Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization

Neurofibromatosis type I (NF1) is also known as von Recklinghausen disease. It is a genetic disorder that affects the growth and development of nerve cell tissue, which is characterized by a multisystem disorder and an increased risk for cancer. The incidence of gastroduodenal stromal tumor during R...

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Autores principales: Chaka, Amina, Ennaceur, Farouk, Tormen, Mohamed Amine, Korbi, Ibtissem, Noomen, Faouzi, Zouari, Khadija
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553436/
https://www.ncbi.nlm.nih.gov/pubmed/34721919
http://dx.doi.org/10.1155/2021/2868966
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author Chaka, Amina
Ennaceur, Farouk
Tormen, Mohamed Amine
Korbi, Ibtissem
Noomen, Faouzi
Zouari, Khadija
author_facet Chaka, Amina
Ennaceur, Farouk
Tormen, Mohamed Amine
Korbi, Ibtissem
Noomen, Faouzi
Zouari, Khadija
author_sort Chaka, Amina
collection PubMed
description Neurofibromatosis type I (NF1) is also known as von Recklinghausen disease. It is a genetic disorder that affects the growth and development of nerve cell tissue, which is characterized by a multisystem disorder and an increased risk for cancer. The incidence of gastroduodenal stromal tumor during Recklinghausen disease can reach 35% in autopsies and 5% in clinical cases. In our case, the diagnosis of neurofibromatosis type I was made in a middle-aged women initially diagnosed with a pancreaticoduodenal tumor.
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spelling pubmed-85534362021-10-29 Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization Chaka, Amina Ennaceur, Farouk Tormen, Mohamed Amine Korbi, Ibtissem Noomen, Faouzi Zouari, Khadija Case Rep Surg Case Report Neurofibromatosis type I (NF1) is also known as von Recklinghausen disease. It is a genetic disorder that affects the growth and development of nerve cell tissue, which is characterized by a multisystem disorder and an increased risk for cancer. The incidence of gastroduodenal stromal tumor during Recklinghausen disease can reach 35% in autopsies and 5% in clinical cases. In our case, the diagnosis of neurofibromatosis type I was made in a middle-aged women initially diagnosed with a pancreaticoduodenal tumor. Hindawi 2021-10-21 /pmc/articles/PMC8553436/ /pubmed/34721919 http://dx.doi.org/10.1155/2021/2868966 Text en Copyright © 2021 Amina Chaka et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chaka, Amina
Ennaceur, Farouk
Tormen, Mohamed Amine
Korbi, Ibtissem
Noomen, Faouzi
Zouari, Khadija
Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization
title Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization
title_full Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization
title_fullStr Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization
title_full_unstemmed Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization
title_short Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization
title_sort neurofibromatosis type i and stromal tumor with a multiple digestive localization
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553436/
https://www.ncbi.nlm.nih.gov/pubmed/34721919
http://dx.doi.org/10.1155/2021/2868966
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