Spontaneous regression of cardiac rhabdomyoma with tuberous sclerosis
Joint Authors
Qurayshi, Ubaydah
Abd al-Jalil, Rawan
Source
Issue
Vol. 41, Issue 2 (30 Jun. 2019), pp.121-123, 3 p.
Publisher
King Hamad University Hospital
Publication Date
2019-06-30
Country of Publication
Bahrain
No. of Pages
3
Main Subjects
Abstract EN
Fetal cardiac rhabdomyoma is the most common cardiac tumor diagnosed antenatally.
It has a strong association with tuberous sclerosis.
A case of cardiac rhabdomyoma was diagnosed at 22 weeks of gestation through an anomaly scan.
The scan revealed multiple masses related to the ventricular myocardium with no vessel obstruction.
The diagnosis of cardiac rhabdomyoma with tuberous sclerosis was confirmed at birth.
Repeated echocardiography at three months of life showed slight regression of the tumor size and no deterioration of the cardiovascular status.
The most common cardiac tumor in children is rhabdomyoma, which may disappear spontaneously without treatment.
They could be asymptomatic or present as heart failure and respiratory distress which requires surgical intervention.
All these children, even those who are asymptomatic, need regular serial follow-ups including echocardiographs.
American Psychological Association (APA)
Abd al-Jalil, Rawan& Qurayshi, Ubaydah. 2019. Spontaneous regression of cardiac rhabdomyoma with tuberous sclerosis. Bahrain Medical Bulletin،Vol. 41, no. 2, pp.121-123.
https://search.emarefa.net/detail/BIM-889271
Modern Language Association (MLA)
Abd al-Jalil, Rawan& Qurayshi, Ubaydah. Spontaneous regression of cardiac rhabdomyoma with tuberous sclerosis. Bahrain Medical Bulletin Vol. 41, no. 2 (Jun. 2019), pp.121-123.
https://search.emarefa.net/detail/BIM-889271
American Medical Association (AMA)
Abd al-Jalil, Rawan& Qurayshi, Ubaydah. Spontaneous regression of cardiac rhabdomyoma with tuberous sclerosis. Bahrain Medical Bulletin. 2019. Vol. 41, no. 2, pp.121-123.
https://search.emarefa.net/detail/BIM-889271
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 123
Record ID
BIM-889271