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Original article 81

Some diminutive colorectal polyps can be removed


and discarded without pathological examination

Authors B. Denis1,2, J. Bottlaender1, A. M. Weiss1, A. Peter1, G. Breysacher1, P. Chiappa1, P. Perrin2

1
Institutions Médecine A, Hôpital Pasteur, Colmar, France
2
ADECA Alsace, Colmar, France

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submitted Background and study aims: Pathological exam- minutive polyps either associated with a cancer
15 September 2009 ination of colorectal polyps is useful if clinical or a polyp measuring ≥ 10 mm or removed in
accepted after revision management is affected (i. e. when invasive carci- very old or frail patients could be omitted without
28 September 2010
noma is detected or postpolypectomy surveil- any consequence for the patient. If diminutive
Bibliography lance interval is guided). Our aim was to assess polyps one or two in number were discarded
DOI http://dx.doi.org/ whether the pathological examination of some without pathological examination in patients
10.1055/s-0030-1255952 diminutive (measuring ≤ 5 mm) polyps can be with a personal history of colorectal neoplasm,
Published online omitted. three patients out of 43 would have a 5-year in-
24 November 2010
Patients and methods: Consecutive patients un- stead of a 3-year surveillance interval. As a whole,
Endoscopy 2011; 43:
81–86 © Georg Thieme
dergoing a colonoscopy at Pasteur Hospital (Col- if 44.1 % (95 % CI 38.0 – 50.1) of diminutive polyps
Verlag KG Stuttgart · New York mar, France) between January and August 2008 were discarded, the surveillance interval would
ISSN 0013-726X were included in this prospective study. Six senior remain identical in 98.3 % (95 % CI 96.4 – 100) of
gastroenterologists predicted the future surveil- patients.
Corresponding author
lance interval without referring to the result of Conclusions: The pathological examination of up
B. Denis, MD
Médecine A pathological examination. to 44 % of diminutive polyps (i. e. 33 % of all
Hôpital Pasteur Results: In all, 350 polyps from 175 patients polyps), can be safely omitted. The pathological
39 avenue de la Liberté were removed and analyzed. The endoscopist examination would be required only for those
68024 Colmar was able to predict the correct surveillance inter- with suspicious gross appearance, those three or
France val without referring to the result of pathological more in number, and those isolated one or two
Fax: +33-3-89124533
examination in 118 patients (67.4 %; 95 % confi- in number that are removed from people without
bernard.denis@ch-colmar.fr
dence interval [CI] 60.5 – 74.4). The pathological personal history of colorectal neoplasm.
examination of 18.4 % (95 % CI 13.7 – 23.1) of di-

Introduction sis. The pathological examination however is of


! value only if clinical management is affected (i. e.
Colorectal cancer (CRC) can be prevented by re- when invasive carcinoma is detected or when the
moving colorectal neoplasia. Several studies have postpolypectomy surveillance interval is guided).
demonstrated that CRC incidence is reduced after Moreover it places a huge burden on pathologists
polypectomy [1 – 3]. After polypectomy, decisions and its cost is not negligible, even though it is nota-
regarding surveillance intervals are based on pa- bly lower than that of the colonoscopy itself. Some
thology findings of the removed specimens. For authors have suggested that the pathological ex-
example, colonoscopic surveillance is required amination of some small (6 – 9 mm) and/or di-
when polyps are adenomatous but generally not minutive (≤ 5 mm) polyps could be omitted [4 –
when they are nonadenomatous. A 3-year surveil- 7]. For example, Külling et al. found that the patho-
lance interval is warranted for advanced adeno- logical examination of a right-sided diminutive
mas, whereas a 5-year interval is recommended polyp in a patient < 60 years might not always be
for nonadvanced adenomas. Decisions regarding necessary because it was associated with a low
surgical resection after endoscopic removal of ma- risk (3.8 %) of advanced pathologic features [4].
lignant polyps are based on pathological features The aim of our study was to ascertain whether the
and adequacy of endoscopic resection. It is usually pathological examination of some diminutive
recommended that every effort should be made to polyps could be omitted without undue risk to
retrieve all resected tissue for pathological analy- the patient.

