Title of article
Prenatal Diagnosis of Multiple rhabdomyma by Fetal echocardiography Method, clinical Outcome and Association with Tuberous Sclerosis complex
Author/Authors
Ramush Bejiqi، نويسنده , , Hana Bejiqi، نويسنده , , Ragip Retkoceri، نويسنده , , Mehmedali Azemi، نويسنده ,
Issue Information
فصلنامه با شماره پیاپی سال 2010
Pages
3
From page
236
To page
238
Abstract
In general cardiac tumors are very rare in infants and children, especially in neonatal period. In all ages (in children and fetuses) cardiac tumors are usually benign but may induce life threatening symptoms with nonspecific symptoms and often mimic other heart disease. predominate cardiac symptoms but they also can manifest sys¬temic and embolic symptoms too. The vide speed use of echocardiography and other non-invasive diagnostic methods in recent years has resulted in increase in detection of children and fetuses with cardiac tumors. Cardiac rhabdomyomas are the most com¬mon primary tumor of the heart in infants and children. The tumor is closely associated with tuberous sclerosis and occurs in more than 50 % of patients with this dis¬ease. We presented our experience of a case with fetal cardiac multiple rhabdomyoma diagnosed prenatally, the clinical outcome during the four year and association with tuberous sclerosis complex.
Keywords
cardiac tumor , prenatal echocardiography , Seizure , Tuberous sclerosis , rhabdomyoma
Journal title
Acta Informatica Medica
Serial Year
2010
Journal title
Acta Informatica Medica
Record number
685351
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