نتایج جستجو برای: myxomas

تعداد نتایج: 591  

Journal: :British Journal of Ophthalmology 1991

2012
Vinícius JS Nina Nathalia AC Silva Shirlyne FD Gaspar Thaísa L Rapôso Eduardo C Ferreira Rachel VAH Nina Joyce S Lages Fernando ACC Silva Natalino Salgado Filho

INTRODUCTION Primary intracardiac tumors are rare and approximately 50% are myxomas. The majority of myxomas are located in the left atrium and have variable clinical presentation. We report a case of a large myxoma in the right atrium, which is an uncommon location for this type of tumor. CASE PRESENTATION A 45-year-old Caucasian woman with a history of palpitation had dyspnea on great exert...

2005
NIKOLAUS SCHAD

YXOMA is an infrequent but important LYE intracardiac lesion which occurs most often in the left atrium. Although it has been suggested that atrial myxomas merely represent degenerated thrombi, evidence strongly favors a neoplastic origin.1 Since the first successful removal of an intracardiac myxoma in 1955,2 numerous reports dealing with surgical resection of these tumors have appeared in the...

2014
Panagiota Kourkoveli Dimitrios Tsiapras Evaggelia Grisbolaki Olga Karapanagiotou Stamatina Kampanarou Stamatis Kyrzopoulos Loukas Kaklamanis Mazen Khoury Vassilis Voudris

INTRODUCTION Myxomas are the most common benign tumors of the heart. They vary widely in size, and little is known about their growth rate. The present case report is, we believe the first in bibliography that provides images of an apical left ventricular myxoma from transthoracic echocardiography and computed tomography scans taken a year apart. CASE PRESENTATION We present the rare case of ...

2005
Laurie E. Knepper Harold P. Adams

We present the results of a 12-year retrospective analysis of 11 patients, eight women and three men, aged 16-76 years, with pathologically documented atrial myxomas. Nine of the 11 patients were found to have a left atrial myxoma; right atrial myxomas were identified in two. Five of the 11 patients (45%) had abnormalities on neurologic examination, and five of five had computed tomographic evi...

Journal: :Texas Heart Institute journal 1986
L W Pechacek F Gonzalez-Camid R J Hall E Garcia C M de Castro R D Leachman G Montiel-Amoroso

We analyzed the echocardiograms of 28 patients with a left atrial myxoma and two with a right atrial myxoma. Our purpose was to evaluate the value of echocardiography for the diagnosis of these cardiac masses. Only 59% of the m-mode echocardiograms in patients with a left atrial myxoma showed the characteristic findings of multiple diastolic echoes within the mitral orifice as well as abnormal ...

Journal: :Stroke 1988
L E Knepper J Biller H P Adams A Bruno

We present the results of a 12-year retrospective analysis of 11 patients, eight women and three men, aged 16-76 years, with pathologically documented atrial myxomas. Nine of the 11 patients were found to have a left atrial myxoma; right atrial myxomas were identified in two. Five of the 11 patients (45%) had abnormalities on neurologic examination, and five of five had computed tomographic evi...

Journal: :The British journal of ophthalmology 1991
H E Grossniklaus I W McLean J J Gillespie

A 21-year-old man with a history of an excised soft tissue mass of the groin and spotty cutaneous pigmentation underwent excision of nodules of the right lower and left upper eyelids. The patient subsequently had a cutaneous mass of the left ear removed. All excised lesions were classified as myxomas. A diagnosis of multiple myxoma, spotty pigmentation, and endocrine overactivity (Carney's) com...

Journal: :Revista espanola de cardiologia 2008
Jesus Vargas-Barrón Gilberto Vargas-Alarcón Francisco-Javier Roldán Clara Vázquez-Antona Zuilma Vásquez Ortiz Julio Erdmenger-Orellana Angel Romero-Cárdenas

The study involved 63 patients with an echocardiographic, surgical and histopathologic diagnosis of cardiac myxoma who were seen over a period of 20 years. Tumor recurrence or relapse was documented in five of these patients (7.9%), 3 of whom had a confirmed diagnosis of Carney complex, while one other patient had a probable diagnosis. Genetic studies demonstrated abnormalities in the PRKAR1A g...

Journal: :Interactive Cardiovascular and Thoracic Surgery 2003

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