medigraphic.com
SPANISH

Revista Médica Sinergia

Revista Médica Sinergia
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2020, Number 11

<< Back Next >>

Revista Médica Sinergia 2020; 5 (11)

Prune Belly syndrome

Arias VR, Herrera WG, Lobo PT
Full text How to cite this article

Language: Spanish
References: 20
Page: 1-9
PDF size: 171.05 Kb.


Key words:

Prune Belly syndrome, cryptorchidism, abdominal wall, urinary tract, urinary bladder, children.

ABSTRACT

Prune Belly syndrome or Eagle-Barrett syndrome is a rare congenital disorder, with unknown etiology, characterized by the clinical triad of abdominal wall musculature hypoplasia, cryptorchidism and urinary tract malformations. Clinical presentation is variable, depending on the severity of urinary tract malformations and renal compromise. Diagnosis is usually through prenatal echography or evident at birth. Treatment of Prune Belly syndrome is primarily conservative, and surgical management depends upon the severity of symptoms, ranging from modest to more extensive procedures.


REFERENCES

  1. Achour R, Bennour W, Ksibi I, Cheour M, Hamila T, Hmid B et al. Prune belly syndrome: Approaches to its diagnosis and management. Intractable Rare Dis Res. 2018;7(4):271-4. https://doi.org/10.5582/irdr.2018.01094

  2. Arlen A, Nawaf C, Kirsch A. Prune belly syndrome: current perspectives. Pediatr Heal Med Ther. 2019. 10(1):75-81. https://doi.org/10.2147/PHMT.S188014

  3. Ferrer R, Vásquez R, Madiedo D. Síndrome de Prune Belly: Revisión Bibliográfica. Multimed. 2016; 20(4):831-8.

  4. Alkhamis W, Abdulghani S, Altaki A. Challenging diagnosis of Prune belly syndrome antenatally: A case report. J Med Case Rep. 2019;13(1):1-6. https://doi.org/10.1186/s13256-019-2120-x

  5. Joseph D. Prune Belly Syndrome. In: Barakat A, Rushton G (eds). Congenital Anomalies of the Kidney and Urinary Tract. 1st ed. Switzerland: Springer International Publishing; 2016. p. 197-213. https://doi.org/10.1007/978-3-319-29219-9_10

  6. Samal S, Rathod S. Prune Belly syndrome: A rare case report. J Nat Sci Biol Med. 2015;6(1):255. https://doi.org/10.4103/0976-9668.149218

  7. Abdelmoneim K, Eltigani Ali, Safaa M, Huda M. Prune belly syndrome: A report of 15 cases from Sudan. Sudan J Paediatr. 2017; 17 (1): 42-48. https://doi.org/10.24911/SJP.2017.2.5

  8. Solarin A, Disu E, Gbelee H, Animashaun A, Aremu O, Ogbuokiri E, et al. Three Cases of Prune Belly Syndrome at the Lagos State University Teaching Hospital, Ikeja. Saudi J Kidney Dis Transpl. 2018;29(1):178-184.https://doi.org/10.4103/1319-2442.225190

  9. Staatz G, Rascher W. Imaging in Prune Belly Syndrome and Other Syndromes Affecting the Urogenital Tract. In: Riccabona M (eds). Pediatric Urogenital Radiology. 1st ed. Switzerland: Springer International Publishing; 2018. p. 481-490. https://doi.org/10.1007/978-3-319-39202-8_27

  10. Boghossian NS, Sicko RJ, Giannakou A, Dimopoulos A, Caggana M, Tsai MY et al. Rare copy number variants identified in Prune belly syndrome. Eur J Med Genet. 2018;61(3):145-51. https://doi.org/10.1016/j.ejmg.2017.11.008

  11. Keet K, Michael B, Tubbs S. Prune-belly syndrome in Africa: An analysis and systematic review of cases, etiology, treatment, and outcomes. J Clin Urol. 2019. https://doi.org/10.1177/2051415820903196

  12. Cornel A, Duicu C, Delean D, Bulata B, Starcea M. Long term follow-up in a patient with prune-belly syndrome - a care compliant case report. Medicine. 2019; 98(33): e16745. https://doi.org/10.1097/MD.0000000000016745

  13. Brewer F, Harper I. Prune-Belly Syndrome. In Copel J Obstetric Imaging: Fetal Diagnosis. 2nd ed. Philadelphia: Elsevier Health Sciences; 2017. p. 574-576. https://doi.org/10.1016/B978-0-323-44548- 1.00139-X

  14. Demisse A, Berhanu A, Tadesse T. Unusual presentation of Prune belly syndrome: a case report. J Med Case Rep. 2017; 11:337. https://doi.org/10.1186/s13256-017-1487-9

  15. Gupta A, Sehgal R, Vasdev N, Mehta S, Sain P. Antenatal Diagnosis of Prune Belly Syndrome. J. Fetal Med. 2016. https://doi.org/10.1007/s40556-016-0085-z

  16. Chhabra R, Awan A, Stapleton C, Cavalleri G, Conlon P. Clinical manifestations of Prune belly síndrome. Clin Med. 2016; 16(3). https://doi.org/10.7861/clinmedicine.16-3-s5

  17. Wong DG, Arevalo MK, Passoni NM, Iqbal NS, Jascur T, Kern AJ, et al. Phenotypic severity scoring system and categorisation for Prune belly syndrome: application to a pilot cohort of 50 living patients. BJU Int. 2019;123(1):130-9. https://doi.org/10.1111/bju.14524

  18. White J, Sheth K, Bilgutay A, Roth D, Austin P, Gonzales E et al. Vesicoamniotic Shunting Improves Outcomes in a Subset of Prune Belly Syndrome Patients at a Single Tertiary Center. Front Pediatr. 2018; 6:180. https://doi.org/10.3389/fped.2018.00180

  19. Selvi I, Baydilli N, Akınsal E. A rare case: Congenital Megalourethra in prune belly syndrome. Arch Case Rep. 2018; 2: 001-003. https://doi.org/10.29328/journal.acr.1001005

  20. Redondo Y, Ruiz O, Ramírez R, Venegas R. Síndrome Prune Belly: sobrevida de un paciente con insuficiencia Renal. Pediatr. 2017; 50(3):78-81. https://doi.org/10.14295/pediatr.v50i3.69




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Revista Médica Sinergia. 2020;5