ReviewJournal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract2010
Gastrointestinal and retroperitoneal manifestations of type 1 neurofibromatosis.
Review in Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.
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Who cites it
35 citing papers in PubMed, 79 citations in OpenAlex.
- Type I neurofibromatosis with a solid pseudopapillary neoplasm of the pancreas: a case report and literature review.Discover oncology · 2026Article
- Isolated Anterior Mesenteric Neurofibroma: A Rare Manifestation of Neurofibromatosis Type 1.Cureus · 2026Article
- Isolated Rectal Neurofibroma in the Absence of Neurofibromatosis: Report and Review of Molecular Implications.European journal of case reports in internal medicine · 2026Article
- Mesenteric neurofibromatosis complicated by acute appendicitis: case report and review of the literature.Frontiers in oncology · 2026Article
- Small Intestinal Neurofibroma With Atypical 17q11.2 Microdeletions: A Rare Cause of Abdominal Distension.JGH open : an open access journal of gastroenterology and hepatology · 2025Article
- Article
- Neurofibromatosis Type I Presenting with Incomplete Ileal Volvulus in a Pediatric Patient.The American journal of case reports · 2023Article
- MULTIPLE NEUROENDOCRINE NEOPLASIA IN A PATIENT WITH TYPE I NEUROFIBROMATOSIS (NF1): REPORT OF A NEW MUTATION (NF1, EXONS 2-30 DELETION) AND LITERATURE REVIEW.Arquivos brasileiros de cirurgia digestiva : ABCD = Brazilian archives of digestive surgery · 2023Review
- Reminder for the clinician: abdominal manifestations of type 1 neurofibromatosis are not so uncommon.BMJ case reports · 2022Article
- Challenges in the management of metastatic gastrointestinal stromal tumor in a patient with neurofibromatosis type 1: a case report.Journal of medical case reports · 2022Article
- A case of appendiceal ganglioneuroma in neurofibromatosis type 1.Surgical case reports · 2021Article
- Comprehensive clinicopathologic characteristics of intraabdominal neurogenic tumors: Single institution experience.World journal of clinical cases · 2021Article
- Giant composite pheochromocytoma and gastrointestinal stromal tumor in a patient with neurofibromatosis: A case report.Northern clinics of Istanbul · 2021Article
- Adrenocortical carcinoma in a patient with neurofibromatosis type 1: A case report.Caspian journal of internal medicine · 2021Article
- Abdominal neoplastic manifestations of neurofibromatosis type 1.Neuro-oncology advances · 2020Review
- Multisystem burden of neurofibromatosis 1 in Denmark: registry- and population-based rates of hospitalizations over the life span.Genetics in medicine : official journal of the American College of Medical Genetics · 2020Article
- Isolated colonic neurofibroma, a rare tumor: A case report and review of literature.World journal of clinical cases · 2020Article
- Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966.Orphanet journal of rare diseases · 2020Article
- Recurrent gastrointestinal bleeding in a patient with type 1 neurofibromatosis.BMJ case reports · 2019Article
- A case report of hamartomatous polyposis in an individual with Neurofibromatosis type 1.Clinical case reports · 2019Article
Corrections and comments
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Authors and funding
10 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundType 1 neurofibromatosis (NF1) is a genetic disease characterized by neoplastic and not neoplastic disorders, involving tissues of neuroectodermal or mesenchymal origin. The mainly involved districts are skin, central nervous system, and eye, and there is a wide range of severity of clinical presentations. DATA SOURCES: Abdominal manifestations of NF1 comprehend five categories of tumors: neurogenic with neurofibromas, malignant peripheral nerve sheath tumors and ganglioneuromas, neuroendocrine with pheochromocytomas and carcinoids, non-neurogenic gastrointestinal stromal tumors, i.e., GISTs, and embryonal tumors and miscellaneous.
conclusionsEarly diagnosis of these abdominal manifestations is very important given the risk of malignancy, organic complications such as in the case of pheochromocytomas or hemorrhagic-obstructive complications such as in the case of the tumors of the gastrointestinal tract (GISTs and neurofibromas). The importance of an annual clinical evaluation on the part of a multidisciplinary pool of clinicians in highly specialized centers allows early detection of complications and of neoplastic transformation.
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