Background and study aims: The molecular features of serrated polyps (SPs)
with hyperplastic crypt pattern, also called Kudo’s type II observed by
chromoendoscopy, were evaluated.
Methods: The clinicopathological and molecular features of 114 SPs with a
hyperplastic pit pattern detected under chromoendoscopy (five dysplastic SPs, 63
sessile serrated adenoma/polyps (SSA/Ps), 36 microvesicular hyperplastic polyps
(MVHPs), and 10 goblet cell-rich hyperplastic polyps (GCHPs)) were examined. The
frequency of KRAS and BRAF mutations and CpG island methylator
phenotype (CIMP) were investigated.
Results: Dysplastic SPs and SSA/Ps were frequently located in the proximal
colon compared to others (SSA/Ps vs. MVHPs or GCHPs, P < 0.0001). No
significant difference was found in the frequency of BRAF mutation among SPs
apart from GCHP (60 % for dysplastic SPs, 44 % for SSA/Ps, 47 % for MVHPs, and
0 % for GCHPs). The frequency of CIMP was higher in dysplastic SPs or SSA/Ps
than in MVHPs or GCHPs (60 % for dysplastic SPs, 56 % for SSA/Ps, 32 % for
MVHPs, and 10 % for GCHPs) (SSA/Ps vs. GCHP, P = 0.0068). When serrated
neoplasias (SNs) and MVHPs were classified into proximal and distal lesions, the
frequency of CIMP was significantly higher in the proximal compared to the
distal SNs (64 % vs. 11 %, P = 0.0032). Finally, multivariate analysis
showed that proximal location and BRAF mutation were significantly
associated with an increased risk of CIMP.
Conclusions: Distinct molecular features were observed between proximal
and distal SPs with hyperplastic crypt pattern. Proximal MVHPs may develop more
frequently through SSA/Ps to CIMP cancers than distal MVHPs.