A CASE REPORT: PRENATAL DIAGNOSIS OF FETAL CARDIAC RHABDOMYOMA
نویسندگان
چکیده
Fetal cardiac rhabdomyoma is a rare disease, and most of the cases are detected incidentally during antenatal ultrasound. This case discovered ultrasonography at 29 weeks gestation. Multiple hyperechoic round shape masses were seen in cardiac. After birth, baby had been under paediatric cardiologist follow-up with regular echocardiography. Management was mainly conservative time being as there no sign obstruction.
منابع مشابه
Case Report Cardiac Rhabdomyoma — A Case Report
Cardiac tumors are rare in neonates, most are rhabdomyomas. Because of large size, they may cause homodynamic instability and even death in neonatal period. In 50% cases, rhabdomyoma is associated with tuberous sclerosis [1]. About 100 cases have been reported in literature [1, 3]. We are reporting a case of term neonate, with antenatally diagnosed cardiac masses, who expired at 36 h of life an...
متن کاملPrenatal sonographic diagnosis of fetal cardiac rhabdomyoma: a case report* Diagnóstico pré-natal de rabdomioma cardíaco fetal pela ultrassonografia: relato de caso
Os tumores cardíacos constituem condição rara, com incidência entre 0,17 e 28/10.000 na população geral. Os rabdomiomas são os tumores mais frequentes no período pré-natal. Este trabalho tem como objetivo relatar o caso de um feto com 31 semanas de gestação que apresentava tumoração intracardíaca de grandes dimensões, com graves repercussões clínicas. Unitermos: Diagnóstico pré-natal; Ultrasson...
متن کاملFetal Rhabdomyoma of the upper Extremity in a 31- Year Old Patient: a Case Report
Fetal rhabdomyomas (RM) are extremely rare benign mesenchymal tumours that occur primarily in the head and neck.This tumour exhibits immature skeletal muscle differentiation. The patients’ median age is four years and surgical resectionis the recommended treatment.Fetal RM of limbs are rare and not well described in the literature and if, predominantly in form of case reports. We reportthe seco...
متن کاملPrenatal Diagnosis of Fetal Peters' Plus Syndrome: A Case Report
Peters' plus syndrome is a rare but clinically recognizable autosomal recessive ocular genetic syndrome. Diagnosis during the fetal life is challenging due to the presence of nonspecific findings such as ventriculomegaly in the growth-retarded fetuses. We report the first case of fetal Peters' plus syndrome from India, where fetal ultrasound and the family history were helpful in providing a cl...
متن کاملPrenatal Diagnosis of Fetal Seizure: A Case Report
A 35-yr-old woman carrying a 17-week-old fetus presented with right hydronephrosis and a single umbilical artery. Karyotyping was normal and targeted ultrasonography showed an otherwise normal fetus. After 28 weeks of gestation, the mother felt rapid, repetitive fetal movement and an ultrasound at 30 weeks of gestation revealed tonic clonic movements of the fetal trunk and extremities. At 36 we...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Malaysian Journal of Medical Research
سال: 2021
ISSN: ['2550-1607']
DOI: https://doi.org/10.31674/mjmr.2021.v05i03.001