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10.1007/s13730-014-0117-2 http://scihub22266oqcxt.onion/10.1007/s13730-014-0117-2 C5411567!5411567!28509198     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       CEN+Case+Rep 2014 ; 3 (2): 198-201 Nephropedia Template TP {{tp|p=28509198|t=2014. Localized cystic disease of the kidney: case report and review of the literature |pdf=|usr=}}{{28509198}} gab.com Text Localized cystic disease of the kidney: case report and review of the literature JO: CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=28509198 #FOAvip Localized cystic disease of the kidney (LCDK) is a benign and non-progressive renal anomaly that may initially be confused with autosomal dominant polycystic kidney disease (as in the index case) or cystic neoplasms. It is best diagnosed with contrast-enhanced CT scan demonstrating the characteristic features of an unencapsulated mass of smooth-walled cysts with enhancing renal parenchyma between them. It is most often an incidental finding, but may present with flank pain or haematuria. Hypertension and renal impairment are uncommonly associated with LCDK. A complete physical examination and comprehensive family history are important to exclude other acquired or inherited causes of cystic kidney disease and to avoid unnecessary diagnostic procedures or nephrectomy. We describe a case manifesting many of the typical features of the condition and review previously published cases to describe the natural history and presentation of this rare entity.Electronic supplementary material: The online version of this article (doi:10.1007/s13730-014-0117-2) contains supplementary material, which is available to authorized users. Twit Text FOAVip Localized cystic disease of the kidney: case report and review of the literature ????CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=28509198 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28509198 #FOAvip English Wikipedia <ref>{{Cite pmid|28509198}}</ref> Localized cystic disease of the kidney: case report and review of the literature #MMPMID28509198 Smyth B; Coleman P CEN Case Rep 2014[Nov]; 3 (2): 198-201 PMID28509198show ga Localized cystic disease of the kidney (LCDK) is a benign and non-progressive renal anomaly that may initially be confused with autosomal dominant polycystic kidney disease (as in the index case) or cystic neoplasms. It is best diagnosed with contrast-enhanced CT scan demonstrating the characteristic features of an unencapsulated mass of smooth-walled cysts with enhancing renal parenchyma between them. It is most often an incidental finding, but may present with flank pain or haematuria. Hypertension and renal impairment are uncommonly associated with LCDK. A complete physical examination and comprehensive family history are important to exclude other acquired or inherited causes of cystic kidney disease and to avoid unnecessary diagnostic procedures or nephrectomy. We describe a case manifesting many of the typical features of the condition and review previously published cases to describe the natural history and presentation of this rare entity.Electronic supplementary material: The online version of this article (doi:10.1007/s13730-014-0117-2) contains supplementary material, which is available to authorized users. äLocalized cystic disease of the kidney: case report and review of the (epmc).pdf DeepDyve Pubget Overpricing