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1 ly unimportant lesions (diminutive adenomas, hyperplastic polyps).
2 l polyp were recognized: the adenoma and the hyperplastic polyp.
3 5%) of surgeons recommend surveillance for a hyperplastic polyp.
4 er for sessile serrated adenomas/polyps than hyperplastic polyps.
5 intake on risk of colorectal adenomatous and hyperplastic polyps.
6                          Of the 64, half had hyperplastic polyps.
7 g intake in relation to both adenomatous and hyperplastic polyps.
8 ith an elevated risk of both adenomatous and hyperplastic polyps.
9   An inverse association trend was found for hyperplastic polyps.
10 ll adenoma, and follow-up is not advised for hyperplastic polyps.
11 ng were associated with an increased risk of hyperplastic polyps.
12  1 (5%) of 20 Ashkenazi Jewish patients with hyperplastic polyps.
13          No FDG accumulation was noted in 35 hyperplastic polyps.
14 style factors and the presence of colorectal hyperplastic polyps.
15 ize and was not engendered by nonneoplastic (hyperplastic) polyps.
16  serrated adenomas had a higher frequency of hyperplastic polyps (1.3 +/- 1.6) as compared to patient
17  among patients with no polyps or only small hyperplastic polyps, 132 of 227 (58.1%) with life expect
18 to estimate ORs and 95% CIs among cases (556 hyperplastic polyp, 1753 adenoma, and 208 SSL) and contr
19 ge and sex, was 2.6 for patients with distal hyperplastic polyps, 4.0 for those with distal tubular a
20 nt had no detected lesions, 10.0 percent had hyperplastic polyps, 8.7 percent had tubular adenomas, a
21 nd 1.30 in the 55 cases vs 235 controls with hyperplastic polyps (95% CI, 0.96-1.77).
22 he most advanced lesion present: no polyp, a hyperplastic polyp, a tubular adenoma less than 1 cm in
23 smic staining occurred in about one third of hyperplastic polyps, adenomas, and adenocarcinomas and i
24 carcinoma was compared with classic isolated hyperplastic polyps, adenomas, and solitary serrated ade
25 ide spectrum of intestinal tumors, including hyperplastic polyps, adenomas, small intestinal neuroend
26 adenoma was collected among 81 subjects with hyperplastic polyps and 480 controls.
27 HETE were significantly higher in those with hyperplastic polyps and adenomas compared to those with
28                                              Hyperplastic polyps and fundic gland are the most common
29 nd in excess of guidelines, particularly for hyperplastic polyps and low-risk lesions such as a small
30 nce of endocrine cells compared with classic hyperplastic polyps and normal colon and similar immunoh
31    While HES1 expression is normal in benign hyperplastic polyps and normal colon tissue, HES1 expres
32 tubular and sessile serrated adenomas versus hyperplastic polyps and normal mucosa.
33 sequencing gene expression dataset of benign hyperplastic polyps and potentially malignant sessile se
34 d adenomas (TSAs) are now distinguished from hyperplastic polyps and recognized as precursors to colo
35      The family of serrated lesions includes hyperplastic polyps and sessile serrated adenomas withou
36 ch more similar to serrated adenomas than to hyperplastic polyps and were characterized by large size
37 r gene hMLH1 is diminished or absent in some hyperplastic polyps, and it has been suggested that HPP1
38     No SNP was significantly associated with hyperplastic polyps, and only rs6983267 was significantl
39 those with no polyps, those with one or more hyperplastic polyps, and those with one or more adenomas
40 radic high-grade dysplastic adenomas, and 19 hyperplastic polyps--and tissue derived from patients wi
41   The following factors were associated with hyperplastic polyps: anemia (p = 0.022), single polyp (p
42        Three hundred ninety-one patients had hyperplastic polyps as the worst lesion found at colonos
43 an increased risk of colorectal adenomas and hyperplastic polyps as well as colorectal cancer.
