1985
DOI: 10.1016/0016-5085(85)90193-3
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Pancreas divisum: Congenital anatomic variant or anomaly?

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Cited by 229 publications
(27 citation statements)
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“…[1][2][3][4][5] The anomaly results from a failure of fusion of the dorsal and ventral pancreatic buds during fetal development. Several studies have shown an extremely high incidence of this anomaly, reaching 25%-50%, in patients with idiopathic pancreatitis.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5] The anomaly results from a failure of fusion of the dorsal and ventral pancreatic buds during fetal development. Several studies have shown an extremely high incidence of this anomaly, reaching 25%-50%, in patients with idiopathic pancreatitis.…”
Section: Introductionmentioning
confidence: 99%
“…While the malformation is present in 5-15% of patients in autopsy series, only a few such patients develop recurrent pancreatitis [2,3]. Indeed, a recent large study failed to demonstrate a relationship between this anatomic variant and pancreatic disease [4]. Still, patients with pancreas divisum remain susceptible to other established causes of pancreatitis, and the influence of the congenital anomaly on the course of these illnesses is…”
mentioning
confidence: 96%
“…It is an embryologic anomaly, occurring in the eighth week of fetal development, and resulting in non-union of the ventral and dorsal buds. Calculated from autopsy series 4 to 14 per cent (2,3,7,16) of the general population have PD and the corresponding figures from endoscopic retrograde pancreatography (ERP) studies are 1 to 7 per cent (5,6,8). Patients with PD are considered to run a risk of developing pancreatic pain and pancreatitis in the dorsal anlage due to relative outlet obstruction at the minor papilla (5,9,11,15,19,20,23,27).…”
mentioning
confidence: 99%