Denis B et al. Pathological examination of diminutive polyps … Endoscopy 2011; 43: 81 – 86


82 Original article

Groups of patients Number Total number Number Table 1 Distribution


of DPs, (%) of polyps of patients of diminutive polyps.

No DP 0 (0) 43 32
Any DP in very old or frail patient 7 (2.7) 7 4
Any DP associated with cancer or polyp(s) ≥ 10 mm 41 (15.7) 71 27
Any DP among three or more polyps < 10 mm 106 (40.6) 116 32
Any DP among two or less polyps < 10 mm
One DP associated with one polyp 6 – 9 mm 6 (2.3) 12 6
One or two DPs isolated with history* 61 (23.4) 61 43
One or two DPs isolated without history* 40 (15.3) 40 31
Total 261 (100) 350 175
DP: diminutive polyp. History*: personal history of colorectal neoplasm.

Patients and methods


Discard without

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! Pathological examination
pathological examination
All colonoscopic procedures performed between January and Au-
gust 2008 in the endoscopy unit of the Pasteur Hospital in Colmar
were prospectively recorded. They were performed by six senior Polyps

gastroenterologists. The endoscopist completed a form for each


Polyps > 5 mm
colonoscopy that displayed polyp(s) and specified before the pro-
cedure whether the colonoscopic procedure was the first for the
patient, whether there was a history of CRC or adenoma, and Polyps ≤ 5 mm
whether there was a first-degree family history of CRC. People
with a history of inflammatory bowel disease, of adenomatous Suspicious gross
polyposis coli or of hereditary nonpolyposis colorectal cancer Very old or
appearance
were excluded. At the end of the procedure, the endoscopist reg- frail people
istered the details of all polyps removed: number, shape, loca-
tion, and size. The polyp size was measured in vitro with a ruler Associated with cancer
in the endoscopy suite immediately after retrieval and before or polyp(s) ≥ 10 mm
3 or more polyps
fixation. Finally, the endoscopist specified whether or not colo- < 10 mm
noscopic surveillance was necessary, the proposed surveillance 1 polyp ≤ 5 mm associated
interval, and the reason(s) for the proposed surveillance. with 1 polyp 6–9 mm
The pathological examination of polyps was performed as usual
1 or 2 polyps
by four senior general pathologists. After the pathological exam- ≤ 5 mm
ination, the endoscopist completed the form with the details of
each polyp (histological type and degree of dysplasia) and speci-
History* no history*
fied the final surveillance interval recommended when taking
into account the results of the pathological examination. Finally,
the endoscopist specified the number of polyps for which the
pathological examination had been useful. Fig. 1 Proposed algorithm for the management of polyps.
The surveillance intervals after polypectomy described in the *History refers to personal history of colorectal neoplasm.
French guidelines [8] were considered appropriate: briefly, a
3-year interval was recommended for patients with any advanced
adenoma, three or more adenomas or any adenoma and a family and villous (> 80 %). Serrated polyps were classified as hyperplas-
history of CRC; a 5-year interval was recommended in all other pa- tic polyp or serrated adenoma (including sessile serrated adeno-
tients with adenoma, either classical or serrated. ma, traditional serrated adenoma, and mixed serrated polyp) ac-
cording to the terminology published in the review of Snover et
Classification of diminutive polyps al. [10]. Dysplasia was classified according to the revised Vienna
The diminutive polyps were classified into different groups tak- classification of gastrointestinal epithelial neoplasia [11, 12]. In
ing into account the criteria used for the determination of the situ and intramucosal carcinomas (categories 4.2 and 4.4 in the
surveillance intervals (● " Table 1; ●
" Fig. 1). Very old or frail pa- revised Vienna classification and Tis in the tumor-node-metasta-
tients included persons with advanced age or co-morbidities sis [TNM] classification) were classified as high grade neoplasia
leading to < 10 years’ life expectancy according to the judgement [11 – 13]. Cancer was defined as carcinoma invading at least the
of the endoscopist. submucosa across the muscularis mucosae (category 5 in the re-
vised Vienna classification) [11, 12]. Advanced adenoma was de-
Pathological classification fined as an adenoma measuring ≥ 10 mm or with a villous com-
Polyps were classified as hyperplastic polyps or adenomas ac- ponent > 20 % or with high grade dysplasia or invasive carcinoma.
cording to the World Health Organization classification [9]. Ade-
nomas were further classified as serrated or classical. According
to percentage of villous elements, classical adenomas were classi-
fied as tubular (< 20 % villous elements), tubulovillous (20 – 80 %),

