2002, Number 6
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Cir Cir 2002; 70 (6)
Rhabdomyoma of the right atrium. A case report
García-Aranda A, García-Torres CD, Sánchez-Medina F
Language: Spanish
References: 20
Page: 455-458
PDF size: 68.58 Kb.
ABSTRACT
Von Recklinghausen described de first rhabdomyoma in 1862. These tumors are considered benign due to their morphologic features; however, they can be the source of many clinical findings, rendering them a diagnostic challenge for the physician. Rhabdomyoma is the most frequent cardiac neoplasm of childhood. The majority of children with cardiac rhabdomyoma also have tuberous sclerosis, characterized by mental retardation, epilepsy, and adenoma sebaceum; it is uncommon in healthy adult population. Until the 1950s, cardiac tumors were merely a curiosity. Diagnosis was academic and of autopsy-related. More recently, development of cardiopulmonary bypass and invasive and non-invasive diagnostic technology has contributed greatly to the process of preoperative diagnosis. We describe here a previously healthy women who presented with heart and renal failure resulting from right atrium cardiac rhabdomyoma.
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