Duodenal duplication cysts are rare congenital lesions usually diagnosed in infancy, although they may present in adulthood. Prenatal diagnosis is difficult, and postnatal diagnosis relies on ultrasonography, barium swallow, contrast-enhanced computerized tomography, magnetic resonance imaging (MRI), and magnetic resonance cholangiopancreatography. A female newborn was diagnosed with an abdominal cyst (size around 6 x 5 x 4 cm) at gestational age (GA) 24 weeks, by regular prenatal examination. After her birth at GA 37 weeks, we performed abdominal ultrasonography and MRI, but there was no definite diagnosis. The usual management of an abdominal cyst involves resection by laparotomy (requiring a large incision ) or laparoscopy (requiring sev...
AbstractINTRODUCTIONDuodenal duplication is a rare congenital malformation. Although more frequent i...
Duodenal duplication cysts are rare congenital abnormalities. We report the case of a 16 year old fe...
Duodenal duplication cysts are rare congenital anomalies, found commonly in infants and children. In...
Duodenal duplication cysts are rare congenital lesions. Their presentation is often non-specific and...
Duodenal duplication cysts are rare congenital lesions. Their presentation is often non-specific and...
Abstract Background Duodenal duplication cyst is an uncommon foregut...
Background: Duodenal duplication cysts (DDCs) are rare congenital anomalies typically manifesting du...
AbstractINTRODUCTIONDuodenal duplication is a rare congenital malformation. Although more frequent i...
BACKGROUND& nbsp;Duodenal duplications are rare congenital anomalies of the gastrointestinal tract. ...
Introduction: Duodenal duplication is a rare congenital malformation. Although more frequent in chil...
A 1-year-old female child presented with distention of abdomen, accompanied with occasional episodes...
Bilious vomiting is a relevant sign in neonates that requires immediate evaluation and diagnosis. A ...
PURPOSE:The aim of this study was to evaluate delayed elective resection of antenatally detected ent...
Background: Duodenal duplication cysts are rare congenital anomalies. Symptomatic cases have classic...
Abstract Background Gastric duplication cysts are rare congenital alimentary tract anomalies and mos...
AbstractINTRODUCTIONDuodenal duplication is a rare congenital malformation. Although more frequent i...
Duodenal duplication cysts are rare congenital abnormalities. We report the case of a 16 year old fe...
Duodenal duplication cysts are rare congenital anomalies, found commonly in infants and children. In...
Duodenal duplication cysts are rare congenital lesions. Their presentation is often non-specific and...
Duodenal duplication cysts are rare congenital lesions. Their presentation is often non-specific and...
Abstract Background Duodenal duplication cyst is an uncommon foregut...
Background: Duodenal duplication cysts (DDCs) are rare congenital anomalies typically manifesting du...
AbstractINTRODUCTIONDuodenal duplication is a rare congenital malformation. Although more frequent i...
BACKGROUND& nbsp;Duodenal duplications are rare congenital anomalies of the gastrointestinal tract. ...
Introduction: Duodenal duplication is a rare congenital malformation. Although more frequent in chil...
A 1-year-old female child presented with distention of abdomen, accompanied with occasional episodes...
Bilious vomiting is a relevant sign in neonates that requires immediate evaluation and diagnosis. A ...
PURPOSE:The aim of this study was to evaluate delayed elective resection of antenatally detected ent...
Background: Duodenal duplication cysts are rare congenital anomalies. Symptomatic cases have classic...
Abstract Background Gastric duplication cysts are rare congenital alimentary tract anomalies and mos...
AbstractINTRODUCTIONDuodenal duplication is a rare congenital malformation. Although more frequent i...
Duodenal duplication cysts are rare congenital abnormalities. We report the case of a 16 year old fe...
Duodenal duplication cysts are rare congenital anomalies, found commonly in infants and children. In...