Prolapse-related changes are a confounding factor in misdiagnosis of sessile serrated adenomas in the rectum

Summary The differential diagnosis of rectal serrated polyps is challenging due to its unique anatomic location, the evolving concept of serrated polyps over the past several years, and to histologic changes seen in rectal mucosal prolapse. We reclassified 95 rectal polyps diagnosed originally as “s...

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Veröffentlicht in:Human pathology 2013-04, Vol.44 (4), p.480-486
Hauptverfasser: Huang, Cheng Cheng, MD, PhD, Frankel, Wendy L., MD, Doukides, Theodore, MD, Zhou, Xiao-Ping, MD, PhD, Zhao, Weiqiang, MD, PhD, Yearsley, Martha M., MD
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container_end_page 486
container_issue 4
container_start_page 480
container_title Human pathology
container_volume 44
creator Huang, Cheng Cheng, MD, PhD
Frankel, Wendy L., MD
Doukides, Theodore, MD
Zhou, Xiao-Ping, MD, PhD
Zhao, Weiqiang, MD, PhD
Yearsley, Martha M., MD
description Summary The differential diagnosis of rectal serrated polyps is challenging due to its unique anatomic location, the evolving concept of serrated polyps over the past several years, and to histologic changes seen in rectal mucosal prolapse. We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. Thus, histopathologic changes suggesting prolapsed rectal mucosa should take precedence over BRAF results.
doi_str_mv 10.1016/j.humpath.2012.06.011
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We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. 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We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. 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We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. Thus, histopathologic changes suggesting prolapsed rectal mucosa should take precedence over BRAF results.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23069257</pmid><doi>10.1016/j.humpath.2012.06.011</doi><tpages>7</tpages></addata></record>
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subjects Adenoma - diagnosis
Adenoma - epidemiology
Adenoma - genetics
Adult
Aged
Aged, 80 and over
BRAF V600E mutation
Colon
Colonic Polyps - diagnosis
Colonic Polyps - epidemiology
Colonic Polyps - genetics
Colorectal cancer
Comorbidity
Confounding Factors (Epidemiology)
Diagnosis
Diagnosis, Differential
Diagnostic Errors
DNA methylation
DNA Mutational Analysis
DNA, Neoplasm - analysis
Female
Humans
Hyperplasia
Male
Middle Aged
Mutation
Pathology
Proteins
Proto-Oncogene Proteins B-raf - genetics
Rectal Neoplasms - diagnosis
Rectal Neoplasms - epidemiology
Rectal Neoplasms - genetics
Rectal Prolapse - diagnosis
Rectal Prolapse - epidemiology
Rectal Prolapse - genetics
Rectum
Serrated polyp
World Health Organization
title Prolapse-related changes are a confounding factor in misdiagnosis of sessile serrated adenomas in the rectum
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