Neurofibromatosis Type I and Stromal Tumor with a Multiple Digestive Localization
Autor: | Amina Chaka, Farouk Ennaceur, Mohamed Amine Tormen, Ibtissem Korbi, Faouzi Noomen, Khadija Zouari |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: | |
Zdroj: | Case Reports in Surgery, Vol 2021 (2021) |
Druh dokumentu: | article |
ISSN: | 2090-6900 2090-6919 |
DOI: | 10.1155/2021/2868966 |
Popis: | 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. |
Databáze: | Directory of Open Access Journals |
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