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Title:Appendiceal neuroendocrine tumors in children and adolescents : the European Cooperative Study Group for Pediatric Rare Tumors (EXPeRT) diagnostic and therapeutic recommendations
Authors:ID Virgone, Calogero (Author)
ID Roganović, Jelena (Author)
ID Rindi, Guido (Author)
ID Kuhlen, Michaela (Author)
ID Jamšek, Jan (Author)
ID Panagopoulou, Paraskevi (Author)
ID Bajčiová, Viera (Author)
ID Ben-Ami, Tal (Author)
ID Raphael, Martine F. (Author)
ID Seitz, Guido (Author), et al.
Files:.pdf PDF - Presentation file, download (682,66 KB)
MD5: 16C01D8D9698A2C48CBBFC9FADB1E842
 
URL URL - Source URL, visit https://www.surgjournal.com/article/S0039-6060(25)00303-4/fulltext
 
Language:English
Typology:1.02 - Review Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Neuroendocrine tumors of the appendix, formerly known as carcinoid tumors, represent a rare entity. They are slow-growing tumors, characterized by an indolent clinical course. In pediatric patients, the 5-year overall survival is estimated to be 100% and the event-free survival slightly less than 100%, with only one reported case of local relapse to date. Nevertheless, a proportion of these patients still undergo a second surgery, mostly represented by right hemicolectomy with mesenteric lymphadenectomy, in consideration of the presence of certain risk factors (size >1.5 or 2 cm; tumors of the appendiceal base with or without suspicious residuals, mesoappendiceal invasion, lymphovascular invasion, serosal breach). This approach represents an overtreatment of patients with a benign clinical course regardless of the presence of risk factors and/or whether a second surgery is performed. National recommendations for diagnosis, treatment, and follow-up of neuroendocrine tumors of the appendix in pediatric age are available in France, Italy, and Germany, but international consensus is lacking. This review presents the internationally harmonized recommendations for the diagnosis and treatment of neuroendocrine tumors of the appendix in children and adolescents, established by the European Cooperative Study Group for Pediatric Rare Tumors group.
Keywords:appendiceal neuroendocrine tumors, pediatric oncology, diagnostic and therapeutic recommendations
Publication status:Published
Publication version:Version of Record
Year of publishing:2025
Number of pages:8 str.
Numbering:Vol. 184, [article no.] 109451
PID:20.500.12556/DiRROS-28839 New window
UDC:616-053.2:616-006
ISSN on article:1532-7361
DOI:10.1016/j.surg.2025.109451 New window
COBISS.SI-ID:274631427 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 9. 4. 2026;
Publication date in DiRROS:09.04.2026
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Downloads:89
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Record is a part of a journal

Title:Surgery
Shortened title:Surgery
Publisher:Mosby
ISSN:1532-7361
COBISS.SI-ID:3618068 New window

Licences

License:CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.

Secondary language

Language:Slovenian
Keywords:apendikularni nevroendokrini tumorji, pediatrična onkologija, diagnostična in terapevtska priporočila


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