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Myelomeningocele and Urinary Lithiasis - Case Report

Received: 1 June 2016    Accepted: 25 August 2016    Published: 17 December 2016
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Abstract

Myelomeningocele is a congenital malformation of central nervous system associated with urinary tract anomalies in several cases. This case report describes a 19 years old, female patient, admitted in Santa Casa de Belo Horizonte Hospital where she was previously diagnosed with lumbar myelomeningocele associated, lately, with several kidneys and bladder dysfunctions, including bladder lithiasis, evaluated by laboratory findings, images, and specifics renal depuration tests such as DTPA (diethylenetriaminepentaacetic acid labeled with technetium 99 m) renal scintigraphy. After nephrectomy and antibiotic treatment, the patient had an improvement of her clinical symptoms.

Published in International Journal of Clinical and Experimental Medical Sciences (Volume 2, Issue 6)
DOI 10.11648/j.ijcems.20160206.12
Page(s) 107-109
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Myelomeningocele, Myelomeningocele, Lithiasis

References
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[2] Blok BF, Holstege G. The central control of micturition and continence: implications for urology. BJU Int 1999; 83 (Supp l 2): 1-6.
[3] Lima SV, Araujo LA, Vilar FO, Kummer CL, Lima EC. Combined use of enterocystoplasty and a new type of artificial sphincter in the treatment of urinary incontinence. J Urol 1996;156 (2 Pt 2): 622-4.
[4] Bitsch M, Nerstrom H, Nordling J, Hald T. Upper urinary tract deterioration after implantation of artificial urinary sphincter. Scand J Urol Nephrol 1990; 24: 31-4. 33.
[5] Cole EE, Adams MC, Brock JW 3rd, Pope JC 4th. Outcome of continence procedures in the pediatric patient: a single institutional experience. J Urol 2003; 170(2 Pt 1): 560-3.
[6] Johnson HW, Weckworth PF, Coleman GU, Arnold WJ, Sawatzky BJ, Moloney PJ, et al. Bladder-outlet reconstruction in neurogenic bladder due to myelomeningocele. Can J Surg 1988; 31: 22-24.
[7] Kropp KA, Angwafo FF. Urethral lengthening and reimplantation for neurogenic incontinence in children. J Urol 1986; 135: 533-6.
[8] Verdu T, Salinas Casado J, Herranz Amo F, Diez Cordero JM, Duran Merino R, Hernandez Fernandez C. Urinary calculi in myelomeningocele adults. Actas Urol Esp. 2006; 30 (7): 675-683.
[9] Kyrklund K, Pakarinen MP, Taskinen S, Kivisaari R, Rintala RJ. Spinal cord anomalies in patients with anorectal malformations without severe sacral abnormalities or meningomyelocele: outcomes after expectant, conservative management. J Neurosurg Spine. 2016; 1-8.
[10] North, WD, Khoury L, Christopher R, Liau JY, Pittman T. Use of dermal regeneration template to close a giant myelomeningocele in a newborn. J Neurosurg Pediatr. 2016; 1-3.
[11] Baghdadi, T, Abdi R, Bashi RZ, Aslani H. Surgical Management of Hip Problems in Myelomeningocele: A Review Article. Arch Bone Jt Surg. 2016; 4 (3): 197-203.
Cite This Article
  • APA Style

    Rogério Saint-Clair Pimentel Mafra, Rafael Morroni de Oliveira, Arthur Guilherme Lobato de Castro, Luiz Ronaldo Alberti. (2016). Myelomeningocele and Urinary Lithiasis - Case Report. International Journal of Clinical and Experimental Medical Sciences, 2(6), 107-109. https://doi.org/10.11648/j.ijcems.20160206.12

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    ACS Style

    Rogério Saint-Clair Pimentel Mafra; Rafael Morroni de Oliveira; Arthur Guilherme Lobato de Castro; Luiz Ronaldo Alberti. Myelomeningocele and Urinary Lithiasis - Case Report. Int. J. Clin. Exp. Med. Sci. 2016, 2(6), 107-109. doi: 10.11648/j.ijcems.20160206.12

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    AMA Style

    Rogério Saint-Clair Pimentel Mafra, Rafael Morroni de Oliveira, Arthur Guilherme Lobato de Castro, Luiz Ronaldo Alberti. Myelomeningocele and Urinary Lithiasis - Case Report. Int J Clin Exp Med Sci. 2016;2(6):107-109. doi: 10.11648/j.ijcems.20160206.12

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  • @article{10.11648/j.ijcems.20160206.12,
      author = {Rogério Saint-Clair Pimentel Mafra and Rafael Morroni de Oliveira and Arthur Guilherme Lobato de Castro and Luiz Ronaldo Alberti},
      title = {Myelomeningocele and Urinary Lithiasis - Case Report},
      journal = {International Journal of Clinical and Experimental Medical Sciences},
      volume = {2},
      number = {6},
      pages = {107-109},
      doi = {10.11648/j.ijcems.20160206.12},
      url = {https://doi.org/10.11648/j.ijcems.20160206.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcems.20160206.12},
      abstract = {Myelomeningocele is a congenital malformation of central nervous system associated with urinary tract anomalies in several cases. This case report describes a 19 years old, female patient, admitted in Santa Casa de Belo Horizonte Hospital where she was previously diagnosed with lumbar myelomeningocele associated, lately, with several kidneys and bladder dysfunctions, including bladder lithiasis, evaluated by laboratory findings, images, and specifics renal depuration tests such as DTPA (diethylenetriaminepentaacetic acid labeled with technetium 99 m) renal scintigraphy. After nephrectomy and antibiotic treatment, the patient had an improvement of her clinical symptoms.},
     year = {2016}
    }
    

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    AU  - Rafael Morroni de Oliveira
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    AB  - Myelomeningocele is a congenital malformation of central nervous system associated with urinary tract anomalies in several cases. This case report describes a 19 years old, female patient, admitted in Santa Casa de Belo Horizonte Hospital where she was previously diagnosed with lumbar myelomeningocele associated, lately, with several kidneys and bladder dysfunctions, including bladder lithiasis, evaluated by laboratory findings, images, and specifics renal depuration tests such as DTPA (diethylenetriaminepentaacetic acid labeled with technetium 99 m) renal scintigraphy. After nephrectomy and antibiotic treatment, the patient had an improvement of her clinical symptoms.
    VL  - 2
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Author Information
  • Santa Casa de Belo Horizonte Hospital and FAMINAS BH, Faculty of Medicine, Belo Horizonte, Brazil

  • Santa Casa de Belo Horizonte Hospital, Belo Horizonte, Brazil

  • FAMINAS-BH – Faculty of Medicine, Belo Horizonte, Bazil

  • Santa Casa de Belo Horizonte Hospital and UFMG, Department of Surgery, Faculty of Medicine, Belo Horizonte, Brazil

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