44 ns with no polyps at baseline and those with hyperplastic polyps at baseline (1.1% [12 of 1057] and 2
45                                              Hyperplastic polyps at the initial examination did not p
46  31st 2005, without reported lesions or with hyperplastic polyps, based on secondary data extracted f
47                                    Comparing hyperplastic polyps' biopsies to resected polyps, no dif
48       These serrated polyps include not only hyperplastic polyps but also traditional serrated adenom
49 study were a total of 688 adenoma cases, 210 hyperplastic polyp cases, and 1306 polyp-free controls f
50 ry analysis examined risk factors for having hyperplastic polyps compared with having no polyps and c
51                                            A hyperplastic polyp/dysplasia-to-adenocarcinoma sequence
52 eported that colon carcinomas, adenomas, and hyperplastic polyps exhibiting a serrated histology were
53 he multivariate-adjusted odds ratio (OR) for hyperplastic polyps for individuals in the upper vs. the
54                                      Gastric hyperplastic polyps (GHPs) have a potential risk of neop
55                                              Hyperplastic polyps had a characteristic surface "pit pa
56 VA + VA), sessile serrated adenoma (SSA) and hyperplastic polyp (HP), were assessed (1) for each path
57 regions containing normal epithelium (NE) or hyperplastic polyps (HP) to be distinguished from region
58 ecursors to colorectal cancer (CRC), whereas hyperplastic polyps (HPPs) have low risk of progression
59 444 cases with adenomas only, 662 cases with hyperplastic polyps (HPPs) only, and 437 cases with sync
60 re phosphorylated in serrated areas of human hyperplastic polyps (HPPs), sessile serrated adenomas, a
61 6 of 372) of serrated lesions, respectively; hyperplastic polyps (HPs) accounted for 58.9% (219 of 37
62 s are reported to have multiple and/or large hyperplastic polyps (HPs) and an increased risk of color
63 ts with hyperplastic polyposis have multiple hyperplastic polyps (HPs) and increased risk of colorect
64 l enhancement (M-OE) reliably differentiates hyperplastic polyps (HPs) from other serrated lesions (S
65                           We studied CIMP in hyperplastic polyps (HPs), with emphasis on patients wit
66  lymphoid tissue (MALT) lymphoma, as well as hyperplastic polyps, hyperplastic gastropathy, postendos
67 ty-one percent of respondents would survey a hyperplastic polyp in 5 years or less, 71% would survey
68  and the association between the report of a hyperplastic polyp in the baseline CC report and the pro
69 d be in part attributed to the presence of a hyperplastic polyp in the baseline CC.
70  low risk adenoma in 158 cases (11.3 %), and hyperplastic polyps in 119 cases (8.5 %).
71 lying conditions were hemorrhoids in 7 (6%), hyperplastic polyps in 4 (3.5%), adenomatous polyps in 2
72 patterns appeared: gastric ulcers in 32% and hyperplastic polyps in 68% of gerbils.
73 UFAs were not associated with adenomatous or hyperplastic polyps in either men or women.
74 cid was associated with an increased risk of hyperplastic polyps in men (P-trend = 0.03), which was n
75  comparing serrated polyps with adenomas and hyperplastic polyps in terms of prevalence, morphology,
76 tion between the outcome and the presence of hyperplastic polyps in the baseline CC, showed a statist
77  6 serrated adenomas with multiple (6 to 10) hyperplastic polyps, including 5 with admixed hyperplast
78 stology, they were wild type for BRAF; among hyperplastic polyps, KRAS mutations were found mainly in
