Achalasia and squamous cell carcinoma of the esophagus: Analysis of 241 patients
Achalasia of the esophagus is presumed by many to be a premalignant lesion leading to an increased risk of squamous cell carcinoma. There is disagreement, however, as to the precise risk of malignant degeneration and there is no consensus as to either the need for close surveillance of achalasia pat...
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Veröffentlicht in: | The Annals of thoracic surgery 1995-06, Vol.59 (6), p.1604-1609 |
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description | Achalasia of the esophagus is presumed by many to be a premalignant lesion leading to an increased risk of squamous cell carcinoma. There is disagreement, however, as to the precise risk of malignant degeneration and there is no consensus as to either the need for close surveillance of achalasia patients or the surveillance technique that should be employed. A review of the available literature on the subject has disclosed a wide range of reported cancer risks in achalasia patients, from zero to 33 times that of the normal population. Cancers, when discovered, are often unresectable and the median survival when they are resectable is low. A personal experience with 241 achalasia patients treated during the past quarter of a century disclosed that 9 had carcinoma, for a prevalence of 3.7%. Carcinoma developed in 3 of these 9 while they were under our observation. This translates into one cancer per 1,138 patient-years of follow-up, an incidence of 88 per 100,000 population, and a risk 14.5 times that of the age-adjusted and sex-adjusted general population. Because of the low postresection survival rate if treatment is delayed until carcinoma of the esophagus becomes symptomatic, closer surveillance of achalasia patients is recommended than has been the case. Because it seems unlikely that close endoscopic surveillance will prove to be cost-effective, periodic (every 2 to 3 years) blind brush biopsy warrants further study as a means of surveillance. |
doi_str_mv | 10.1016/0003-4975(94)00997-L |
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Henry ; Gibb, S. Peter ; Heatley, Gerald M.</creator><creatorcontrib>Streitz, John M. ; Ellis, F. Henry ; Gibb, S. Peter ; Heatley, Gerald M.</creatorcontrib><description>Achalasia of the esophagus is presumed by many to be a premalignant lesion leading to an increased risk of squamous cell carcinoma. There is disagreement, however, as to the precise risk of malignant degeneration and there is no consensus as to either the need for close surveillance of achalasia patients or the surveillance technique that should be employed. A review of the available literature on the subject has disclosed a wide range of reported cancer risks in achalasia patients, from zero to 33 times that of the normal population. Cancers, when discovered, are often unresectable and the median survival when they are resectable is low. A personal experience with 241 achalasia patients treated during the past quarter of a century disclosed that 9 had carcinoma, for a prevalence of 3.7%. Carcinoma developed in 3 of these 9 while they were under our observation. This translates into one cancer per 1,138 patient-years of follow-up, an incidence of 88 per 100,000 population, and a risk 14.5 times that of the age-adjusted and sex-adjusted general population. Because of the low postresection survival rate if treatment is delayed until carcinoma of the esophagus becomes symptomatic, closer surveillance of achalasia patients is recommended than has been the case. Because it seems unlikely that close endoscopic surveillance will prove to be cost-effective, periodic (every 2 to 3 years) blind brush biopsy warrants further study as a means of surveillance.</description><identifier>ISSN: 0003-4975</identifier><identifier>EISSN: 1552-6259</identifier><identifier>DOI: 10.1016/0003-4975(94)00997-L</identifier><identifier>PMID: 7771859</identifier><identifier>CODEN: ATHSAK</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Carcinoma, Squamous Cell - epidemiology ; Carcinoma, Squamous Cell - etiology ; Carcinoma, Squamous Cell - therapy ; Esophageal Achalasia - complications ; Esophageal Achalasia - pathology ; Esophageal Neoplasms - epidemiology ; Esophageal Neoplasms - etiology ; Esophageal Neoplasms - therapy ; Esophagus ; Female ; Gastroenterology. Liver. Pancreas. 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Henry</creatorcontrib><creatorcontrib>Gibb, S. Peter</creatorcontrib><creatorcontrib>Heatley, Gerald M.</creatorcontrib><title>Achalasia and squamous cell carcinoma of the esophagus: Analysis of 241 patients</title><title>The Annals of thoracic surgery</title><addtitle>Ann Thorac Surg</addtitle><description>Achalasia of the esophagus is presumed by many to be a premalignant lesion leading to an increased risk of squamous cell carcinoma. There is disagreement, however, as to the precise risk of malignant degeneration and there is no consensus as to either the need for close surveillance of achalasia patients or the surveillance technique that should be employed. A review of the available literature on the subject has disclosed a wide range of reported cancer risks in achalasia patients, from zero to 33 times that of the normal population. Cancers, when discovered, are often unresectable and the median survival when they are resectable is low. A personal experience with 241 achalasia patients treated during the past quarter of a century disclosed that 9 had carcinoma, for a prevalence of 3.7%. Carcinoma developed in 3 of these 9 while they were under our observation. This translates into one cancer per 1,138 patient-years of follow-up, an incidence of 88 per 100,000 population, and a risk 14.5 times that of the age-adjusted and sex-adjusted general population. Because of the low postresection survival rate if treatment is delayed until carcinoma of the esophagus becomes symptomatic, closer surveillance of achalasia patients is recommended than has been the case. Because it seems unlikely that close endoscopic surveillance will prove to be cost-effective, periodic (every 2 to 3 years) blind brush biopsy warrants further study as a means of surveillance.