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Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature
BACKGROUND: Anal canal duplication (ACD) is a very rare duplication of the gastrointestinal tract and is described as a secondary anal orifice along the posterior side of the normal anal canal. Early surgical removal is advisable, also in asymptomatic patients, because of the risk of inflammatory co...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133505/ https://www.ncbi.nlm.nih.gov/pubmed/35647015 http://dx.doi.org/10.3389/fsurg.2022.908390 |
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author | Li, Dandan Liu, Shuaibin Feng, Jiexiong Yang, Jixin |
author_facet | Li, Dandan Liu, Shuaibin Feng, Jiexiong Yang, Jixin |
author_sort | Li, Dandan |
collection | PubMed |
description | BACKGROUND: Anal canal duplication (ACD) is a very rare duplication of the gastrointestinal tract and is described as a secondary anal orifice along the posterior side of the normal anal canal. Early surgical removal is advisable, also in asymptomatic patients, because of the risk of inflammatory complications, such as recurrent crissum abscess, and malignant changes. CASE PRESENTATION: A previously healthy 2-year-old boy was evaluated in the emergency department with fever. He complained of anal pain in the absence of incentive. Physical examination and ultrasound confirmed a diagnosis of perianal abscess. He was treated with incision and drainage of the abscess and intravenous antibiotics. Two months after his discharge from the hospital, he developed fever and had intervals discharge pus and pain in the same locations. Colorectal endoscopy revealed that there was no fistula opening at the rectal wall. Intraoperative fistulography showed a fistulous tract that was connected to a subcutaneous cavity. Excision of the fistulous tract and wide drainage of the deep postanal space were performed. The patient was referred to our hospital for further evaluation 6 months later. Physical examination showed a secondary anus that had not been noticed before. MRI showed an anal fistula between 1 and 3 o’clock, and preoperative fistulography revealed a 3-cm-long tubular structure without any connection with the rectum. The diagnosis of ACD was made by intraoperative examination with a metal catheter and the postoperative pathological analysis. The duplicated anal canal was resected completely via a perianal approach without any rectal injury. Histology showed a squamous epithelium in the distal end with some smooth-muscle fibers. After a follow-up of 8 months, the patient has been doing well. CONCLUSION: Recurrent crissum abscess should raise clinical attention to alimentary tract congenital malformations such as ACD. Prompt recognition of these unique presentations of ACD is needed, and complete excision through a perineal approach or posterior sagittal approach is recommended. |
format | Online Article Text |
id | pubmed-9133505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91335052022-05-27 Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature Li, Dandan Liu, Shuaibin Feng, Jiexiong Yang, Jixin Front Surg Surgery BACKGROUND: Anal canal duplication (ACD) is a very rare duplication of the gastrointestinal tract and is described as a secondary anal orifice along the posterior side of the normal anal canal. Early surgical removal is advisable, also in asymptomatic patients, because of the risk of inflammatory complications, such as recurrent crissum abscess, and malignant changes. CASE PRESENTATION: A previously healthy 2-year-old boy was evaluated in the emergency department with fever. He complained of anal pain in the absence of incentive. Physical examination and ultrasound confirmed a diagnosis of perianal abscess. He was treated with incision and drainage of the abscess and intravenous antibiotics. Two months after his discharge from the hospital, he developed fever and had intervals discharge pus and pain in the same locations. Colorectal endoscopy revealed that there was no fistula opening at the rectal wall. Intraoperative fistulography showed a fistulous tract that was connected to a subcutaneous cavity. Excision of the fistulous tract and wide drainage of the deep postanal space were performed. The patient was referred to our hospital for further evaluation 6 months later. Physical examination showed a secondary anus that had not been noticed before. MRI showed an anal fistula between 1 and 3 o’clock, and preoperative fistulography revealed a 3-cm-long tubular structure without any connection with the rectum. The diagnosis of ACD was made by intraoperative examination with a metal catheter and the postoperative pathological analysis. The duplicated anal canal was resected completely via a perianal approach without any rectal injury. Histology showed a squamous epithelium in the distal end with some smooth-muscle fibers. After a follow-up of 8 months, the patient has been doing well. CONCLUSION: Recurrent crissum abscess should raise clinical attention to alimentary tract congenital malformations such as ACD. Prompt recognition of these unique presentations of ACD is needed, and complete excision through a perineal approach or posterior sagittal approach is recommended. Frontiers Media S.A. 2022-05-12 /pmc/articles/PMC9133505/ /pubmed/35647015 http://dx.doi.org/10.3389/fsurg.2022.908390 Text en Copyright © 2022 Li, Liu, Feng and Yang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Surgery Li, Dandan Liu, Shuaibin Feng, Jiexiong Yang, Jixin Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature |
title | Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature |
title_full | Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature |
title_fullStr | Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature |
title_full_unstemmed | Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature |
title_short | Anal Canal Duplication Mimicking Recurrent Abscess: A Case Report and Review of the Literature |
title_sort | anal canal duplication mimicking recurrent abscess: a case report and review of the literature |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133505/ https://www.ncbi.nlm.nih.gov/pubmed/35647015 http://dx.doi.org/10.3389/fsurg.2022.908390 |
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