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Imperforate anus with a rectovestibular fistula and pseudotail: a case report
INTRODUCTION: Human tails and pseudotails are rare sacrococcygeal lesions that are associated with a wide variety of anomalies and syndromes. Anorectal malformations are also relatively uncommon congenital defects that often occur in conjunction with syndromes or other congenital abnormalities. The...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958973/ https://www.ncbi.nlm.nih.gov/pubmed/20929527 http://dx.doi.org/10.1186/1752-1947-4-317 |
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author | Raines, Miranda D Wills, Marcia L Jackson, Gretchen P |
author_facet | Raines, Miranda D Wills, Marcia L Jackson, Gretchen P |
author_sort | Raines, Miranda D |
collection | PubMed |
description | INTRODUCTION: Human tails and pseudotails are rare sacrococcygeal lesions that are associated with a wide variety of anomalies and syndromes. Anorectal malformations are also relatively uncommon congenital defects that often occur in conjunction with syndromes or other congenital abnormalities. The anomalies associated with both disorders determine the timing and approach to surgical correction. We present an unusual case of a patient with both imperforate anus and a pseudotail in the absence of a syndrome or other associated anomalies and we emphasize the necessity of a thorough preoperative evaluation. CASE PRESENTATION: A Caucasian girl was born at term after an uncomplicated pregnancy and was noted at birth to have a skin-covered posterior midline mass and imperforate anus with a fistula to the vaginal vestibule. Ultrasound and magnetic resonance imaging revealed a predominately fatty lesion without presacral extension and ruled out associated spinal and cord abnormalities. The patient underwent diversion with colostomy and a mucous fistula in the newborn period as a fistulogram demonstrated a long fistulous tract to normal rectum and it was anticipated that anoplasty and resection of the mass would require extensive posterior dissection. The sacrococcygeal mass was removed during posterior sagittal anorectoplasty at the age of six weeks which was determined to be a pseudotail because of the composition of brown fat and cartilage. The patient is now 14 months old with normal bowel function after a colostomy takedown. CONCLUSION: A comprehensive preoperative assessment and thoughtful operative plan were necessary in this unusual case because of the extensive differential diagnosis for sacrococcygeal masses in the newborn and the frequency of anomalies and syndromes associated with tail variants and imperforate anus. The pediatricians and neonatologists who initially evaluate such patients and the surgeons who correct these disorders must be aware of the potential pitfalls in their management. |
format | Text |
id | pubmed-2958973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29589732010-10-22 Imperforate anus with a rectovestibular fistula and pseudotail: a case report Raines, Miranda D Wills, Marcia L Jackson, Gretchen P J Med Case Reports Case Report INTRODUCTION: Human tails and pseudotails are rare sacrococcygeal lesions that are associated with a wide variety of anomalies and syndromes. Anorectal malformations are also relatively uncommon congenital defects that often occur in conjunction with syndromes or other congenital abnormalities. The anomalies associated with both disorders determine the timing and approach to surgical correction. We present an unusual case of a patient with both imperforate anus and a pseudotail in the absence of a syndrome or other associated anomalies and we emphasize the necessity of a thorough preoperative evaluation. CASE PRESENTATION: A Caucasian girl was born at term after an uncomplicated pregnancy and was noted at birth to have a skin-covered posterior midline mass and imperforate anus with a fistula to the vaginal vestibule. Ultrasound and magnetic resonance imaging revealed a predominately fatty lesion without presacral extension and ruled out associated spinal and cord abnormalities. The patient underwent diversion with colostomy and a mucous fistula in the newborn period as a fistulogram demonstrated a long fistulous tract to normal rectum and it was anticipated that anoplasty and resection of the mass would require extensive posterior dissection. The sacrococcygeal mass was removed during posterior sagittal anorectoplasty at the age of six weeks which was determined to be a pseudotail because of the composition of brown fat and cartilage. The patient is now 14 months old with normal bowel function after a colostomy takedown. CONCLUSION: A comprehensive preoperative assessment and thoughtful operative plan were necessary in this unusual case because of the extensive differential diagnosis for sacrococcygeal masses in the newborn and the frequency of anomalies and syndromes associated with tail variants and imperforate anus. The pediatricians and neonatologists who initially evaluate such patients and the surgeons who correct these disorders must be aware of the potential pitfalls in their management. BioMed Central 2010-10-07 /pmc/articles/PMC2958973/ /pubmed/20929527 http://dx.doi.org/10.1186/1752-1947-4-317 Text en Copyright ©2010 Raines et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Raines, Miranda D Wills, Marcia L Jackson, Gretchen P Imperforate anus with a rectovestibular fistula and pseudotail: a case report |
title | Imperforate anus with a rectovestibular fistula and pseudotail: a case report |
title_full | Imperforate anus with a rectovestibular fistula and pseudotail: a case report |
title_fullStr | Imperforate anus with a rectovestibular fistula and pseudotail: a case report |
title_full_unstemmed | Imperforate anus with a rectovestibular fistula and pseudotail: a case report |
title_short | Imperforate anus with a rectovestibular fistula and pseudotail: a case report |
title_sort | imperforate anus with a rectovestibular fistula and pseudotail: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958973/ https://www.ncbi.nlm.nih.gov/pubmed/20929527 http://dx.doi.org/10.1186/1752-1947-4-317 |
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