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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| Format: | Article |
| Language: | English |
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Wiley
2021-01-01
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| Series: | Case Reports in Surgery |
| Online Access: | http://dx.doi.org/10.1155/2021/2868966 |
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| author | Amina Chaka Farouk Ennaceur Mohamed Amine Tormen Ibtissem Korbi Faouzi Noomen Khadija Zouari |
| author_facet | Amina Chaka Farouk Ennaceur Mohamed Amine Tormen Ibtissem Korbi Faouzi Noomen Khadija Zouari |
| author_sort | Amina Chaka |
| collection | DOAJ |
| 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. |
| format | Article |
| id | doaj-art-ec4d7b33070c4eabb305865cc29b362d |
| institution | Kabale University |
| issn | 2090-6900 2090-6919 |
| language | English |
| publishDate | 2021-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Case Reports in Surgery |
| spelling | doaj-art-ec4d7b33070c4eabb305865cc29b362d2025-02-03T05:45:20ZengWileyCase Reports in Surgery2090-69002090-69192021-01-01202110.1155/2021/28689662868966Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive LocalizationAmina Chaka0Farouk Ennaceur1Mohamed Amine Tormen2Ibtissem Korbi3Faouzi Noomen4Khadija Zouari5Department of General and Digestive Surgery at the University Hospital Fattouma Bourguiba of Monastir, University of Monastir, TunisiaDepartment of General and Digestive Surgery at the University Hospital Fattouma Bourguiba of Monastir, University of Monastir, TunisiaDepartment of General and Digestive Surgery at the University Hospital Fattouma Bourguiba of Monastir, University of Monastir, TunisiaDepartment of General and Digestive Surgery at the University Hospital Fattouma Bourguiba of Monastir, University of Monastir, TunisiaDepartment of General and Digestive Surgery at the University Hospital Fattouma Bourguiba of Monastir, University of Monastir, TunisiaDepartment of General and Digestive Surgery at the University Hospital Fattouma Bourguiba of Monastir, University of Monastir, TunisiaNeurofibromatosis 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.http://dx.doi.org/10.1155/2021/2868966 |
| spellingShingle | Amina Chaka Farouk Ennaceur Mohamed Amine Tormen Ibtissem Korbi Faouzi Noomen Khadija Zouari Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization Case Reports in Surgery |
| 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 |
| url | http://dx.doi.org/10.1155/2021/2868966 |
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