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - epidemiology</subject><subject>Carcinoma, Squamous Cell - etiology</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>Esophageal Achalasia - complications</subject><subject>Esophageal Achalasia - pathology</subject><subject>Esophageal Neoplasms - epidemiology</subject><subject>Esophageal Neoplasms - etiology</subject><subject>Esophageal Neoplasms - therapy</subject><subject>Esophagus</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Incidence</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Population Surveillance</subject><subject>Precancerous Conditions - pathology</subject><subject>Prevalence</subject><subject>Risk Factors</subject><subject>Survival Rate</subject><subject>Tumors</subject><issn>0003-4975</issn><issn>1552-6259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rFEEQhpugxE30H0Tog0hyGO3P7WkPwhISFRb0kJyb7p4at2U-Nl0zQv69Pe6yx5yK4n2qqHoIueLsE2d8_ZkxJitljb626oYxa021PSMrrrWo1kLbV2R1Qt6QC8Q_pRUlPifnxhhea7sivzZx5zuPyVM_NBSfZt-PM9IIXUejzzENY-_p2NJpBxRw3O_87xm_0M3gu2dMuERCcbr3U4Jhwrfkdes7hHfHekke7-8ebr9X25_fftxutlVUQkwVqNBoq4RtDQTB6tbaEFhUQdUqSM2M8EwL3q65MVqY0ErRhBqYrAOsLdPyknw87N3n8WkGnFyfcLnaD1AecMZIxqU2BVQHMOYRMUPr9jn1Pj87ztwi0i2W3GLJWeX-i3TbMvb-uH8OPTSnoaO5kn845h6j79rsh5jwhEmtmFSyYF8PGBQXfxNkh7F4itCkDHFyzZhevuMfkQ6NeQ</recordid><startdate>19950601</startdate><enddate>19950601</enddate><creator>Streitz, John M.</creator><creator>Ellis, F. 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Peter ; Heatley, Gerald M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-e4bd59429f7eb208f99bb0c4b484b35072a0521f6177527bf32db8e038be69053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - epidemiology</topic><topic>Carcinoma, Squamous Cell - etiology</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Esophageal Achalasia - complications</topic><topic>Esophageal Achalasia - pathology</topic><topic>Esophageal Neoplasms - epidemiology</topic><topic>Esophageal Neoplasms - etiology</topic><topic>Esophageal Neoplasms - therapy</topic><topic>Esophagus</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Incidence</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Population Surveillance</topic><topic>Precancerous Conditions - pathology</topic><topic>Prevalence</topic><topic>Risk Factors</topic><topic>Survival Rate</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Streitz, John M.</creatorcontrib><creatorcontrib>Ellis, F. Henry</creatorcontrib><creatorcontrib>Gibb, S. 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Peter</au><au>Heatley, Gerald M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Achalasia and squamous cell carcinoma of the esophagus: Analysis of 241 patients</atitle><jtitle>The Annals of thoracic surgery</jtitle><addtitle>Ann Thorac Surg</addtitle><date>1995-06-01</date><risdate>1995</risdate><volume>59</volume><issue>6</issue><spage>1604</spage><epage>1609</epage><pages>1604-1609</pages><issn>0003-4975</issn><eissn>1552-6259</eissn><coden>ATHSAK</coden><abstract>Achalasia of the esophagus is presumed by many to be a premalignant lesion leading to an increased risk of squamous cell carcinoma. There is disagreement, however, as to the precise risk of malignant degeneration and there is no consensus as to either the need for close surveillance of achalasia patients or the surveillance technique that should be employed. A review of the available literature on the subject has disclosed a wide range of reported cancer risks in achalasia patients, from zero to 33 times that of the normal population. Cancers, when discovered, are often unresectable and the median survival when they are resectable is low. A personal experience with 241 achalasia patients treated during the past quarter of a century disclosed that 9 had carcinoma, for a prevalence of 3.7%. Carcinoma developed in 3 of these 9 while they were under our observation. This translates into one cancer per 1,138 patient-years of follow-up, an incidence of 88 per 100,000 population, and a risk 14.5 times that of the age-adjusted and sex-adjusted general population. Because of the low postresection survival rate if treatment is delayed until carcinoma of the esophagus becomes symptomatic, closer surveillance of achalasia patients is recommended than has been the case. 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subjects | Adult Aged Biological and medical sciences Carcinoma, Squamous Cell - epidemiology Carcinoma, Squamous Cell - etiology Carcinoma, Squamous Cell - therapy Esophageal Achalasia - complications Esophageal Achalasia - pathology Esophageal Neoplasms - epidemiology Esophageal Neoplasms - etiology Esophageal Neoplasms - therapy Esophagus Female Gastroenterology. Liver. Pancreas. Abdomen Humans Incidence Male Medical sciences Middle Aged Population Surveillance Precancerous Conditions - pathology Prevalence Risk Factors Survival Rate Tumors |
title | Achalasia and squamous cell carcinoma of the esophagus: Analysis of 241 patients |
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