Denis B et al. Pathological examination of diminutive polyps … Endoscopy 2011; 43: 81 – 86


Original article 83

Statistical methods
Table 2 Distribution of polyps according to size.
The chi-squared test was used to test for statistical significance by
comparison of proportions. The significance threshold was set at Polyp type Polyp size All
0.05.
≤ 5 mm 6 – 9 mm ≥ 10 mm
Number, 261 (74.6) 35 (10.0) 54 (15.4) 350 (100)
n (%)
Results
Adenoma- 180 (69.0) 29 (82.9) 51 (94.4) 260 (74.3)
!
tous polyp,
A total of 355 polyps were removed during 175 colonoscopic pro- n (%)*
cedures in 68 women and 107 men with a mean age of 64.8 years Advanced 22 (12.2) 13 (44.8) 51 (100) 86 (33.1)
(range 36 – 86 years). Among the colonoscopies, 47.4 % were a adenoma,
first procedure and 46.5 % a surveillance procedure after polypec- n (%) †
tomy or surgery for CRC. A first-degree family history of CRC was Invasive 0 (0) 0 (0) 2 (3.9) 2 (0.8)
carcinoma,
present in 13.9 % of cases. The pathological examination had not
n (%) †
been performed in five polyps, leaving 350 polyps to be assessed.
*As % of polyps. †As % of adenomas.
Their distribution according to size is presented in ●

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" Table 2. In

all, 261 diminutive polyps were removed in 143 people. They


accounted for 74.6 % of the polyps. Of these, 15.7 % were associat-
ed with either a CRC or a polyp ≥ 10 mm in size and 38.7 % were If the 48 diminutive polyps that were either associated with a
isolated one or two in number (● " Table 1). There was no invasive CRC or a polyp ≥ 10 mm in size or removed in very old or frail pa-
carcinoma among them and 22 (12.2 %) were advanced adeno- tients had been discarded without pathological examination, the
mas: 11 displayed high grade dysplasia, nine villous features, surveillance interval would have remained correct in all these 31
and two both. patients (●" Table 3). If the six diminutive polyps that were asso-

The pathological examination was estimated to be useful by the ciated with a polyp 6 – 9 mm in size had been discarded, the sur-
endoscopist for 146 polyps (41.7 %). This rate of useful examina- veillance interval would have remained correct in all six patients.
tions varied according to the size of polyp (26.1 % for polyps If the 61 diminutive polyps that were isolated one or two in num-
measuring ≤ 5 mm, 80.0 % for 6 – 9 mm, and 92.6 % for ≥ 10 mm; ber had been discarded in patients with a personal history of
P < 0.001) and the context (53.6 % in case of a first procedure and colorectal neoplasm, three of 43 patients would have had a sur-
29.8 % in case of a surveillance procedure; P < 0.001). At the end of veillance interval of 5 years instead of 3 years. Overall, depending
the colonoscopy, the endoscopist could specify for 133 patients on the kind of diminutive polyps discarded without pathological
(76.0 %) whether or not colonoscopic surveillance was necessary examination, their number would vary from 18.4 % (95 % CI 13.7 –
and propose a surveillance interval. This rate varied from 60.0 % 23.1) to 44.1 % (95 % CI 38.0 – 50.1), and the related rate of correct
in 65 patients without family history of CRC having a first proce- surveillance intervals in the whole cohort would vary respective-
dure, to 91.2 % in 80 patients having a surveillance procedure for ly from 100 % to 98.3 % (172/175; 95 % CI 96.4 – 100) for both
CRC or adenoma. The surveillance proposed by the endoscopist French and US guidelines (● " Table 3). If a 3-year surveillance in-

