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A case of ganglioneuromatosis in a child and its outcome
INTRODUCTION: Ganglioneuromas (GNs) are hamartomatous tumors that originate in sympathetic ganglia and adrenal glands. Rarely, they might originate in enteric nervous system affecting its motility. Clinically they present with varying symptoms of pain abdomen, constipation and bleeding. Nevertheless...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220223/ https://www.ncbi.nlm.nih.gov/pubmed/37224724 http://dx.doi.org/10.1016/j.ijscr.2023.108335 |
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author | Aihole, Jayalaxmi Shripati |
author_facet | Aihole, Jayalaxmi Shripati |
author_sort | Aihole, Jayalaxmi Shripati |
collection | PubMed |
description | INTRODUCTION: Ganglioneuromas (GNs) are hamartomatous tumors that originate in sympathetic ganglia and adrenal glands. Rarely, they might originate in enteric nervous system affecting its motility. Clinically they present with varying symptoms of pain abdomen, constipation and bleeding. Nevertheless, patients can remain asymptomatic for many years. CASE PRESENTATION: Author is reporting here a case of ganglioneuromatosis of intestine in a child and its effective management by a simple surgical procedure, yielding good result without morbidity. CLINICAL DISCUSSION: Intestinal ganglioneuromatosis is a rare form of benign neurogenic tumor characterized by hyperplasia of ganglion cell nerve fibers and supporting cells. CONCLUSION: Intestinal ganglioneuromatosis, diagnosed only after histopathological examination, should be managed either by conservative or surgical procedure, depending upon the clinical scenario by attending paediatric surgeon. |
format | Online Article Text |
id | pubmed-10220223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102202232023-05-28 A case of ganglioneuromatosis in a child and its outcome Aihole, Jayalaxmi Shripati Int J Surg Case Rep Case Report INTRODUCTION: Ganglioneuromas (GNs) are hamartomatous tumors that originate in sympathetic ganglia and adrenal glands. Rarely, they might originate in enteric nervous system affecting its motility. Clinically they present with varying symptoms of pain abdomen, constipation and bleeding. Nevertheless, patients can remain asymptomatic for many years. CASE PRESENTATION: Author is reporting here a case of ganglioneuromatosis of intestine in a child and its effective management by a simple surgical procedure, yielding good result without morbidity. CLINICAL DISCUSSION: Intestinal ganglioneuromatosis is a rare form of benign neurogenic tumor characterized by hyperplasia of ganglion cell nerve fibers and supporting cells. CONCLUSION: Intestinal ganglioneuromatosis, diagnosed only after histopathological examination, should be managed either by conservative or surgical procedure, depending upon the clinical scenario by attending paediatric surgeon. Elsevier 2023-05-20 /pmc/articles/PMC10220223/ /pubmed/37224724 http://dx.doi.org/10.1016/j.ijscr.2023.108335 Text en © 2023 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Aihole, Jayalaxmi Shripati A case of ganglioneuromatosis in a child and its outcome |
title | A case of ganglioneuromatosis in a child and its outcome |
title_full | A case of ganglioneuromatosis in a child and its outcome |
title_fullStr | A case of ganglioneuromatosis in a child and its outcome |
title_full_unstemmed | A case of ganglioneuromatosis in a child and its outcome |
title_short | A case of ganglioneuromatosis in a child and its outcome |
title_sort | case of ganglioneuromatosis in a child and its outcome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220223/ https://www.ncbi.nlm.nih.gov/pubmed/37224724 http://dx.doi.org/10.1016/j.ijscr.2023.108335 |
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