Pathogenesis and Clinical Management of Mesenteric Fibrosis in Small Intestinal Neuroendocine Neoplasms: A Systematic ReviewShow others and affiliations
2020 (English)In: Journal of Clinical Medicine, E-ISSN 2077-0383, Vol. 9, no 6, article id E1777Article, review/survey (Refereed) Published
Abstract [en]
Mesenteric fibrosis (MF) constitutes an underrecognized sequela in patients with small intestinal neuroendocrine neoplasms (SI-NENs), often complicating the disease clinical course. The aim of the present systematic review, carried out by Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) methodology, is to provide an update in evolving aspects of MF pathogenesis and its clinical management in SI-NENs. Complex and dynamic interactions are present in the microenvironment of tumor deposits in the mesentery. Serotonin, as well as the signaling pathways of certain growth factors play a pivotal, yet not fully elucidated role in the pathogenesis of MF. Clinically, MF often results in significant morbidity by causing either acute complications, such as intestinal obstruction and/or acute ischemia or more chronic conditions involving abdominal pain, venous stasis, malabsorption and malnutrition. Surgical resection in patients with locoregional disease only or symptomatic distant stage disease, as well as palliative minimally invasive interventions in advanced inoperable cases seem clinically meaningful, whereas currently available systemic and/or targeted treatments do not unequivocally affect the development of MF in SI-NENs. Increased awareness and improved understanding of the molecular pathogenesis of MF in SI-NENs may provide better diagnostic and predictive tools for its timely recognition and intervention and also facilitates the development of agents targeting MF.
Place, publisher, year, edition, pages
MDPI, 2020. Vol. 9, no 6, article id E1777
Keywords [en]
CTGF, FGF, PDGF, TGF, VEGF, mesenteric fibrosis, neuroendocrine tumors, serotonin, small intestine
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:oru:diva-83195DOI: 10.3390/jcm9061777ISI: 000549312200001PubMedID: 32521677Scopus ID: 2-s2.0-85106714766OAI: oai:DiVA.org:oru-83195DiVA, id: diva2:1441952
Funder
The Royal Swedish Academy of Sciences2020-06-162020-06-162023-12-08Bibliographically approved