was confirmed by the result of pathological examination in 118 terval had been proposed for the 32 patients with three or more
patients (88.7 %) and modified in 15 patients (11.3 %): the surveil- polyps measuring < 10 mm without pathological examination of
lance interval was shortened in 11 cases, lengthened in two, and diminutive polyps, surveillance would have been either too early
the surveillance was cancelled in two cases. As a whole, the en- or unnecessary in 19 patients (59.4 %).
doscopist was able to predict the correct surveillance interval Using the French pathology fees, the total cost for histopathology
without the result of pathological examination in 118 patients for 175 patients was € 10 192. Depending on the kind of diminu-
(67.4 %) (95 % CI 60.5 – 74.4). This rate was respectively 50.8 % in tive polyps discarded without pathological examination, the cost
patients without family history of CRC having a first procedure reduction would vary from € 1058 to € 3511 (10.4 % to 34.5 %)
and 82.5 % in patients having a surveillance procedure. (●" Table 3).

Diminutive polyps Number Number of patients with Savings, € Table 3 Accuracy of the sur-
discarded without of polyps (%) correct surveillance interval/ veillance intervals determined
without pathological examina-
pathological examination number of patients (%)
tion of some diminutive polyps,
[95 % CI] [95 % CI]
and generated savings in re-
Any number associated with cancer 48 (18.4) 31/31 (100) 1058.4 duced pathology costs (accord-
or polyp(s) ≥ 10 mm [13.7 – 23.1] [100 – 100] ing to French and US guide-
or in very old or frail patient lines).
One associated with a polyp 6 – 9 mm 6 (2.3) 6/6 (100) 252.0
[0.5 – 4.1] [100 – 100]
One or two isolated with history* 61 (23.4) 40/43 (93.0) 2200.8
[18.2 – 28.5] [85.4 – 100]
Total 115 (44.1) 77/80 (96.3) 3511.2
[38.0 – 50.1] [92.1 – 100]
*Personal history of colorectal neoplasm.

Denis B et al. Pathological examination of diminutive polyps … Endoscopy 2011; 43: 81 – 86


84 Original article

Discussion
Table 4 Rate of invasive carcinoma within diminutive adenomas.
!
Our study suggests that the pathological examination of some di- Author [ref.] Number of Carcinoma,
minutive polyps can be safely omitted. Their number varies from diminutive n (%)
18 % to 44 % depending on the level of risk one accepts for the sur- adenomas
veillance interval. The pathological examination of diminutive Matek et al. 1985 [17] 2214 0 (0)
polyps that are either associated with a CRC or a polyp ≥ 10 mm Weston & Campbell 1995 [18] 919 0 (0)
in size or removed in very old or frail people (i. e. 18 % of them), Nusko et al. 1997 [16] 5027 0 (0)
can be omitted without any risk. If those associated with a polyp Gschwantler et al. 2002 [19] 3016 0 (0)
6 – 9 mm in size were discarded (i. e. 2 % of them), the surveillance Church 2004 [20] 2066 2 (0.1)
interval would remain correct in all six patients. If those isolated Odom et al. 2005 [5] 2851 1 (0.03)
one or two in number were discarded in people having a perso- Butterly et al. 2006 [21] 1305 1 (0.08)
Yoo et al. 2007 [22] 3303 1 (0.03)
nal history of colorectal neoplasm (i. e. 23 % of them), three of 43
Lieberman et al. 2008 [23] 3744 1 (0.03)
patients would have a 5-year surveillance interval instead of a 3-
Rex et al. 2009 [24] 4326 4 (0.09)
year interval. This rate of misclassification seems minor and
Total 28 771 10 (0.03)

