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Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report

Neuroblastoma is the most common extracranial solid tumor in children, often manifests in the retroperitoneal region. We present a case of a 3-year-old boy with no previous medical history, presented for abdominal distension. Physical examination revealed a distinct, mobile, solid mass situated in t...

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Autores principales: Karray, Amina, Cherifi, Walid, Sassi, Farah, Boussetta, Abir, Haouet, Slim, Gargah, Tahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238441/
https://www.ncbi.nlm.nih.gov/pubmed/37275563
http://dx.doi.org/10.1016/j.eucr.2023.102429
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author Karray, Amina
Cherifi, Walid
Sassi, Farah
Boussetta, Abir
Haouet, Slim
Gargah, Tahar
author_facet Karray, Amina
Cherifi, Walid
Sassi, Farah
Boussetta, Abir
Haouet, Slim
Gargah, Tahar
author_sort Karray, Amina
collection PubMed
description Neuroblastoma is the most common extracranial solid tumor in children, often manifests in the retroperitoneal region. We present a case of a 3-year-old boy with no previous medical history, presented for abdominal distension. Physical examination revealed a distinct, mobile, solid mass situated in the left lumbar region. Abdominal magnetic resonance imaging displayed a well delimited, well-encapsulated mass attached to the tail of the pancreas. Urinary catecholamine metabolite levels were negative. Surgical exploration revealed that the tumor was primitively related to the left adrenal gland, and a complete resection was performed. The postoperative recovery was uncomplicated. NMYC oncogene was non-amplified.
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spelling pubmed-102384412023-06-04 Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report Karray, Amina Cherifi, Walid Sassi, Farah Boussetta, Abir Haouet, Slim Gargah, Tahar Urol Case Rep Pediatrics Neuroblastoma is the most common extracranial solid tumor in children, often manifests in the retroperitoneal region. We present a case of a 3-year-old boy with no previous medical history, presented for abdominal distension. Physical examination revealed a distinct, mobile, solid mass situated in the left lumbar region. Abdominal magnetic resonance imaging displayed a well delimited, well-encapsulated mass attached to the tail of the pancreas. Urinary catecholamine metabolite levels were negative. Surgical exploration revealed that the tumor was primitively related to the left adrenal gland, and a complete resection was performed. The postoperative recovery was uncomplicated. NMYC oncogene was non-amplified. Elsevier 2023-05-21 /pmc/articles/PMC10238441/ /pubmed/37275563 http://dx.doi.org/10.1016/j.eucr.2023.102429 Text en © 2023 The Authors 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 Pediatrics
Karray, Amina
Cherifi, Walid
Sassi, Farah
Boussetta, Abir
Haouet, Slim
Gargah, Tahar
Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report
title Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report
title_full Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report
title_fullStr Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report
title_full_unstemmed Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report
title_short Adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: A case report
title_sort adrenal neuroblastoma in three year old boy, mistaken for pancreatic tumor: a case report
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238441/
https://www.ncbi.nlm.nih.gov/pubmed/37275563
http://dx.doi.org/10.1016/j.eucr.2023.102429
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