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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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Autor principal: Aihole, Jayalaxmi Shripati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
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.
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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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