Complete agenesis of dorsal pancreas

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A Rare Case of Complete Agenesis of Dorsal Pancreas

Agenesis of dorsal pancreas (ADP) is an extremely rare congenital anomaly that results from defective development of pancreas. Most ADP patients are asymptomatic; if symptomatic, they present with epigastric pain. About half of affected individuals develop diabetes mellitus (DM), resulting from reduced islet cell mass secondary to the absence of endocrine structures. Being very rare, it is gene...

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Sonographic features of agenesis of dorsal pancreas

Agenesis of dorsal pancreas is an extremely rare congenital anomaly that occurs due to failure of the dorsal pancreatic bud to form the body and tail of the pancreas. We report the sonographic appearance of this condition in six cases.

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CT diagnosis of dorsal pancreas agenesis.

We report a case of agenesis of dorsal pancreas diagnosed by CT. This anomaly can easily be confused with pancreas divisum on endoscopic retrograde cholangiopancreatography alone.

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Complete agenesis of the dorsal pancreas: Case report with imaging findings and review of the literature.

http://dx.doi.org/10.4314/mmj.v27i2.9 Introduction A 35-year-old male presented with a three-day history of epigastric pain and vomiting. Six months prior to presentation, the patient was diagnosed with type 2 diabetes mellitus and was on an insulin therapy regimen. He had no relevant history of familial illness. He reported 20 years of chronic, heavy alcohol consumption. Physical examination r...

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Complete dorsal pancreatic agenesis and unilateral renal agenesis

Dorsal pancreatic agenesis is a very rare congenital anomaly. Unilateral renal agenesis, on the other hand, is a relatively common congenital anomaly, although its etiology is not fully understood. Renal and pancreatic embryologic development appears to be nonrelated. We report a case of a 34-year-old man who was referred to our hospital for evaluation of cholestasis and microalbuminuria. Ultra...

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ژورنال

عنوان ژورنال: Oncology, Gastroenterology and Hepatology Reports

سال: 2014

ISSN: 2348-3113

DOI: 10.4103/2348-3113.126641