Evidence map›Paper›PMID 41808599›Full record

ArticleTurk patoloji dergisi2026

Histopathological and Molecular Features of Adenomatous and Serrated Colon Adenomas, Characteristics and Overlapping Features, Challenges in the Nomenclature.

Buket Bambul Sigirci, Ismail Yilmaz, Sibel Erdamar Çetin, Enver Yarikkaya, Merve Cin, Esra Pasaoglu, Nevra Dursun

Abstract read
In one paragraph

Article in Turk patoloji dergisi, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Buket Bambul SigirciDepartment of Pathology, Sisli Hamidiye Etfal Training and Research Hospital, İSTANBUL, TÜRKİYE.
Ismail YilmazDepartment of Pathology, Sultan Abdulhamid Han Training and Research Hospital, İSTANBUL, TÜRKİYE.
Sibel Erdamar ÇetinDepartment of Pathology, Ac�±badem University, İSTANBUL, TÜRKİYE.
Enver YarikkayaDepartment of Pathology, Istanbul Training and Research Hospital, İSTANBUL, TÜRKİYE.
Merve CinDepartment of Pathology, Istanbul Training and Research Hospital, İSTANBUL, TÜRKİYE.
Esra Pasaoglu
Nevra DursunDepartment of Pathology, Basaksehir Cam ve Sakura City Hospital, İSTANBUL, TÜRKİYE.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveColorectal cancer develops from precursor epithelial polyps, including tubular adenomas, villous or tubulovillous adenomas, sessile serrated lesions, and traditional serrated adenomas. Although diagnostic criteria for these lesions have been established, overlapping features often complicate classification. This study aimed to define the characteristics and shared features of colorectal adenomas. MATERIAL AND

methodsA total of 140 adenomas were evaluated, comprising 71 conventional adenomas, 34 sessile serrated lesions, and 35 traditional serrated adenomas. Hematoxylin and eosin-stained slides were reviewed. Macroscopic features, including sessile or polypoid structure, were documented from pathology and endoscopy reports. Histopathological features were assessed first as present or absent, and then by extent using a four-tiered scale (0: less than 10%, 1: 10-25%, 2: 25-75%, 3: more than 75%). Sixteen adenomas with overlapping features were classified as hybrid or unclassified. Molecular studies, including mutation analysis of KRAS, NRAS, and BRAF, as well as microsatellite instability and MLH1 promoter methylation, were performed in 50 cases.

resultsNo gender predominance was identified. Sessile morphology was most common in sessile serrated lesions and hybrid adenomas. Conventional adenomas showed serration in 50% of cases and ectopic crypts in 23%, though usually involving less than 25% of the lesion. Adenomatous dysplasia was present in most traditional serrated adenomas and nearly half of sessile serrated lesions, while serrated dysplasia occurred in a minority of conventional adenomas. KRAS mutations predominated in conventional (55%) and hybrid adenomas (80%), whereas BRAF mutations were most frequent in sessile serrated lesions (60%) and traditional serrated adenomas (40%); MLH1 promoter methylation was observed across all types, while no NRAS mutations or microsatellite instability were detected.

conclusionHistopathological features overlapped among all adenoma types, and no single feature was lesion-specific. Applying quantitative thresholds may improve diagnostic accuracy and reduce interobserver variability.

Indexed as

AdenomaColonic NeoplasmsColonic PolypsColorectal NeoplasmsTerminology as TopicAdultAgedAged, 80 and overDNA Mutational AnalysisFemaleHumansMaleMembrane ProteinsMicrosatellite InstabilityMiddle AgedMutationBRAF protein, humanKRAS protein, humanMembrane ProteinsMLH1 protein, humanMutL Protein Homolog 1Proto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)

Identifiers

PMID41808599
PMCPMC13600671

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.