Duodenal atresia and sudden fetal death. Running head: Prenatal diagnosis of fetal duodenal atresia and risk of fetal adverse outcome

نویسندگان

  • Giuseppe Trojano
  • Lorella Battini
  • Pietro Bottone
  • Veronica Tosi
  • Chiara Nanini
  • Arianna Carmignani
  • Maria Giovanna Salerno
چکیده

Duodenal atresia occurs in approximately 1:10.000 live births. The outcome of congenital duodenal obstructions, in terms of mortality rate, has improved over the last decades, mainly attributable to the improvement in the quality of prenatal diagnosis and neonatal intensive care. Nevertheless, several cases of sudden intrauterine fetal death (IUFD) in fetuses with duodenal obstruction have been described in the Literature. We report a case of a fetus with duodenal atresia and sudden IUFD at 32 weeks’ gestation and the review of literature. We speculate that the fetal demise was due to a vaso-vagal reaction initiated by esophageal dysmotility. This report is intended to describe the features of duodenal obstruction on prenatal ultrasonography and alert the obsterician to the possible association with sudden IUFD.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Twin pregnancy complicated by esophageal atresia, duodenal atresia, gastric perforation, and hypoplastic left heart structures in one twin: a case report and review of the literature

BACKGROUND The antenatal diagnosis of a combined esophageal atresia without tracheoesophageal fistula and duodenal atresia with or without gastric perforation is a rare occurrence. These diagnoses are difficult and can be suspected on ultrasound by nonspecific findings including a small stomach and polyhydramnios. Fetal magnetic resonance imaging adds significant anatomical detail and can aid i...

متن کامل

Intestinal atresia, encephalocele, and cardiac malformations in infants with 47,XXX: Expansion of the phenotypic spectrum and a review of the literature.

Identification of the 47,XXX karyotype often occurs adventitiously during prenatal fetal karyotyping in cases of advanced maternal age. Although most females with 47,XXX appear healthy at birth, various types of congenital malformations have been reported, of which urinary tract anomalies are the most frequent. We report on 2 newborns with 47,XXX and congenital cardiac defects, one of whom had ...

متن کامل

Association of Fetal and Parental Chromosomal Abnormalities with Congenital Anomalies

Background & Aims: Chromosome abnormalities are a major cause of miscarriage and neonatal mortality. The present study aimed to determine the association of fetal and parents chromosomal abnormalities with congenital anomalies. Methods: A cross-sectional study was performed in a tertiary referral center (Afzalipour Hospital) over 16 months period (2011-2012). The study groups consisted of 77 fe...

متن کامل

Perinatal outcome after prenatal diagnosis of single-ventricle cardiac defects.

OBJECTIVES To investigate the perinatal outcome of cases with a prenatal diagnosis of single-ventricle cardiac defects, single ventricle being defined as a dominant right ventricle (RV) or left ventricle (LV), in which biventricular circulation was not possible. METHODS We reviewed patients with a prenatal diagnosis of single-ventricle cardiac defects, made at one institution between 1995 and...

متن کامل

A Retrospective Analysis of Duodenal and Jejunointestinal Atresia-Five-Year Experience from a Tertiary Care Paediatric Surgery Center in Western India.

Background: Intestinal atresia is a life-threatening problem requiring early active intervention. The aim of the study was to compare management outcomes between Duodenal-Atresia (DA) and Jejunoileal-Atresias (JIA). The secondary objective was to analyse tapering enteroplasty versus end-to-end anastomosis in JIA. Materials and Methods: Retrospective descriptive analysis of patients operated be...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2016