Jejunal web masquerading as intestinal malrotation in a neonate with bilious vomiting: A case report
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چکیده
منابع مشابه
Adult Intestinal Malrotation: A Case Report
Midgut malrotation is an anomaly of intestinal rotation which occurs during fetal development and usually presents in the neonatal period. It is rare for malrotation to present in adulthood. We present a case of malrotation in an adult female patient who presented with cramping generalized right abdominal pain and vomiting of one day duration. A computed tomography abdominal scan and upper gast...
متن کاملIntestinal malrotation in an adult: case report.
Intestinal malrotation is a developmental anomaly of the midgut in which the normal fetal rotation of intestines around the superior mesenteric artery and their fixation in the peritoneal cavity fail. Rotational anomalies of the midgut are rare in adults. Operative intervention is required generally when they are symptomatic. While difficult to diagnose, prompt recognition and surgical treatmen...
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The testicular torsion which is typically seen in prepuberty is very rare in the early neonatal period; prenatal diagnosis is difficult. Herein, we report a five day-old male neonate with swelling and erythema of the right scrotum. Following Doppler ultrasound suggestive of testicular torsion, surgical exploration was undertaken. There was gangrene of the right testis with discoloration and ne...
متن کاملJejunal perforation as an unusual presentation of total colonic aganglionosis in a neonate: A case report
INTRODUCTION Neonatal intestinal perforation usually occurs at distal small bowel secondary to distal bowel obstruction. The aim of this report is to describe an unusual case of total colonic aganglionosis with an initial presentation of proximal jejunal perforation. PRESENTATION OF CASE A male newborn presented with jejunal perforation on the fifth day of life and was treated by laparoscopic...
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Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence of 1 case per 1000,000 individuals. It is a form of predominantly autosomal dominant inheritance and is associated with a mutation in runt related transcription factor-2 gene mapped on chromosome 6p21. This disease primarily affects the bones formed by intramembranous ossification and is characte...
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ژورنال
عنوان ژورنال: Journal of Pediatric Surgery Case Reports
سال: 2015
ISSN: 2213-5766
DOI: 10.1016/j.epsc.2015.05.010