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acceptable in current practice.
The benefit of not examining diminutive polyps is a cost reduc-
tion, but what are the actual risks of such a policy? After polypec-
tomy, the endoscopist has two questions to answer: 1) Is there associated with either a CRC or a polyp measuring ≥ 10 mm be-
any invasive carcinoma and, if yes, what is the appropriate treat- cause whatever their histology, the surveillance interval will be
ment? 2) Is surveillance necessary and, if yes, what is the appro- 3 years. Likewise, it has strictly no impact in those removed in
priate surveillance interval? very old or frail people as there is no need for surveillance what-
The pathologist is indispensable in answering the first question. ever the diminutive polyp histology. Moreover, it has only a
The pathologist has to determine whether the submucosa has minute impact on the management in those isolated one or two
been invaded and assess the prognostic factors that determine in number that are removed in people having a personal history
whether polypectomy is sufficient or whether a colectomy would of colorectal neoplasm, as they will need a surveillance colonos-
be necessary. The risk of invasive carcinoma is related to the ade- copy at least every 5 – 10 years whatever the kind of polyp re-
noma size [14 – 16] and can be considered as negligible within di- moved [8, 29]. Our results are somewhat lower than those ob-
minutive adenomas. It varies between 0 [16 – 19] and 0.1 % [20] in tained with narrow-band imaging: we could predict a surveil-
the literature and is estimated at 0.03 % when pooling the largest lance interval without pathological examination of diminutive
published series [5, 16 – 24] (● " Table 4). Moreover, these very polyps in 45.7 % (80 of 175) of our patients, which was correct in
small carcinomas should be generally recognized by the endos- 96 % (77 of 80) of cases (●
" Table 3), whereas Ignjatovic et al. could

copist on their macroscopic features, as they almost invariably oc- predict in 63.1 % (82 of 130) of their patients, correct in 95 – 98 %
cur in lesions with a depressed morphology [25]. of cases [27]. The two approaches might however be complemen-
To determine the postpolypectomy surveillance interval, the en- tary, the endoscopic characterization being particularly useful for
doscopist has two questions to answer: 1) Is surveillance neces- diminutive polyps three or more in number, those isolated one or
sary (or is the polyp neoplastic), and if it is 2) What is the appro- two in number in people without history of colorectal neoplasm,
priate surveillance interval (or is the adenoma advanced)? Cur- and for small polyps. Both approaches however share the same
rently, the pathological examination is the “gold standard” for drawback as they do not take into account advanced pathological
distinguishing between adenomatous polyps that require colo- features.
noscopic surveillance and nonadenomatous polyps, which usual- We believe, with others, that the role attributed today to the pa-
ly do not. Using conventional endoscopy, the endoscopist is not thology results for distinguishing between a 3- and a 5-year sur-
accurate enough to differentiate a hyperplastic from an adeno- veillance interval is excessive and should be reduced [30 – 32]. As
matous polyp [26, 27]. By contrast, imaging technologies such as there is no standard definition of villous architecture and high
optical magnification, chromoendoscopy, narrow-band imaging, grade dysplasia and considering the lack of reproducibility, the
confocal endomicroscopy, and autofluorescence imaging en- length of surveillance interval cannot reliably depend on these
hance the accuracy of the endoscopist. Some authors have pro- pathological features [30 – 32]. The accuracy of pathologists for
posed to replace the pathological examination by in vivo charac- the diagnosis of villous histology and high grade dysplasia is
terization between neoplastic and non-neoplastic polyps using poor-to-moderate, so that, in our opinion, these advanced patho-
these techniques. In this way only suspected invasive lesions are logical features should be abandoned for clinical use [32 – 38].
sent for pathological examination, whereas nondepressed polyps The definition of the advanced adenoma should be simplified
<10 mm in size could be left in situ if non-neoplastic, or resected and restricted to adenomas measuring ≥ 10 mm. It should be pos-
and disposed of if assessed as adenomatous, without the need for sible in most cases to determine the surveillance interval with
formal histology [6, 7, 27]. However, the accuracy of these tech- only clinical and macroscopic criteria such as polyp size and
niques is far from 100 % and most of them are expensive, increase number, these criteria being those most strongly correlated with
the colonoscopic procedure time, require special training, have advanced adenoma recurrence [29, 39, 40]. Guidelines remain to
been assessed in expert hands only, and have yet to be compared be elaborated. They should be close to the British guidelines,
one with another [28]. which do not take into account advanced pathological features
Our approach is different and original. It is mainly founded on the in adenomas ≤ 10 mm in size for the determination of the surveil-
fact that the discrimination between neoplastic and non-neo- lance interval [41]. In our study, the endoscopist was able to pre-
plastic polyps, either by the pathologist or by the endoscopist, dict the correct surveillance interval at the end of the colonosco-
has strictly no impact on the management in diminutive polyps py in 67.4 % of cases, without the results of pathological examina-

