Spontaneous regression of cardiac rhabdomyoma with tuberous sclerosis

المؤلفون المشاركون

Qurayshi, Ubaydah
Abd al-Jalil, Rawan

المصدر

Bahrain Medical Bulletin

العدد

المجلد 41، العدد 2 (30 يونيو/حزيران 2019)، ص ص. 121-123، 3ص.

الناشر

مستشفى الملك حمد الجامعي

تاريخ النشر

2019-06-30

دولة النشر

البحرين

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الملخص 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.

نمط استشهاد جمعية علماء النفس الأمريكية (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

نمط استشهاد الجمعية الأمريكية للغات الحديثة (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

نمط استشهاد الجمعية الطبية الأمريكية (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

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 123

رقم السجل

BIM-889271