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heart neoplasms/mæði

Krækjan er vistuð á klemmuspjaldið
GreinarKlínískar rannsóknirEinkaleyfi
Bls 1 frá 19 niðurstöður

Massive right atrial myxoma with dyspnea at rest in an elderly patient: a case report.

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BACKGROUND Primary heart tumors are extremely rare and myxoma is the most common type of these tumors. Although intra-atrial presentation is a predilection place, right atrial localization is atypical. The symptom triad is characteristic in the clinical presentation of the tumor: embolic

Heart neoplasms in children: retrospective analysis.

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BACKGROUND The advancement of noninvasive imaging methods has resulted in the increase in diagnosis of heart neoplasms. However, the literature has few studies involving primary cardiac neoplasms in children. OBJECTIVE To retrospectively review cases of primary heart neoplasms in children,

[Primary atrial heart tumors--a review of 21 cases].

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Between 1978 and 1986, atrial heart tumors were found in 21 of our patients, all of them subsequently underwent surgery. Pathological-histological examination in 20 patients confirmed the diagnosis of a myxoma; the one remaining case was a female patient with primary cardiogenic osteosarcoma. Of the

Heart tumors in Puerto Rico de novo atrial fibrillation as clinical presentation in a subgroup of patients.

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OBJECTIVE Primary cardiac tumors are rare neoplasms in humans, of which the most common is the atrial Myxoma. The objective of this study was to find the incidence of these tumors at the Heart Center of Puerto Rico and the Caribbean. METHODS This study was approved by the Institutional Review Board

Massive right atrial myxoma presenting as syncope and exertional dyspnea: case report.

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Primary heart neoplasms are rare occurring with an estimated incidence of 0.0017-0.19%. Myxoma is the most prevalent primary heart tumor. The right atrium is an unusual localization, occurring only in 15-20% of myxoma cases. We report a rare case of a massive right atrial myxoma causing tricuspid

[Clinical analysis for 232 cases of primary heart neoplasms].

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OBJECTIVE To summarize the clinical characterizations and outcome of surgical treatment of primary heart neoplasms. METHODS The clinical data of cardiac neoplasms were analyzed retrospectively in 232 patients. There were 14 malignant tumors (6.0%) and 218 benign tumors (94.0%), of which 200 were

[Clinical, anatomical-pathological and therapeutic correlates of benign intracavitary heart tumors].

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Benign intracavitary cardiac tumors lead to "malignant" complications, so early diagnosis and adequate treatment are of vital importance. Our investigation summarizes a 10-year experience after surgical treatment of 29 patients suffering from benign intracavitary cardiac tumors. The postoperative

Case report of death from falling: Did heart tumor cause syncope?

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A healthy man in his 30s was working on the balustrade of stairs on the second floor. He suddenly fell downstairs without saying anything. On emergency hospitalization, chest echogram showed left hemothorax. Cardiac echogram showed a floating mass from the mitral valve in the left ventricle and

Cardiac Involvement by Burkitt Lymphoma in a 49-Year-Old Man

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Malignant metastases are among the most common cardiac masses. We report a rare case of cardiac involvement by Burkitt lymphoma in a 49-year-old man who presented with a 2-month history of dyspnea and palpitations. A transthoracic echocardiogram revealed 2 intracardiac masses in the right atrium

Huge right ventricular mass lesion associated with genital malignant tumor: a case report.

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BACKGROUND Primary heart tumors are rare, whereas metastatic heart tumors occur more frequently. METHODS We report a case of a 75-year-old Japanese woman who had metastatic heart tumors of the right ventricle. Although she initially received antibiotic therapy following a diagnosis of pneumonia and

Symptomatic metastatic right atrial lymphoma in a patient with AIDS presenting with pulmonary embolization.

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Tumors involving the heart are rare, and the majority of them are benign. Secondary lymphoma with localization to the heart is the third most common malignant heart tumor and is more common, by far, than primary cardiac lymphomas. In patients with human immunodeficiency virus, the risk of

Clinical manifestation and surgical treatment analysis of five cases with biatrial myxoma.

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BACKGROUND Cardiac myxomas (CMs) are a major primary heart tumor which often causes unexpected symptoms or sudden death. Among CMs, biatrial myxomas are even rare. This study was designed to investigate the clinical characteristics and surgical treatment of 5 cases with biatrial myxoma, to summarize

[Papillary cardiac fibroelastoma. An unusual presentation].

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BACKGROUND Papillary fibroelastoma is a rare benign tumor characterized morphologically since first being described in 1976. Nevertheless, this tumor can be presented with a variety of clinical manifestations, making diagnosis challenging for the physician. There are no gender or age preferences but

Voluminous Intrapericardial Lipoma Mimicking Pericardial Effusion

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Lipomas are rare primary heart tumors and may involve the endocardium, myocardium, or pericardium. Signs and symptoms depend on the tumor location and size. The intrapericardial lipoma we report has massive dimensions and mimics a pericardial effusion. A 38-year-old male complained of dyspnea and

Right ventricular myxoma in a 12-year-old child: a case report.

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Cardiac myxoma especially of the right ventricle, is rare in children. A 12-year-old boy with right ventricle myxoma is reported. His heart murmur was found incidentally when he visited the Outpatient Department (OPD) because of upper respiratory infection symptoms. There was no exertional dyspnea,
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