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...
Saved in:
Main Authors: | Amina Chaka, Farouk Ennaceur, Mohamed Amine Tormen, Ibtissem Korbi, Faouzi Noomen, Khadija Zouari |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2021-01-01
|
Series: | Case Reports in Surgery |
Online Access: | http://dx.doi.org/10.1155/2021/2868966 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Retrorectal Schwannomas: Atypical Presentation and Controversial Surgical Management
by: Wided Trimech, et al.
Published: (2021-01-01) -
Malignant Peripheral Nerve Sheath Tumors in Children with Neurofibromatosis Type 1
by: Apostolos Pourtsidis, et al.
Published: (2014-01-01) -
Gastrointestinal stromal tumors
by: A. P. Seryakov
Published: (2010-08-01) -
Achalasia Associated with Neurofibromatosis
by: Stephen N Sullivan
Published: (1991-01-01) -
Using the Neurofibromatosis Tumor Predisposition Syndromes to Understand Normal Nervous System Development
by: Cynthia Garcia, et al.
Published: (2014-01-01)