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Annular PancreasMayo Clinic Experience From 1957 to 1976 With Review of the Literature
Paul D. Kiernan, MD;
Stephen G. ReMine, MD;
Paul C. Kiernan, MD;
William H. ReMine, MD
Arch Surg. 1980;115(1):46-50.
Abstract
From a review of 266 cases reported in the literature and data on 15 other patients operated on at the Mayo Clinic for symptomatic, annular pancreas, the following three conclusions can be made. First, annular pancreas is an uncommon congenital anomaly, often not becoming symptomatic until late in life. Second, complicating congenital and acquired disorders must be recognized if patients are to be properly prepared for surgery. Sometimes associated problems may be recognized, whereas the annular pancreas may be overlooked. The chance of this happening is decreased by methodical inspection of the entire abdomen, especially all segments of the duodenum, because annuli can occur in any segment and can be partially or completely circumferential. Third, while there is no single operative procedure of choice, published experience militates against any direct attack on the offending annulus.
(Arch Surg 115:46-50, 1980)
Author Affiliations
From the Department of Surgery, Mayo Clinic and Mayo Foundation, Rochester, Minn (Drs Stephen G. ReMine, Paul D. Kiernan, and William H. ReMine); and the Washington Clinic, Washington, DC (Dr Paul C. Kiernan).
Footnotes
Accepted for publication June 29, 1979.
Reprint requests to Section of Publications, Mayo Clinic, 200 First St SW, Rochester, MN 55901 (Dr Paul D. Kiernan).
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