Literature DB >> 15963135

Upper and lower urinary tract outcome after surgical repair of cloacal malformations: a three-decade experience.

Richard C Rink1, C D Anthony Herndon, Mark P Cain, Martin Kaefer, Andrew M Dussinger, Shelly J King, Anthony J Casale.   

Abstract

OBJECTIVE: To report the urological outcome of the surgical correction of persistent cloaca, which is technically demanding and may require many procedures in an effort to preserve renal function and provide urinary continence. PATIENTS AND METHODS: A retrospective chart review from 1971 to 2003 identified 23 patients with cloacal malformations (two posterior, 21 classical) that were reconstructed. The confluence of the urethra, vagina and rectum was noted to be high in 16, low in five and unknown in two; one patient was a conjoined twin.
RESULTS: The mean (range) follow-up was 9.3 (0.4-31.6) years. Urinary anomalies included 14 patients with renal anomalies (six solitary kidneys, four renal dysplasia, two pelvi-ureteric junction, one each duplex and crossed fused) and two duplicated bladders. Vesico-ureteric reflux was present in 13 patients (57%), hydronephrosis at birth in 13, a bony vertebral abnormality in 14 and the VACTERL association in four. Total urogenital mobilization (TUM) was used in six patients and spinal cord untethering in four; a nephrectomy was required in three and partial nephrectomy in one. Upper tract dilation was still present in six patients. Age-adjusted creatinine levels were abnormal in four (18%) patients and borderline in another six (26%). In the nine patients with a solitary kidney (six solitary, three after nephrectomy), the age-adjusted creatinine level was abnormal in two and borderline in four. A vesicostomy was initially performed in 11 patients. The method of bladder emptying is known in 22; 10 void, 11 require clean intermittent catheterization (five abdominal stoma, six urethral) and one was diverted with a conduit. Of the 18 patients aged > 47 months 15 were continent (14 complete > 4 h, one partial 2-4 h), and three are wet (one conduit). Reconstruction of the lower urinary tract included four bladder augmentations (one ureteric, one ileal, two colon), five bladder neck procedures (two artificial sphincter, one each bladder neck repair, sling, bladder neck division) and six catheterizable channels (one now with a colon conduit). The ureters were re-implanted in 12 patients.
CONCLUSION: Although the surgical correction of this rare malformation is complex, the upper urinary and lower urinary tract outcome can be favourable, albeit after several reconstructive procedures. TUM has emerged as the primary method for vaginal reconstruction, but the long-term lower tract outcome after this procedure is awaited.

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Year:  2005        PMID: 15963135     DOI: 10.1111/j.1464-410X.2005.05581.x

Source DB:  PubMed          Journal:  BJU Int        ISSN: 1464-4096            Impact factor:   5.588


  7 in total

Review 1.  Are children with congenital solitary kidney at risk for lifelong complications? A lack of prediction demands caution.

Authors:  Marco Zaffanello; Milena Brugnara; Michele Zuffante; Massimo Franchini; Vassilios Fanos
Journal:  Int Urol Nephrol       Date:  2008-08-09       Impact factor: 2.370

2.  Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.

Authors:  Phyllis W Speiser; Ricardo Azziz; Laurence S Baskin; Lucia Ghizzoni; Terry W Hensle; Deborah P Merke; Heino F L Meyer-Bahlburg; Walter L Miller; Victor M Montori; Sharon E Oberfield; Martin Ritzen; Perrin C White
Journal:  J Clin Endocrinol Metab       Date:  2010-09       Impact factor: 5.958

3.  Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations.

Authors:  Dagan Jenkins; Maria Bitner-Glindzicz; Louise Thomasson; Sue Malcolm; Stephanie A Warne; Sally A Feather; Sarah E Flanagan; Sian Ellard; Coralie Bingham; Lane Santos; Mark Henkemeyer; Andrew Zinn; Linda A Baker; Duncan T Wilcox; Adrian S Woolf
Journal:  J Pediatr Urol       Date:  2007-02       Impact factor: 1.830

4.  Long-term renal function and continence status in patients with cloacal malformation.

Authors:  Luis H P Braga; Armando J Lorenzo; Sumit Dave; Maria H Del-Valle; Antoine E Khoury; Joao L Pippi-Salle
Journal:  Can Urol Assoc J       Date:  2007-11       Impact factor: 1.862

5.  Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.

Authors:  Phyllis W Speiser; Wiebke Arlt; Richard J Auchus; Laurence S Baskin; Gerard S Conway; Deborah P Merke; Heino F L Meyer-Bahlburg; Walter L Miller; M Hassan Murad; Sharon E Oberfield; Perrin C White
Journal:  J Clin Endocrinol Metab       Date:  2018-11-01       Impact factor: 5.958

6.  Urogenital Management in Cloaca: An Alternative Approach.

Authors:  Harshjeet Singh Bal; Sudipta Sen; Cenita Sam; Jacob Chacko; John Mathai; S R Regunandan
Journal:  J Indian Assoc Pediatr Surg       Date:  2017 Apr-Jun

7.  An Unusual Case of Type A Posterior Cloaca Associated with 46XX Disorder of Sexual Differentiation with Y Duplication of Urethra.

Authors:  Rahul K Gupta; Pooja Tiwari; Sandesh V Parelkar; Beejal V Sanghvi; Kedar P Mudkhedkar; Satej S Mhaskar; Rujuta S Shah
Journal:  J Indian Assoc Pediatr Surg       Date:  2022-03-01
  7 in total

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