A 1-year-old female child presented with distention of abdomen, accompanied with occasional episodes of vomiting and abdominal pain for the past eight months with no history of constipation or fever. The child was vitally stable. On inspection upper abdomen was found distended and mild tenderness in epigas-trium on deep palpation. Laboratory investigations were within normal limits. The plain radiograph of ab-domen was unremarkable. Ultrasound scan showed a 6.9 cm x 7.5 cm sized cystic area with internal debris at porta hepatis, compressing the liver. CT scan showed a 5 cm x 7 cm sized cyst extending from porta hepatis to the duodenum (Fig. 1). The preopera-tive differentials were duodenal duplication and choledochal cyst. Figure 1: CT scan...
Concurrence of duodenal atresia and gastric duplication cyst is extremely rare entity. We report a 6...
A gastric duplication cyst (GDC) is a type of enteric duplication cyst. It can co‑exist with an ecto...
Duodenal duplication cysts are rare congenital abnormalities. We report the case of a 16 year old fe...
Duodenal duplication cyst consists 6% of alimentary tract duplications and the prevalence is estimat...
Duodenal duplication is a rare cause of acute pancreatitis in children. We report a case of acute pa...
A gastric duplication cyst (GDC) is a type of enteric duplication cyst. It can co-exist with an ecto...
A 61-year-old male presented to the hospital with a 5-day history of epigastric pain, vomiting and r...
A case of an ectopic gastric duplication cyst that appeared to arise from the pancreas in a 10-week-...
Introduction: Duplication of the alimentary tract is a relatively rare congenital anomaly. It can af...
Pyloroduodenal duplication is the rarest alimentary tract duplication known so far. A 1-year-old fem...
Gastric duplication cysts are rare variety of gastrointestinal duplications. Sometimes they may pres...
Introduction. Duodenal duplication cyst (DDC) is a rare congenital malformation that appears in the...
CONTEXT: Enteric duplication cysts are rare lesions of uncertain incidence and natural history. Pre...
Duodenal duplication cysts are rare congenital lesions. Their presentation is often non-specific and...
Context Enteric duplication cysts are rare lesions of uncertain incidence and natural history. Pre-o...
Concurrence of duodenal atresia and gastric duplication cyst is extremely rare entity. We report a 6...
A gastric duplication cyst (GDC) is a type of enteric duplication cyst. It can co‑exist with an ecto...
Duodenal duplication cysts are rare congenital abnormalities. We report the case of a 16 year old fe...
Duodenal duplication cyst consists 6% of alimentary tract duplications and the prevalence is estimat...
Duodenal duplication is a rare cause of acute pancreatitis in children. We report a case of acute pa...
A gastric duplication cyst (GDC) is a type of enteric duplication cyst. It can co-exist with an ecto...
A 61-year-old male presented to the hospital with a 5-day history of epigastric pain, vomiting and r...
A case of an ectopic gastric duplication cyst that appeared to arise from the pancreas in a 10-week-...
Introduction: Duplication of the alimentary tract is a relatively rare congenital anomaly. It can af...
Pyloroduodenal duplication is the rarest alimentary tract duplication known so far. A 1-year-old fem...
Gastric duplication cysts are rare variety of gastrointestinal duplications. Sometimes they may pres...
Introduction. Duodenal duplication cyst (DDC) is a rare congenital malformation that appears in the...
CONTEXT: Enteric duplication cysts are rare lesions of uncertain incidence and natural history. Pre...
Duodenal duplication cysts are rare congenital lesions. Their presentation is often non-specific and...
Context Enteric duplication cysts are rare lesions of uncertain incidence and natural history. Pre-o...
Concurrence of duodenal atresia and gastric duplication cyst is extremely rare entity. We report a 6...
A gastric duplication cyst (GDC) is a type of enteric duplication cyst. It can co‑exist with an ecto...
Duodenal duplication cysts are rare congenital abnormalities. We report the case of a 16 year old fe...