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Appendicitis and ganglioneuroma—an unusual co-existence

Ganglioneuromas are benign, fully differentiated mature tumours related to neuronal tissues and usually seen in the gastrointestinal tract, retroperitoneum and mediastinum. The few cases of appendiceal ganglioneuromas that were previously described in the literature belong to the paediatric populati...

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Autores principales: Koullouros, Michalis, Candler, Sarah, Smith, Caroline, Olakkengil, Santosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784186/
https://www.ncbi.nlm.nih.gov/pubmed/35079345
http://dx.doi.org/10.1093/jscr/rjab632
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author Koullouros, Michalis
Candler, Sarah
Smith, Caroline
Olakkengil, Santosh
author_facet Koullouros, Michalis
Candler, Sarah
Smith, Caroline
Olakkengil, Santosh
author_sort Koullouros, Michalis
collection PubMed
description Ganglioneuromas are benign, fully differentiated mature tumours related to neuronal tissues and usually seen in the gastrointestinal tract, retroperitoneum and mediastinum. The few cases of appendiceal ganglioneuromas that were previously described in the literature belong to the paediatric population and were associated with genetic mutations and syndromes. We present a unique case of an Aboriginal Australian adult with acute appendicitis and concurrent ganglioneuroma diagnosed using histopathology and immunohistochemistry using Neu-N, S100 and Sox-10. The patient had no history of any of the syndromes associated with ganglioneuromatosis and had no other relevant family history.
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spelling pubmed-87841862022-01-24 Appendicitis and ganglioneuroma—an unusual co-existence Koullouros, Michalis Candler, Sarah Smith, Caroline Olakkengil, Santosh J Surg Case Rep Case Report Ganglioneuromas are benign, fully differentiated mature tumours related to neuronal tissues and usually seen in the gastrointestinal tract, retroperitoneum and mediastinum. The few cases of appendiceal ganglioneuromas that were previously described in the literature belong to the paediatric population and were associated with genetic mutations and syndromes. We present a unique case of an Aboriginal Australian adult with acute appendicitis and concurrent ganglioneuroma diagnosed using histopathology and immunohistochemistry using Neu-N, S100 and Sox-10. The patient had no history of any of the syndromes associated with ganglioneuromatosis and had no other relevant family history. Oxford University Press 2022-01-22 /pmc/articles/PMC8784186/ /pubmed/35079345 http://dx.doi.org/10.1093/jscr/rjab632 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2022. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Koullouros, Michalis
Candler, Sarah
Smith, Caroline
Olakkengil, Santosh
Appendicitis and ganglioneuroma—an unusual co-existence
title Appendicitis and ganglioneuroma—an unusual co-existence
title_full Appendicitis and ganglioneuroma—an unusual co-existence
title_fullStr Appendicitis and ganglioneuroma—an unusual co-existence
title_full_unstemmed Appendicitis and ganglioneuroma—an unusual co-existence
title_short Appendicitis and ganglioneuroma—an unusual co-existence
title_sort appendicitis and ganglioneuroma—an unusual co-existence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784186/
https://www.ncbi.nlm.nih.gov/pubmed/35079345
http://dx.doi.org/10.1093/jscr/rjab632
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