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- W1968747877 abstract "Idiopathic retroperitoneal fibrosis (RPF, Ormond’s disease) is characterized by proliferation of fibrous tissue replacing the normal tissue in the central retroperitoneum. Usually the fibrosis involves the area between the renal arteries and sacrum, and causes encasement of the aorta, inferior vena cava (IVC) and ureters, resulting in obstructive hydronephrosis [1–3]. Rare atypical locations of idiopathic RPF involving the pancreas and peripancreatic space, the periduodenal and perirenal space, as well as the pelvis, have been reported [4–7]. Extension of RPF into the mediastinum and peritoneal cavity is also rarely recognized, and its association with sclerosing cholangitis, orbital pseudotumour or chronic thyroiditis suggest an autoimmune basis [8,9]. We present imaging of a case of idiopathic RPF involving the lower mediastinum, the left perirenal space extending to the pelvis along the psoas muscle, and the mesentery. Atypical manifestations of RPF with involvement of other structures at the same time is rare. CASE REPORT" @default.
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- W1968747877 date "2003-04-01" @default.
- W1968747877 modified "2023-09-27" @default.
- W1968747877 title "Uncommon Manifestations of Retroperitoneal Fibrosis" @default.
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- W1968747877 doi "https://doi.org/10.1016/s0009-9260(03)00002-3" @default.
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