79           Despite the high prevalence of the hyperplastic polyp, little is known about its etiology.
80 er in gerbils with ulcers than in those with hyperplastic polyps (median IFN-gamma/glyceraldehyde-3-p
81 that the different outcomes (e.g., ulcers or hyperplastic polyps) might relate to imbalances among cy
82 d be considered a mixed polyp syndrome, with hyperplastic polyps most prevalent, with a risk of early
83 with familial adenomatous polyposis (n = 7), hyperplastic polyps (n = 3), dysplasias arising in ulcer
84    Individuals with SPs were classified into hyperplastic polyps (n = 34; 32%), traditional serrated
85 acent to adenomas or adenocarcinomas (n=41), hyperplastic polyps (n=8), adenomatous polyps (=35), and
86 xclusive categories, including normal colon, hyperplastic polyp, nonadvanced adenoma, and advanced ad
87 mages of neoplastic polyps and 681 images of hyperplastic polyps, obtained from the picture archiving
88 a (odds ratio: 1.60; 95% CI: 1.12, 2.29) and hyperplastic polyps (odds ratio: 1.85; 95% CI: 1.09, 3.1
89 ase of gastric adenocarcinoma arising from a hyperplastic polyp of the fundis of a patient with AAPC.
90 as cloned as a frequently methylated gene in hyperplastic polyps of the colon.
91 fter the following 6 results on colonoscopy: hyperplastic polyp, one 6-mm tubular adenoma, two 6-mm t
92 ases with adenomatous polyps only (n = 639), hyperplastic polyps only (n = 294), and both types of po
93 valuation in 5-10 years, whereas people with hyperplastic polyps only should have a 10-year follow-up
94 for adenoma only, 0.2 (95% CI: 0.1, 0.3) for hyperplastic polyps only, and 0.2 (95% CI: 0.2, 0.4) for
95 tous polyps only, 5.0 (95% CI: 3.3, 7.3) for hyperplastic polyps only, and 6.9 (95% CI: 4.4, 11.1) fo
96 ines, especially if the colonoscopy showed a hyperplastic polyp or a single small adenoma.
97 raphic images and were classified as benign (hyperplastic polyp or regular mucosa) or premalignant (a
98 2% of patients were found to have incidental hyperplastic polyps or adenomas with low-grade dysplasia
99 mas and 34% of adenomatous polyps but not in hyperplastic polyps or normal or transitional mucosa.
100 ory of body mass index had a higher risk for hyperplastic polyps (OR, 4.50; 95% CI, 1.84-10.97).
101   However, failure to recognize adenomas (vs hyperplastic polyps), or discarding a polyp with advance
102  The specificity in individuals with normal, hyperplastic polyps, or nonadvanced adenomas was 82.0% (
103  vary among countries, but SSLs and proximal hyperplastic polyps require special attention in assignm
104                                              Hyperplastic polyps retained this normal compartmentaliz
105 nderestimated precursor lesion, the proximal hyperplastic polyp-serrated adenoma pathway.
106                                 SPs comprise hyperplastic polyps, sessile serrated adenomas/polyps (S
107                                              Hyperplastic polyps share common lifestyle risk factors
108 itivity 0.94; 95% CI 0.90-0.97) and 55 of 62 hyperplastic polyps (specificity 0.89; 0.78-0.95), with
109 s of cigarette smoking and were stronger for hyperplastic polyps than for adenoma.
110 aging system in the identification of distal hyperplastic polyps that do not need resection, as well
111 sh patients with adenomatous polyps, but not hyperplastic polyps.The I1307K mutation represents a nov
112                   Among patients with distal hyperplastic polyps, those with distal tubular adenomas,
113  odds ratios ranged from 1.23 for those with hyperplastic polyps to 1.44 for those with tubulovillous
114 e assigning serrated polyps to categories of hyperplastic polyps, traditional serrated adenomas, and
115 rom normal colonic mucosa, tubular adenomas, hyperplastic polyps, ulcerative colitis, and Crohn's col
116 idual crypts from six colonic adenomas and a hyperplastic polyp were microdissected and characterized
117 ant, adenomatous polyps were present in 25%, hyperplastic polyps were present in 10%, and synchronous
118 ant, adenomatous polyps were present in 16%, hyperplastic polyps were present in 22%, and synchronous
119                                              Hyperplastic polyps were the most common (55.9%), follow
120  the precursor to colorectal cancer, whereas hyperplastic polyps were viewed as innocuous lesions wit
121 st set, the DNN-CAD identified neoplastic or hyperplastic polyps with 96.3% sensitivity, 78.1% specif

 
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