Endocrine Tumors of the Appendix: A Pathologic Review
* Context.--Although rare, appendiceal endocrine tumors are the most common neoplasms of the appendix. Pathologic analysis is important for guiding themanagement of patients. Objective.--To provide recent data that focus on the pathology of endocrine tumors of the appendix including classifications...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2010-06, Vol.134 (6), p.871-875 |
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container_title | Archives of pathology & laboratory medicine (1976) |
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creator | Deschamps, Lydia Couvelard, Anne |
description | * Context.--Although rare, appendiceal endocrine tumors are the most common neoplasms of the appendix. Pathologic analysis is important for guiding themanagement of patients. Objective.--To provide recent data that focus on the pathology of endocrine tumors of the appendix including classifications and guidelines for patient management. Data Sources.--A review of the recent literature including TNM classifications and patient management guidelines. Conclusions.--Appendiceal endocrine tumors are separated into 2 main groups: classic endocrine tumors and goblet cell carcinoids. They can be classified according to World Health Organization and TNM classifications. Evaluation of their prognoses and risks of malignancy, according to these classifications, depends on several parameters including tumor size, proliferation rate, and infiltration of appendiceal wall and mesoappendix. Most patients with classic endocrine tumors of the appendix have a favorable prognosis. Indications for postappendectomy, complementary surgery, which are still controversial, especially for tumors between 1 and 2 cm, are presented and discussed. In contrast, in patients presenting with a goblet cell carcinoid, a right hemicolectomy after the initial appendectomy is considered the standard surgical intervention. (Arch Pathol Lab Med. 2010;134:871-875) |
doi_str_mv | 10.5858/134.6.871 |
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Pathologic analysis is important for guiding themanagement of patients. Objective.--To provide recent data that focus on the pathology of endocrine tumors of the appendix including classifications and guidelines for patient management. Data Sources.--A review of the recent literature including TNM classifications and patient management guidelines. Conclusions.--Appendiceal endocrine tumors are separated into 2 main groups: classic endocrine tumors and goblet cell carcinoids. They can be classified according to World Health Organization and TNM classifications. Evaluation of their prognoses and risks of malignancy, according to these classifications, depends on several parameters including tumor size, proliferation rate, and infiltration of appendiceal wall and mesoappendix. Most patients with classic endocrine tumors of the appendix have a favorable prognosis. Indications for postappendectomy, complementary surgery, which are still controversial, especially for tumors between 1 and 2 cm, are presented and discussed. In contrast, in patients presenting with a goblet cell carcinoid, a right hemicolectomy after the initial appendectomy is considered the standard surgical intervention. (Arch Pathol Lab Med. 2010;134:871-875)</description><identifier>ISSN: 0003-9985</identifier><identifier>ISSN: 1543-2165</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/134.6.871</identifier><identifier>CODEN: APLMAS</identifier><language>eng</language><publisher>Northfield: College of American Pathologists</publisher><subject>Appendectomy ; Cancer ; Care and treatment ; Classification ; Diagnosis ; Digestive system cancer ; Medical prognosis ; Metastasis ; Neuroendocrine tumors ; Patients ; Practice guidelines (Medicine) ; Prognosis ; Risk factors</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2010-06, Vol.134 (6), p.871-875</ispartof><rights>COPYRIGHT 2010 College of American Pathologists</rights><rights>Copyright College of American Pathologists Jun 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-53d1b49d11ff7bb6fd04cac05296b7df189176da8ef15f375b84e6bd888071d53</citedby><cites>FETCH-LOGICAL-c458t-53d1b49d11ff7bb6fd04cac05296b7df189176da8ef15f375b84e6bd888071d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Deschamps, Lydia</creatorcontrib><creatorcontrib>Couvelard, Anne</creatorcontrib><title>Endocrine Tumors of the Appendix: A Pathologic Review</title><title>Archives of pathology & laboratory medicine (1976)</title><description>* Context.--Although rare, appendiceal endocrine tumors are the most common neoplasms of the appendix. Pathologic analysis is important for guiding themanagement of patients. Objective.--To provide recent data that focus on the pathology of endocrine tumors of the appendix including classifications and guidelines for patient management. Data Sources.--A review of the recent literature including TNM classifications and patient management guidelines. Conclusions.--Appendiceal endocrine tumors are separated into 2 main groups: classic endocrine tumors and goblet cell carcinoids. They can be classified according to World Health Organization and TNM classifications. Evaluation of their prognoses and risks of malignancy, according to these classifications, depends on several parameters including tumor size, proliferation rate, and infiltration of appendiceal wall and mesoappendix. Most patients with classic endocrine tumors of the appendix have a favorable prognosis. Indications for postappendectomy, complementary surgery, which are still controversial, especially for tumors between 1 and 2 cm, are presented and discussed. In contrast, in patients presenting with a goblet cell carcinoid, a right hemicolectomy after the initial appendectomy is considered the standard surgical intervention. 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Couvelard, Anne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-53d1b49d11ff7bb6fd04cac05296b7df189176da8ef15f375b84e6bd888071d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Appendectomy</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Classification</topic><topic>Diagnosis</topic><topic>Digestive system cancer</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Neuroendocrine tumors</topic><topic>Patients</topic><topic>Practice guidelines (Medicine)</topic><topic>Prognosis</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deschamps, Lydia</creatorcontrib><creatorcontrib>Couvelard, Anne</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deschamps, Lydia</au><au>Couvelard, Anne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endocrine Tumors of the Appendix: A Pathologic Review</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><date>2010-06-01</date><risdate>2010</risdate><volume>134</volume><issue>6</issue><spage>871</spage><epage>875</epage><pages>871-875</pages><issn>0003-9985</issn><issn>1543-2165</issn><eissn>1543-2165</eissn><coden>APLMAS</coden><abstract>* Context.--Although rare, appendiceal endocrine tumors are the most common neoplasms of the appendix. Pathologic analysis is important for guiding themanagement of patients. Objective.--To provide recent data that focus on the pathology of endocrine tumors of the appendix including classifications and guidelines for patient management. Data Sources.--A review of the recent literature including TNM classifications and patient management guidelines. Conclusions.--Appendiceal endocrine tumors are separated into 2 main groups: classic endocrine tumors and goblet cell carcinoids. They can be classified according to World Health Organization and TNM classifications. Evaluation of their prognoses and risks of malignancy, according to these classifications, depends on several parameters including tumor size, proliferation rate, and infiltration of appendiceal wall and mesoappendix. Most patients with classic endocrine tumors of the appendix have a favorable prognosis. Indications for postappendectomy, complementary surgery, which are still controversial, especially for tumors between 1 and 2 cm, are presented and discussed. In contrast, in patients presenting with a goblet cell carcinoid, a right hemicolectomy after the initial appendectomy is considered the standard surgical intervention. (Arch Pathol Lab Med. 2010;134:871-875)</abstract><cop>Northfield</cop><pub>College of American Pathologists</pub><doi>10.5858/134.6.871</doi><tpages>5</tpages></addata></record> |
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source | Allen Press Journals; EZB-FREE-00999 freely available EZB journals |
subjects | Appendectomy Cancer Care and treatment Classification Diagnosis Digestive system cancer Medical prognosis Metastasis Neuroendocrine tumors Patients Practice guidelines (Medicine) Prognosis Risk factors |
title | Endocrine Tumors of the Appendix: A Pathologic Review |
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