Flexible ureteroscopic management of symptomatic renal cystic diseases

2015 ◽  
Vol 196 (1) ◽  
pp. 118-123 ◽  
Author(s):  
Weiwen Yu ◽  
Dahong Zhang ◽  
Xiang He ◽  
Yuelong Zhang ◽  
Guodong Liao ◽  
...  
1999 ◽  
Vol 161 (4) ◽  
pp. 1404-1404
Author(s):  
E.A.P. Reichard ◽  
M.A. Roubidoux ◽  
N.R. Dunnick

Author(s):  
Alexandra Rehfuss ◽  
Christina Ching ◽  
Daniel DaJusta ◽  
Molly Fuchs

1979 ◽  
Vol 5 (5) ◽  
pp. 289-293
Author(s):  
J. Bruezière

2012 ◽  
Vol 303 (8) ◽  
pp. C862-C871 ◽  
Author(s):  
Vinita Takiar ◽  
Kavita Mistry ◽  
Monica Carmosino ◽  
Nicole Schaeren-Wiemers ◽  
Michael J. Caplan

The polarized organization of epithelial cells is required for vectorial solute transport and may be altered in renal cystic diseases. Vesicle integral protein of 17 kDa (VIP17/MAL) is involved in apical vesicle transport. VIP17/MAL overexpression in vivo results in renal cystogenesis of unknown etiology. Renal cystogenesis can occur as a consequence of defects of the primary cilium. To explore the role of VIP17/MAL in renal cystogenesis and ciliogenesis, we examined the polarization and ciliary morphology of wild-type and VIP17/MAL overexpressing Madin-Darby canine kidney renal epithelial cells grown in two-dimensional (2D) and three-dimensional (3D) cyst culture. VIP17/MAL is apically localized when expressed in cells maintained in 2D and 3D culture. VIP17/MAL overexpressing cells produce more multilumen cysts compared with controls. While the distributions of basolateral markers are not affected, VIP17/MAL expression results in aberrant sorting of the apical marker gp135 to the primary cilium. VIP17/MAL overexpression is also associated with shortened or absent cilia. Immunofluorescence analysis performed on kidney sections from VIP17/MAL transgenic mice also demonstrates fewer and shortened cilia within dilated lumens ( P < 0.01). These studies demonstrate that VIP17/MAL overexpression results in abnormal cilium and cyst development, in vitro and in vivo, suggesting that VIP17/MAL overexpressing mice may develop cysts secondary to a ciliary defect.


1999 ◽  
pp. 1404
Author(s):  
E. A. P. Reichard ◽  
M. A. Roubidoux ◽  
N. R. Dunnick

1997 ◽  
Vol 7 (8) ◽  
pp. 1267-1275 ◽  
Author(s):  
H. S. Thomsen ◽  
E. Levine ◽  
J. W. Meilstrup ◽  
M. A. Van Slyke ◽  
K. A. Edgar ◽  
...  

2012 ◽  
Vol 136 (4) ◽  
pp. 400-409 ◽  
Author(s):  
Ying-Bei Chen ◽  
Satish K. Tickoo

Context.—Cystic lesions of the kidney may be accompanied by a range of neoplasms with distinct prognoses and future risks of developing additional tumors. In addition, some renal tumors, with or without accompanying renal cysts, may show a prominent cystic component. In the adult population, neoplasms occurring in a background of renal cystic diseases and cystic renal neoplasms often pose diagnostic challenges because of their many overlapping features. Objective.—To review the clinicopathologic characteristics of common entities in the spectrum of neoplastic and potential preneoplastic cystic lesions encountered in adults, with an emphasis on renal cystic diseases associated with tumor development and on renal neoplasms with predominantly cystic morphology. Data Sources.—The relevant English-language literature was reviewed, accompanied by the authors' experience at their practicing institution. Conclusions.—The presence of multiple renal cysts, both acquired and syndromic, can be associated with a variety of renal tumors. The morphology of the cysts and associated tumor types can help predict the genetic or acquired basis of the lesions, and particularly in specimens with no accompanying pertinent clinical history, such potential associations should be suggested in surgical pathology reports.


2006 ◽  
Vol 13 (1) ◽  
pp. 26-56 ◽  
Author(s):  
Michele Bisceglia ◽  
Carlos A Galliani ◽  
Christof Senger ◽  
Carmine Stallone ◽  
Adalberto Sessa

2012 ◽  
pp. 319-333
Author(s):  
Lesley Rees ◽  
Paul A. Brogan ◽  
Detlef Bockenhauer ◽  
Nicholas J.A. Webb

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