A case with annular pancreas and accompanying ectopic pancreas
نویسندگان
چکیده
منابع مشابه
Introducing a Specimen of Annular Pancreas (with late-onset Symptoms)
Annular pancreas is a relatively rare congenital diseasecaused by an embryologica1and anatomical disturbance in pancreas It may have no sympforns throughout the life and so occasionally discovered during an unrelevant surgery or autopsy but in most of the cases it shows itself as a duodenal obstruction during the infancy and childhood.Very rarely symptoms of the disease my be observed in adul...
متن کاملAn Unusual Presentation of Annular Pancreas: A Case Report
Abstract Annular pancreas (AP) is a rare congenital malformation resulting from failure of pancreas ventral anlage rotation with the duodenum. This leads to a ring of pancreatic tissue that envelops the duodenum. Clinical manifestations of AP most commonly develop in infancy or early childhood but can present at any age. The diagnosis of AP, usually suggested by an upper GI series or abdominal ...
متن کاملA strange case of double annular pancreas.
CONTEXT The pancreas is a soft lobulated gland situated transversely across the upper part of the posterior abdominal wall. Its parts include the head, neck, body and tail. Annular pancreas is a rare condition where the head of the pancreas surrounds the second part of the duodenum like a ring. CASE REPORT We observed a rare type of double annular pancreas where the uncinate process encircled...
متن کاملAnnular Pancreas
Introduction Annular pancreas (from the Latin annularis, meaning ring-shaped) is a rare congenital disorder of the pancreas first recognised by Tiedeman in 1818. This abnormality, although at times clinically silent, may be the cause of a broad spectrum of disease. Complications range from neonatal intestinal obstruction to more complex pathologies in the adult. In cases of neonatal obstruction...
متن کاملSmith-Lemli-Opitz Syndrome: A Case with Annular Pancreas
Smith-Lemli-Opitz syndrome is an autosomal recessive disease of cholesterol metabolism. It is a multiple malformation syndrome with typical dysmorphic features such as bitemporal narrowing, ptosis, epicanthus, microcephaly, micrognathia, and cardiovascular, skeletal, urogenital, and gastrointestinal anomalies. This report presents a typical case of Smith-Lemli-Opitz syndrome with annular pancre...
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ژورنال
عنوان ژورنال: Laparoscopic Endoscopic Surgical Science
سال: 2021
ISSN: 2587-0610
DOI: 10.14744/less.2021.24471