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Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report
BACKGROUND: Various terms have been used to describe vascular lesions in the intestine, including angiodysplasia, arteriovenous malformation, and telangiectasia. Such lesions are common in adults and are typified by angiodysplasia, a type of arteriovenous malformation. In contrast, these lesions are...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142189/ https://www.ncbi.nlm.nih.gov/pubmed/32270382 http://dx.doi.org/10.1186/s40792-020-00824-x |
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author | Kido, Miori Nakamura, Kiyokuni Kuwahara, Tsuyoshi Yasui, Yoshitomo Okajima, Hideaki Kurose, Nozomu Kohno, Miyuki |
author_facet | Kido, Miori Nakamura, Kiyokuni Kuwahara, Tsuyoshi Yasui, Yoshitomo Okajima, Hideaki Kurose, Nozomu Kohno, Miyuki |
author_sort | Kido, Miori |
collection | PubMed |
description | BACKGROUND: Various terms have been used to describe vascular lesions in the intestine, including angiodysplasia, arteriovenous malformation, and telangiectasia. Such lesions are common in adults and are typified by angiodysplasia, a type of arteriovenous malformation. In contrast, these lesions are rarely seen in the pediatric population. Angiodysplasia may cause gastrointestinal bleeding, which is sometimes an indication for treatment. Considering the high rate of recurrence after surgical treatment, conservative treatments are mainly chosen. We herein report an extremely rare case of a prolapsed colon due to an arteriovenous malformation successfully treated by resection in a 1-year-old girl. We also highlight the differences between pediatric and adult cases. CASE PRESENTATION: A girl developed bloody stools at 7 months of age. She visited another hospital at 1 year of age because of continuing moderate hematochezia and recent onset of rectal prolapse. Colonoscopy showed a protruding lesion located 15 cm from the anal verge, suggesting a submucosal vascular abnormality. Contrast-enhanced computed tomography and magnetic resonance imaging at our hospital revealed the localized lesion with dilated blood vessels in part of the sigmoid colon; no other lesions were present in the gastrointestinal tract. Laparoscopic-assisted sigmoidectomy was performed. A subserosal vascular lesion was visualized and resected using end-to-end anastomosis. Pathologic examination of the 2.2 × 2.7-cm segment revealed several abnormally enlarged and ectatic blood vessels in the submucosa extending into the subserosa. The lesion was diagnosed as an arteriovenous malformation. The patient had a good clinical course without recurrence at the 2-year follow-up. CONCLUSIONS: An arteriovenous malformation in the sigmoid colon may rarely cause intussusception and prolapse of the colon. Complete resection is a radical and potentially effective treatment. Computed tomography and colonoscopy were useful for evaluation of the lesion in the present case. |
format | Online Article Text |
id | pubmed-7142189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-71421892020-04-15 Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report Kido, Miori Nakamura, Kiyokuni Kuwahara, Tsuyoshi Yasui, Yoshitomo Okajima, Hideaki Kurose, Nozomu Kohno, Miyuki Surg Case Rep Case Report BACKGROUND: Various terms have been used to describe vascular lesions in the intestine, including angiodysplasia, arteriovenous malformation, and telangiectasia. Such lesions are common in adults and are typified by angiodysplasia, a type of arteriovenous malformation. In contrast, these lesions are rarely seen in the pediatric population. Angiodysplasia may cause gastrointestinal bleeding, which is sometimes an indication for treatment. Considering the high rate of recurrence after surgical treatment, conservative treatments are mainly chosen. We herein report an extremely rare case of a prolapsed colon due to an arteriovenous malformation successfully treated by resection in a 1-year-old girl. We also highlight the differences between pediatric and adult cases. CASE PRESENTATION: A girl developed bloody stools at 7 months of age. She visited another hospital at 1 year of age because of continuing moderate hematochezia and recent onset of rectal prolapse. Colonoscopy showed a protruding lesion located 15 cm from the anal verge, suggesting a submucosal vascular abnormality. Contrast-enhanced computed tomography and magnetic resonance imaging at our hospital revealed the localized lesion with dilated blood vessels in part of the sigmoid colon; no other lesions were present in the gastrointestinal tract. Laparoscopic-assisted sigmoidectomy was performed. A subserosal vascular lesion was visualized and resected using end-to-end anastomosis. Pathologic examination of the 2.2 × 2.7-cm segment revealed several abnormally enlarged and ectatic blood vessels in the submucosa extending into the subserosa. The lesion was diagnosed as an arteriovenous malformation. The patient had a good clinical course without recurrence at the 2-year follow-up. CONCLUSIONS: An arteriovenous malformation in the sigmoid colon may rarely cause intussusception and prolapse of the colon. Complete resection is a radical and potentially effective treatment. Computed tomography and colonoscopy were useful for evaluation of the lesion in the present case. Springer Berlin Heidelberg 2020-04-08 /pmc/articles/PMC7142189/ /pubmed/32270382 http://dx.doi.org/10.1186/s40792-020-00824-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Case Report Kido, Miori Nakamura, Kiyokuni Kuwahara, Tsuyoshi Yasui, Yoshitomo Okajima, Hideaki Kurose, Nozomu Kohno, Miyuki Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report |
title | Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report |
title_full | Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report |
title_fullStr | Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report |
title_full_unstemmed | Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report |
title_short | Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report |
title_sort | arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142189/ https://www.ncbi.nlm.nih.gov/pubmed/32270382 http://dx.doi.org/10.1186/s40792-020-00824-x |
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