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Complete Currarino Triad Presenting With Chronic Constipation

Currarino syndrome (CS) is a congenital disorder that is characterized by the triad of anorectal malformation, sacrococcygeal anomalies, and a presacral mass. The inheritance of CS is autosomal dominant. Chronic constipation is the most common symptom of CS. MRI is considered the most sensitive test...

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Detalles Bibliográficos
Autores principales: Aldabbab, Habib Y, Al Ghadeer, Hussain A, Alnosair, Ashraf A, Al Jabran, Hussain A, Alqattan, Maram H, Abdulrahman, Chadi M, Alabbad, Mohammed R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057639/
https://www.ncbi.nlm.nih.gov/pubmed/35509736
http://dx.doi.org/10.7759/cureus.23743
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author Aldabbab, Habib Y
Al Ghadeer, Hussain A
Alnosair, Ashraf A
Al Jabran, Hussain A
Alqattan, Maram H
Abdulrahman, Chadi M
Alabbad, Mohammed R
author_facet Aldabbab, Habib Y
Al Ghadeer, Hussain A
Alnosair, Ashraf A
Al Jabran, Hussain A
Alqattan, Maram H
Abdulrahman, Chadi M
Alabbad, Mohammed R
author_sort Aldabbab, Habib Y
collection PubMed
description Currarino syndrome (CS) is a congenital disorder that is characterized by the triad of anorectal malformation, sacrococcygeal anomalies, and a presacral mass. The inheritance of CS is autosomal dominant. Chronic constipation is the most common symptom of CS. MRI is considered the most sensitive test to diagnose CS. The report describes an eight-month-old baby girl who presented with chronic constipation. Physical examination showed abdominal distension and anal stenosis. Plain radiographs and MRI revealed sacrococcygeal abnormalities with a presacral mass. A patient was diagnosed with Currarino syndrome and managed surgically with excision of the presacral mass and an anorectoplasty via a posterior sagittal midline incision.
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spelling pubmed-90576392022-05-03 Complete Currarino Triad Presenting With Chronic Constipation Aldabbab, Habib Y Al Ghadeer, Hussain A Alnosair, Ashraf A Al Jabran, Hussain A Alqattan, Maram H Abdulrahman, Chadi M Alabbad, Mohammed R Cureus Pediatrics Currarino syndrome (CS) is a congenital disorder that is characterized by the triad of anorectal malformation, sacrococcygeal anomalies, and a presacral mass. The inheritance of CS is autosomal dominant. Chronic constipation is the most common symptom of CS. MRI is considered the most sensitive test to diagnose CS. The report describes an eight-month-old baby girl who presented with chronic constipation. Physical examination showed abdominal distension and anal stenosis. Plain radiographs and MRI revealed sacrococcygeal abnormalities with a presacral mass. A patient was diagnosed with Currarino syndrome and managed surgically with excision of the presacral mass and an anorectoplasty via a posterior sagittal midline incision. Cureus 2022-04-01 /pmc/articles/PMC9057639/ /pubmed/35509736 http://dx.doi.org/10.7759/cureus.23743 Text en Copyright © 2022, Aldabbab et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatrics
Aldabbab, Habib Y
Al Ghadeer, Hussain A
Alnosair, Ashraf A
Al Jabran, Hussain A
Alqattan, Maram H
Abdulrahman, Chadi M
Alabbad, Mohammed R
Complete Currarino Triad Presenting With Chronic Constipation
title Complete Currarino Triad Presenting With Chronic Constipation
title_full Complete Currarino Triad Presenting With Chronic Constipation
title_fullStr Complete Currarino Triad Presenting With Chronic Constipation
title_full_unstemmed Complete Currarino Triad Presenting With Chronic Constipation
title_short Complete Currarino Triad Presenting With Chronic Constipation
title_sort complete currarino triad presenting with chronic constipation
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057639/
https://www.ncbi.nlm.nih.gov/pubmed/35509736
http://dx.doi.org/10.7759/cureus.23743
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