Denis B et al. Pathological examination of diminutive polyps … Endoscopy 2011; 43: 81 – 86


Original article 85

tion. This rate was even higher at 82.5 % in people with a personal interval is enough, as recommended by British guidelines [41].
or a family history of colorectal neoplasm. Besides, we propose There is no evidence that an isolated adenoma measuring
another original approach mainly founded on the fact that ad- < 10 mm with villous features or high grade dysplasia requires 3-
vanced histology is related to polyp size [14, 19, 21 – 23]. We pro- year instead of 5-year surveillance [30, 31, 45].
pose to remove and discard the smallest polyp(s) that are asso- Another question remains unanswered: What should we do with
ciated with a larger polyp. This approach relies on the hypothesis diminutive polyps detected on colonoscopy? To date it is usually
that the histology of the largest polyp is more advanced than that recommended to report, remove, and analyze all raised mucosal
of smaller polyp(s). This was true in all six patients with a di- colorectal lesions irrespective of size and appearance. This cur-
minutive polyp associated with a small polyp and, of course, in rently accepted practice will probably have to change in the set-
all 33 patients with diminutive polyp(s) associated with large ting of mass CRC screening as it is expensive and has a low level of
polyp(s). The risk of misclassification was thus negligible (mark- evidence if the goal of colonoscopy is cancer prevention. All in all,
edly lower than that obtained by pathologists when assessing vil- the same arguments that lead radiologists to ignore diminutive
lous histology and high grade dysplasia), and considered accept- polyps detected on computed tomographic colonography can be
able [32 – 38]. used to omit the pathological examination of those removed dur-
Our study underlines the importance of measuring the polyp ing colonoscopy [45, 46]. Many experienced endoscopists simi-

