Carcinoid tumors of the appendix: A population-based study
Background Carcinoid tumors of the appendix are rare, and as such there are few data guiding their optimal treatment. Methods The analysis included all patients with malignant, typical carcinoid tumor of the appendix for whom complete data were available in the Surveillance, Epidemiology, and End Re...
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Published in | Journal of surgical oncology Vol. 104; no. 1; pp. 41 - 44 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.07.2011
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Subjects | |
Online Access | Get full text |
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Summary: | Background
Carcinoid tumors of the appendix are rare, and as such there are few data guiding their optimal treatment.
Methods
The analysis included all patients with malignant, typical carcinoid tumor of the appendix for whom complete data were available in the Surveillance, Epidemiology, and End Results database between 1988 and 2003. Clinicopathologic factors predicting lymph node (LN) involvement and survival were determined.
Results
LN metastases were present in 44 of 89 patients (49%), including 4 of 27 patients (15%) with tumors ≤ 1.0 cm, 16 of 34 patients (47%) with tumors > 1.0 cm but ≤ 2.0 cm, and 24 of 28 patients (86%) with tumors >2.0 cm. Increasing tumor size predicted LN involvement, whereas age, gender, and depth of tumor invasion did not. Excluding patients with distant metastasis (DM), the 10‐year overall survival rates of patients with positive LNs and tumor sizes ≤1.0 cm, >1.0 cm but ≤2.0 cm, and >2.0 cm were 100%, 92%, and 91%, respectively.
Conclusions
Right hemicolectomy should be considered for patients with appendiceal carcinoid tumors >1.0 cm in size given their high incidence of LN metastases and limited data concerning the natural history of unresected LN metastases. J. Surg. Oncol. 2011;104:41–44. © 2011 Wiley‐Liss, Inc. |
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Bibliography: | istex:6D728A9832DB45AB849237FDC64C85664422B39D ArticleID:JSO21888 ark:/67375/WNG-QT4M3HRP-J ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-4790 1096-9098 |
DOI: | 10.1002/jso.21888 |