970 to 1986, 3 males and 6 females, ranging in age from 13 to 69 years (median 45 years), underwent heart surgery for a primary cardiac tumor. Six patients had a left atrial myxoma; a lipofibroma, a lymphosarcoma and a rhabdomyosarcoma were found each in 1 patient. The following complaints

Point-of-care Ultrasound to Complete Physical Exam and to Reach the Diagnosis in a Young Man With Syncope

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Background: Cardiac syncope can result from an atrial myxoma due to outflow obstruction. Myxoma is the most common primary cardiac tumor that may cause sudden death and the nonspecific symptoms may make early diagnosis difficult. Case

Unusual cause of infective endocarditis in an elderly patient with a rare condition.
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A 77-year-old woman presented to the emergency department with a 1-week history of anorexia, fatigue, general malaise and a 3-day history of fever. Clinical examination revealed livedo reticularis across the anterior aspect of her knees and a pansystolic murmur. Laboratory evaluation found

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