Prenatal diagnosis of a complex fetal cardiac malformation associated with asplenia.
نویسندگان
چکیده
A case of a complex fetal heart malformation with left isomerism, a "right sided" double outlet ventricle, and aortic isthmus stenosis combined with asplenia was diagnosed by ultrasonography at 26 weeks' gestation. The pregnancy was terminated at the request of the parents in the 27th week of gestation. Because the prognosis for a fetus with cardiosplenic syndromes depends mainly on the severity of the cardiac abnormality cases of visceral heterotaxy should be classified according to the predominant feature, the heart malformation.
منابع مشابه
Prenatal diagnosis and postnatal findings of cloacal malformation: a case report
Introduction: Cloacal malformation is an extremely rare fetal pathological condition but an important anomaly that presents as a variety of defects. It predominantly affects females, with prevalence of 1 in 50,000 births. Prenatal ultrasonography usually showed oligohydramnios and the fetus having a large cystic mass in the lower abdomen with a single septum, bilateral hydronephrosis, ambig...
متن کاملگزارش یک مورد نوزاد با علائم شبیه به سندرم هیدانتوئین ناشی از مصرف قرص فنوباربیتال در زمان حاملگی INFANT WITH HYDANTOIN SYNDROME DUE TO PRENATAL PHENOBARBITAL EXPOSURE
I ABSTRACT Phenobarbital is a drug of barbiturates class that it’s Anticonvulsant and sedative effects has been caused it’s widely. Usage in nervous system diseases espicially epilepsy. The epileptic pregnant women who taking this dr...
متن کاملThe Ultrasonic Microsurgical Anatomical Comparative Study of the CHD Fetuses and Their Clinical Significance
The aim of our study was to increase the detection rate of fetal cardiac malformations for congenital heart disease (CHD). The ultrasonic and microanatomical methods were combined to study the CHD cases firstly, which could provide the microsurgical anatomical basis to the prenatal ultrasonic diagnosis which was used in suspected CHD and help the sonographer to improve the quality of fetal card...
متن کاملگزارش یک مورد نادر رابدومیوما در قلب جنین: گزارش موردی
Background: The primary manifestation of cardiac tumors in embryonic period is a very rare condition. Cardiac rhabdomyomas most frequently arise in the ventricular myocardium, they may also occur in the atria and the epicardial surface. In spite of its benign nature, the critical location of the tumor inside the heart can lead to lethal arrhythmias and chamber obstruction. Multiple rhabdomyomas...
متن کاملComplementary findings on 18F-FDG PET/CT and 18F-NaF PET/CT in a patient with Erdheim-Chester disease
Radiol Bras. 2017 Mai/Jun;50(3):199–208 202 congenital anomalies, such as congenital heart disease and gastrointestinal anomalies. The prenatal diagnosis is based on identification of this pattern of malformation in imaging studies. Sirenomelia is considered a primary developmental field defect affecting multiple midline primordia. In the case reported here, MRI allowed us to make the diagnosis...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- British heart journal
دوره 65 5 شماره
صفحات -
تاریخ انتشار 1991