Browse

Secondary Appendiceal Tumors: A Review of 139 Cases

DC Field Value Language
dc.contributor.authorYoon, Won Jae-
dc.contributor.authorYoon, Yong Bum-
dc.contributor.authorKim, Youn Joo-
dc.contributor.authorRyu, Ji Kon-
dc.contributor.authorKim, Yong-Tae-
dc.date.accessioned2012-06-27T06:11:33Z-
dc.date.available2012-06-27T06:11:33Z-
dc.date.issued2010-09-30-
dc.identifier.citationGUT AND LIVER; Vol.4 3; 351-356ko_KR
dc.identifier.issn1976-2283-
dc.identifier.urihttp://hdl.handle.net/10371/77597-
dc.description.abstractBackground/Aims: This study evaluated the clinicopathologic characteristics of patients with secondary appendiceal tumors (SATs). Methods: We performed a single-center, retrospective study of patients with pathologically confirmed SATs. Results: Among 180 cases of appendiceal malignancies diagnosed between 2000 and 2007, 139 cases (77.2%, 46 male) were SATs. The median age at SAT diagnosis was 55 years. The most common primary origin was the ovary. The mode of appendiceal involvement was metastasis in 122 and invasion in 17 patients. Extra-appendiceal involvement was present in 134 patients. The only manifestation that could be attributed to the SAT itself was appendicitis (n=8). Serosal involvement was predominant. The median survival after diagnosis of SAT was 22.6 months. In the Cox regression analysis, chemotherapy included in the treatment was the only factor associated with prolonged survival (hazards ratio, 0.12; 95% confidence interval, 0.06-0.23; p<0.001). Complete resection of the SAT had no influence on survival. Conclusions: SATs accounted for 77.2% of all pathologically diagnosed appendiceal malignancies. The most common origin was the ovary. SATs were usually associated with widespread disease, and the median survival after SAT diagnosis was 22.6 months. Complete resection of the SAT had no influence on survival. (Gut Liver 2010;4:351-356)ko_KR
dc.language.isoenko_KR
dc.publisherEDITORIAL OFFICE GUT & LIVERko_KR
dc.subjectNeoplasmsko_KR
dc.subjectAppendixko_KR
dc.subjectSecondaryko_KR
dc.titleSecondary Appendiceal Tumors: A Review of 139 Casesko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor윤원재-
dc.contributor.AlternativeAuthor윤용범-
dc.contributor.AlternativeAuthor김연주-
dc.contributor.AlternativeAuthor류지곤-
dc.contributor.AlternativeAuthor김용태-
dc.identifier.doi10.5009/gnl.2010.4.3.351-
dc.citation.journaltitleGUT AND LIVER-
dc.description.citedreferenceReddy S, 2008, ANN SURG ONCOL, V15, P3199, DOI 10.1245/s10434-008-0140-7-
dc.description.citedreference*KOR MIN HLTH WELF, 2008, CANC FACTS FIG 2008-
dc.description.citedreferencePIGOLKIN YI, 2008, ARK PATOL, V70, P46-
dc.description.citedreferenceBair MJ, 2007, J FORMOS MED ASSOC, V106, P784-
dc.description.citedreferenceMiller JS, 2006, ARCH PATHOL LAB MED, V130, P407-
dc.description.citedreferenceKloppel G, 2004, ANN NY ACAD SCI, V1014, P13, DOI 10.1196/annals.1294.002-
dc.description.citedreferenceMarsden DE, 2000, SEMIN SURG ONCOL, V19, P11-
dc.description.citedreferenceCARR NJ, 2000, PATHOLOGY GENETICS T, P102-
dc.description.citedreferenceFong Y, 1999, ANN SURG, V230, P309-
dc.description.citedreferenceGopez EV, 1997, AM SURGEON, V63, P778-
dc.description.citedreferenceRose PG, 1997, J SURG ONCOL, V64, P246-
dc.description.citedreferenceBLAIR NP, 1993, AM J SURG, V165, P618-
dc.description.citedreferenceSCHMUTZER KJ, 1975, DIS COLON RECTUM, V18, P324-
dc.description.citedreferenceZELIKOWS.A, 1972, DIS COLON RECTUM, V15, P305-
dc.description.citedreferenceDIETER RA, 1970, DIS COLON RECTUM, V13, P336-
dc.description.tc0-
Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Internal Medicine (내과학전공)Journal Papers (저널논문_내과학전공)
Files in This Item:
There are no files associated with this item.
  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse