Serrated polyposis: rapid and relentless development of colorectal neoplasia
Objective Serrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or adenomas. Although associated with colorectal cancer, the course of SP is not well described. Design 44 patients with SP were studied...
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Published in | Gut Vol. 62; no. 3; pp. 404 - 408 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BMJ Publishing Group Ltd and British Society of Gastroenterology
01.03.2013
BMJ Publishing Group LTD |
Subjects | |
Online Access | Get full text |
ISSN | 0017-5749 1468-3288 1468-3288 |
DOI | 10.1136/gutjnl-2011-300514 |
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Abstract | Objective Serrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or adenomas. Although associated with colorectal cancer, the course of SP is not well described. Design 44 patients with SP were studied. The results of 146 colonoscopies with median follow-up of 2.0 years (range 0–30) and a median of 1.0 years (range 0.5–6) between surveillance colonoscopies were evaluated. Findings from oesophogastroduodenoscopy examinations were analysed. Results The mean age at diagnosis of SP was 52.5±11.9 years (range 22–78). In two pedigrees (5%) another family member had SP. None of 22 patients had gastroduodenal polyps. All patients had additional colorectal polyps at surveillance colonoscopy. SSA/P or adenomas were found in 25 patients (61%) at first colonoscopy and 83% at last colonoscopy. Recurrent SSA/P or adenomas occurred in 68% of patients at surveillance colonoscopy. Three patients had colorectal cancer. Eleven patients (25%) underwent surgery (mean time from diagnosis of SP 2.0±0.9 years). After surgery all seven surveyed patients developed recurrent polyps in the retained colorectum (4/7 had SSA/P or adenomas). No association was found between colorectal neoplasia and sex, age at diagnosis of SP or initial number of colorectal polyps. Conclusions In SP, rapid and unrelenting colorectal neoplasia development continues in the intact colorectum and retained segment after surgery. These findings support the possibility of annual colonoscopic surveillance, consideration for colectomy when SSA/P or adenomas are encountered and frequent postoperative endoscopic surveillance of the retained colorectum. |
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AbstractList | Serrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or adenomas. Although associated with colorectal cancer, the course of SP is not well described.OBJECTIVESerrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or adenomas. Although associated with colorectal cancer, the course of SP is not well described.44 patients with SP were studied. The results of 146 colonoscopies with median follow-up of 2.0 years (range 0-30) and a median of 1.0 years (range 0.5-6) between surveillance colonoscopies were evaluated. Findings from oesophogastroduodenoscopy examinations were analysed.DESIGN44 patients with SP were studied. The results of 146 colonoscopies with median follow-up of 2.0 years (range 0-30) and a median of 1.0 years (range 0.5-6) between surveillance colonoscopies were evaluated. Findings from oesophogastroduodenoscopy examinations were analysed.The mean age at diagnosis of SP was 52.5 ± 11.9 years (range 22-78). In two pedigrees (5%) another family member had SP. None of 22 patients had gastroduodenal polyps. All patients had additional colorectal polyps at surveillance colonoscopy. SSA/P or adenomas were found in 25 patients (61%) at first colonoscopy and 83% at last colonoscopy. Recurrent SSA/P or adenomas occurred in 68% of patients at surveillance colonoscopy. Three patients had colorectal cancer. Eleven patients (25%) underwent surgery (mean time from diagnosis of SP 2.0 ± 0.9 years). After surgery all seven surveyed patients developed recurrent polyps in the retained colorectum (4/7 had SSA/P or adenomas). No association was found between colorectal neoplasia and sex, age at diagnosis of SP or initial number of colorectal polyps.RESULTSThe mean age at diagnosis of SP was 52.5 ± 11.9 years (range 22-78). In two pedigrees (5%) another family member had SP. None of 22 patients had gastroduodenal polyps. All patients had additional colorectal polyps at surveillance colonoscopy. SSA/P or adenomas were found in 25 patients (61%) at first colonoscopy and 83% at last colonoscopy. Recurrent SSA/P or adenomas occurred in 68% of patients at surveillance colonoscopy. Three patients had colorectal cancer. Eleven patients (25%) underwent surgery (mean time from diagnosis of SP 2.0 ± 0.9 years). After surgery all seven surveyed patients developed recurrent polyps in the retained colorectum (4/7 had SSA/P or adenomas). No association was found between colorectal neoplasia and sex, age at diagnosis of SP or initial number of colorectal polyps.In SP, rapid and unrelenting colorectal neoplasia development continues in the intact colorectum and retained segment after surgery. These findings support the possibility of annual colonoscopic surveillance, consideration for colectomy when SSA/P or adenomas are encountered and frequent postoperative endoscopic surveillance of the retained colorectum.CONCLUSIONSIn SP, rapid and unrelenting colorectal neoplasia development continues in the intact colorectum and retained segment after surgery. These findings support the possibility of annual colonoscopic surveillance, consideration for colectomy when SSA/P or adenomas are encountered and frequent postoperative endoscopic surveillance of the retained colorectum. Objective Serrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or adenomas. Although associated with colorectal cancer, the course of SP is not well described. Design 44 patients with SP were studied. The results of 146 colonoscopies with median follow-up of 2.0 years (range 0-30) and a median of 1.0 years (range 0.5-6) between surveillance colonoscopies were evaluated. Findings from oesophogastroduodenoscopy examinations were analysed. Results The mean age at diagnosis of SP was 52.5±11.9 years (range 22-78). In two pedigrees (5%) another family member had SP. None of 22 patients had gastroduodenal polyps. All patients had additional colorectal polyps at surveillance colonoscopy. SSA/P or adenomas were found in 25 patients (61%) at first colonoscopy and 83% at last colonoscopy. Recurrent SSA/P or adenomas occurred in 68% of patients at surveillance colonoscopy. Three patients had colorectal cancer. Eleven patients (25%) underwent surgery (mean time from diagnosis of SP 2.0±0.9 years). After surgery all seven surveyed patients developed recurrent polyps in the retained colorectum (4/7 had SSA/P or adenomas). No association was found between colorectal neoplasia and sex, age at diagnosis of SP or initial number of colorectal polyps. Conclusions In SP, rapid and unrelenting colorectal neoplasia development continues in the intact colorectum and retained segment after surgery. These findings support the possibility of annual colonoscopic surveillance, consideration for colectomy when SSA/P or adenomas are encountered and frequent postoperative endoscopic surveillance of the retained colorectum. Serrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or adenomas. Although associated with colorectal cancer, the course of SP is not well described. 44 patients with SP were studied. The results of 146 colonoscopies with median follow-up of 2.0 years (range 0-30) and a median of 1.0 years (range 0.5-6) between surveillance colonoscopies were evaluated. Findings from oesophogastroduodenoscopy examinations were analysed. The mean age at diagnosis of SP was 52.5 ± 11.9 years (range 22-78). In two pedigrees (5%) another family member had SP. None of 22 patients had gastroduodenal polyps. All patients had additional colorectal polyps at surveillance colonoscopy. SSA/P or adenomas were found in 25 patients (61%) at first colonoscopy and 83% at last colonoscopy. Recurrent SSA/P or adenomas occurred in 68% of patients at surveillance colonoscopy. Three patients had colorectal cancer. Eleven patients (25%) underwent surgery (mean time from diagnosis of SP 2.0 ± 0.9 years). After surgery all seven surveyed patients developed recurrent polyps in the retained colorectum (4/7 had SSA/P or adenomas). No association was found between colorectal neoplasia and sex, age at diagnosis of SP or initial number of colorectal polyps. In SP, rapid and unrelenting colorectal neoplasia development continues in the intact colorectum and retained segment after surgery. These findings support the possibility of annual colonoscopic surveillance, consideration for colectomy when SSA/P or adenomas are encountered and frequent postoperative endoscopic surveillance of the retained colorectum. ObjectiveSerrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or adenomas. Although associated with colorectal cancer, the course of SP is not well described.Design44 patients with SP were studied. The results of 146 colonoscopies with median follow-up of 2.0years (range 0-30) and a median of 1.0years (range 0.5-6) between surveillance colonoscopies were evaluated. Findings from oesophogastroduodenoscopy examinations were analysed.ResultsThe mean age at diagnosis of SP was 52.5 plus or minus 11.9years (range 22-78). In two pedigrees (5%) another family member had SP. None of 22 patients had gastroduodenal polyps. All patients had additional colorectal polyps at surveillance colonoscopy. SSA/P or adenomas were found in 25 patients (61%) at first colonoscopy and 83% at last colonoscopy. Recurrent SSA/P or adenomas occurred in 68% of patients at surveillance colonoscopy. Three patients had colorectal cancer. Eleven patients (25%) underwent surgery (mean time from diagnosis of SP 2.0 plus or minus 0.9years). After surgery all seven surveyed patients developed recurrent polyps in the retained colorectum (4/7 had SSA/P or adenomas). No association was found between colorectal neoplasia and sex, age at diagnosis of SP or initial number of colorectal polyps.ConclusionsIn SP, rapid and unrelenting colorectal neoplasia development continues in the intact colorectum and retained segment after surgery. These findings support the possibility of annual colonoscopic surveillance, consideration for colectomy when SSA/P or adenomas are encountered and frequent postoperative endoscopic surveillance of the retained colorectum. |
Author | Axilbund, Jennifer E Romans, Katharine Edelstein, Daniel L Cruz-Correa, Marcia Giardiello, Francis M Griffin, Constance A Hylind, Linda M |
AuthorAffiliation | 2 Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA 3 Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA 4 Department of Medicine, University of Puerto Rico, San Juan, Puerto Rico 1 Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA |
AuthorAffiliation_xml | – name: 3 Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA – name: 4 Department of Medicine, University of Puerto Rico, San Juan, Puerto Rico – name: 2 Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA – name: 1 Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA |
Author_xml | – sequence: 1 givenname: Daniel L surname: Edelstein fullname: Edelstein, Daniel L email: fgiardi@jhmi.edu organization: Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA – sequence: 2 givenname: Jennifer E surname: Axilbund fullname: Axilbund, Jennifer E email: fgiardi@jhmi.edu organization: Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA – sequence: 3 givenname: Linda M surname: Hylind fullname: Hylind, Linda M email: fgiardi@jhmi.edu organization: Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA – sequence: 4 givenname: Katharine surname: Romans fullname: Romans, Katharine email: fgiardi@jhmi.edu organization: Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA – sequence: 5 givenname: Constance A surname: Griffin fullname: Griffin, Constance A email: fgiardi@jhmi.edu organization: Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA – sequence: 6 givenname: Marcia surname: Cruz-Correa fullname: Cruz-Correa, Marcia email: fgiardi@jhmi.edu organization: Department of Medicine, University of Puerto Rico, San Juan, Puerto Rico – sequence: 7 givenname: Francis M surname: Giardiello fullname: Giardiello, Francis M email: fgiardi@jhmi.edu organization: Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22490521$$D View this record in MEDLINE/PubMed |
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Copyright | Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions Copyright: 2013 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions |
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Snippet | Objective Serrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps... Serrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps (SSA/P) or... ObjectiveSerrated (hyperplastic) polyposis (SP) is a rare disorder with multiple colorectal hyperplastic polyps and often sessile serrated adenomas/polyps... |
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SubjectTerms | Adenoma - diagnosis Adenoma - genetics Adenoma - surgery adenomas Adult Aged Cell Transformation, Neoplastic Cohort Studies Colonic Polyps - pathology Colonic Polyps - surgery Colonoscopy Colorectal cancer colorectal cancer genes colorectal cancer screening colorectal neoplasia colorectal neoplasm Colorectal Neoplasms - diagnosis Colorectal Neoplasms - genetics Colorectal Neoplasms - surgery Endoscopy Endoscopy, Gastrointestinal Family medical history Female Follow-Up Studies Humans Hyperplastic polyps Male Middle Aged Mutation Patients Pedigree Polyps Precancerous Conditions premalignant Recurrence Registries Retrospective Studies sessile serrated adenomas/polyps Statistical analysis Surveillance Tumors Young Adult |
Title | Serrated polyposis: rapid and relentless development of colorectal neoplasia |
URI | http://gut.bmj.com/content/62/3/404.full https://api.istex.fr/ark:/67375/NVC-0B7ZJG89-H/fulltext.pdf https://www.ncbi.nlm.nih.gov/pubmed/22490521 https://www.proquest.com/docview/1779427211 https://www.proquest.com/docview/1284286832 https://www.proquest.com/docview/1753462032 https://pubmed.ncbi.nlm.nih.gov/PMC3963509 |
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