Literature DB >> 3487949

The coexistence of congenital megacalyces and primary megaureter.

B Vargas, R L Lebowitz.   

Abstract

Congenital megacalyces is a rare developmental condition of the kidney consisting of hypoplasia of the medullary pyramids and dilatation of the calyces. There is no obstruction. Primary megaureter is a form of obstructive uropathy in which there is an obstructing juxtavesical segment of ureter that is normal in caliber but that is aperistaltic. These conditions were found to occur simultaneously in the same patient six times during the past 10 years. Recognition of this rare coexistence is important so that unnecessary surgery can be avoided.

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Year:  1986        PMID: 3487949     DOI: 10.2214/ajr.147.2.313

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  6 in total

1.  Familial megacalyces with autosomal recessive inheritance. Report of 3 affected siblings.

Authors:  A H Lam
Journal:  Pediatr Radiol       Date:  1988

2.  Schinzel-Giedion syndrome and congenital megacalyces.

Authors:  T E Herman; D A Sweetser; W H McAlister; S B Dowton
Journal:  Pediatr Radiol       Date:  1993

3.  Primary obstructive megaureter in adults: need for an aggressive management strategy.

Authors:  L N Dorairajan; A K Hemal; N P Gupta; S N Wadhwa
Journal:  Int Urol Nephrol       Date:  1999       Impact factor: 2.370

4.  [Post infectious urethral stenosis and megacalycosis: a train that hides another].

Authors:  Babacar Sine; Ndeye Aissatou Bagayogo; Boubacar Fall; Yaya Sow; Amath Thiam; Alioune Sarr; Abdou Razak Hamidou Zakou; Samba Thiapato Faye; Babacar Diao; Papa Ahmed Fall; Alain Khassim Ndoye
Journal:  Pan Afr Med J       Date:  2015-12-04

5.  Radiological findings and the clinical importance of megacalycosis.

Authors:  Christos Kalaitzis; Emmanuel Patris; Evangelia Deligeorgiou; Petros Sountoulides; Athanasios Bantis; Stilianos Giannakopoulos; Stavros Touloupidis
Journal:  Res Rep Urol       Date:  2015-10-19

6.  Schinzel-Giedion Syndrome with Congenital Megacalycosis in a Turkish Patient: Report of SETBP1 Mutation and Literature Review of the Clinical Features.

Authors:  Ozgul Bulut; Zeynep Ince; Umut Altunoglu; Sukran Yildirim; Asuman Coban
Journal:  Case Rep Genet       Date:  2017-12-03
  6 in total

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