منابع مشابه
Neonatal Duodenal Duplication Cyst
A 2800 gram baby boy was born with a prenatal diagnosis of a choledochal cyst; he was admitted to NICU for further evaluation. Clinically he was jaundiced with a palpable abdominal mass in the right hypochondrium. Choledochal and duplication cysts were differential diagnoses. Ultra-sonography by an experienced sonographer or a CT scan is usually sufficient for diagnosis. Communicating duplicati...
متن کاملDuodenal duplication cyst.
Tang SJ et al. Duodenal Duplication Cyst · Endoscopy 2002; 34: 1028–1029 A 42-year-old man presented with a 2year history of vague epigastric discomfort, intermittent nausea and vomiting. The patient denied weight loss. Results of the laboratory studies were normal except for a persistently elevated lipase level within a range of 150–300U/l (normal range, 17–55). The serum albumin level was 3.8...
متن کاملA Case of Duodenal Duplication Cyst Manifested by Duodenal Polyp
Duodenal duplication cyst is a rare anomaly, totaling only 4% to 12% of gastrointestinal duplications, and is usually encountered during infancy or in early childhood. Most are commonly located posterior to the first or second portion of the duodenum. Presenting signs and symptoms include vomiting, decreased oral intake, periumbilical tenderness, abdominal distention, obstructive jaundice, acut...
متن کاملEndoscopic treatment of a duodenal duplication cyst.
A young lady presented to the emergency department with pain in the abdomen for 1 day. She had a history of similar pain in the past. Her clinical examination was unremarkable, except for mild abdominal tenderness. Further investigations suggested diagnoses of acute pancreatitis and a duodenal cyst. Magnetic resonance cholangiopancreatography (MRCP) revealed a cystic lesion in the duodenum in c...
متن کاملGallbladder Duplication Associated with Duodenal Atresia
Gallbladder duplication is an extremely rare anomaly. Association of gall bladder agenesis with duodenal atresia and biliary atresia has been described. However, association of gall bladder duplication with duodenal atresia hasn't been described so far; we report a case in view of its rarity.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Annals of Surgery
سال: 1965
ISSN: 0003-4932
DOI: 10.1097/00000658-196511000-00016