scholarly journals Retroperitoneal fibrosis on intravenous pyelogram

2013 ◽  
Author(s):  
Tim Luijkx ◽  
Jan Gerstenmaier
2020 ◽  
Vol 8 (1) ◽  
pp. 101-107
Author(s):  
S.V. Shchekaturov ◽  
◽  
M.M. Kaabak ◽  
A.K. Zokoev ◽  
E.R. Charchyan ◽  
...  

2019 ◽  
Author(s):  
Agnieszka Jarzynska ◽  
Huma Humayun Khan ◽  
Shanthi Chandran

1995 ◽  
Vol 164 (2) ◽  
pp. 515-516 ◽  
Author(s):  
R M Spillane ◽  
G J Whitman

2021 ◽  
Vol 23 (3) ◽  
Author(s):  
Paride Fenaroli ◽  
Federica Maritati ◽  
Augusto Vaglio

2021 ◽  
Vol 9 ◽  
pp. 2050313X2110169
Author(s):  
Kim Rouven Liedtke ◽  
Christoph Käding ◽  
Paula Döring ◽  
Sander Bekeschus ◽  
Anne Susann Glitsch

Several chronic inflammatory diseases have been found to be a subtype of IgG4-related disease, all of which have a typical clinical and histological change, which is based in particular on an overexpression of IgG4 and subsequent fibrosis. At least a part of the retroperitoneal fibrosis, which was originally classified as idiopathic, seems to be assigned to IgG4-related disease. Lymphangiomas are benign, cystic tumors that rarely occur in adults. However, there is no firm association with IgG4-related disease described in the literature to date. This report is about a patient suffering from acute renal failure due to a giant retroperitoneal cyst. Surgical resection remains incomplete in the iliac vessel area due to severe fibrosis and histology revealed features of both lymphangioma and IgG4+ fibrosis. The case description is followed by a brief overview of IgG4-related disease and a consideration of whether lymphangiomas might be assigned to this topic.


2005 ◽  
Vol 35 (1) ◽  
pp. 43-48 ◽  
Author(s):  
Antonella Afeltra ◽  
Umberto Vespasiani Gentilucci ◽  
Carla Rabitti ◽  
Antonio Amoroso ◽  
Marco Caricato ◽  
...  

1983 ◽  
Vol 76 (12) ◽  
pp. 1023-1025 ◽  
Author(s):  
C D M Fletcher ◽  
P E M Jarrett

Idiopathic retroperitoneal fibrosis is uncommon enough to be placed low down on a list of differential diagnoses of any problem facing a general surgeon in a district hospital. In this paper, 4 cases of retroperitoneal fibrosis are described, all of whom presented within a 5-year period to the same surgeon; each described a different symptomatology. This paper serves to reiterate the diversity of presenting features in retroperitoneal fibrosis and to demonstrate that this condition may not be as rare as is widely believed.


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