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size. Two size cut-offs are clinically important: 5 mm because larly do not report distal diminutive polyps that they consider to
polyps measuring > 5 mm will need pathological examination be hyperplastic, and instead leave them in situ provided a sur-
whereas some of those ≤ 5 mm in size will not, and 10 mm be- veillance colonoscopy is planned. Our study suggests that all di-
cause polyps ≥ 10 mm will need a 3-year surveillance colonosco- minutive polyps should be removed because of the non-negligi-
py. As in vivo measurement of polyp size is not accurate enough, ble risk of advanced adenoma. In all, 12.2 % of our diminutive ade-
we measure it with a ruler in vitro immediately after retrieval nomas were advanced, which is by far higher than the range of
[42]. This measurement is easy and quick to perform and should 0.2 – 8.5 % reported in previous studies [4, 20 – 24]. The high CRC
be done in current practice, especially for sizes close to the two incidence in Alsace is probably not enough to explain such a dif-
cut-offs of 5 and 10 mm. ference. Data from the European cancer registries show that the
Our study has several limitations. The main one is its small size incidence of CRC in Alsace is one of the highest in Europe [47].
along with its single-center design. Our results should be verified Another probable explanation is the double tendency of our pa-
with a larger scale multicenter trial before the proposed policy thologists to over-read villous histology and high grade dysplasia
could be introduced to current practice. One could consider that [32]. However, the natural history of diminutive adenomas is not
our conclusions are only valid in France; however, this is not the fully known. Is it really necessary to remove them to prevent
case because our results remain similar when using other guide- CRC? At the present time while we await better knowledge on
lines, such as US guidelines. Owing to the differences between their natural history, all neoplastic diminutive polyps should
national surveillance guidelines, it is almost impossible to con- probably be removed during colonoscopy. Overall, the natural
struct a universal algorithm; however, we propose an algorithm history of colorectal adenomas, including diminutive, small, and
on the management of diminutive polyps (● " Fig. 1) that could be advanced adenomas, is still incompletely understood and should
adapted to different guidelines. Moreover, a universal message be the field of future research, especially to assess their real risk
can be drawn from our study: it is possible, as of today and in all of becoming invasive CRC.
countries and facilities without the introduction of any new tech- In summary, 18 – 44 % of diminutive polyps (i. e. 14 – 33 % of all
nology, to discard safely some diminutive polyps without patho- polyps), can be removed and safely discarded without pathologi-
logical examination – at least around 18 % of them without any cal examination with, respectively, 100 % to 98.3 % of patients
risk to the patient. having the same surveillance interval as with pathological exam-
Another limitation is that the discard policy of diminutive polyps ination. A pathological examination would still be required for
is valid only when the number of polyps < 10 mm in size is one or some diminutive polyps: those with an unusual gross appearance
two. When their number is three or more, they all have to be such as ulceration or depression that could reflect malignancy,
examined because a number of three or more adenomas leads those three or more in number, and those isolated one or two in
to a 3-year surveillance interval [8, 29]. Indeed, when proposing number removed from persons without personal history of colo-
a 3-year interval to patients with three or more polyps < 10 mm rectal neoplasm (● " Fig. 1). If such a policy was adopted, the

in size without pathological examination of diminutive ones, we pathological examination could be spared in up to 33 % of all
calculated a 59.4 % rate of over-surveillance owing to the high polyps, lightening the burden for overloaded pathologists and
proportion of nonadenomatous polyps within those polyps. generating significant cost savings.
However, is it really necessary to perform a surveillance colonos-
copy within a 3-year interval for people having three or more
adenomas < 10 mm in size? Some authors have shown that a Acknowledgments
number of three or more nonadvanced adenomas was not an !
independent risk factor for recurrent advanced adenoma within The authors thank all the staff of the Endoscopy Unit and the pa-
4 years [43]. thologists of the Pasteur Hospital of Colmar for their contribu-
Another question remains unanswered: What is the actual risk of tions.
a 5-year surveillance interval for an isolated diminutive adenoma
with advanced pathologic features? Is it really necessary to per- Competing interests: None
form surveillance colonoscopy at 3-year intervals as recommen-
ded by French and US guidelines [8, 29]? Some studies have sug-
gested that a 5-year interval might be sufficient even after
removal of high risk adenomas [44]. Our opinion is that a 5-year

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86 Original article

References 25 Hurlstone DP, Cross SS, Lobo AJ. A 1 mm depressed type IIc minute colo-
1 Atkin WS, Morson BC, Cuzick J. Long-term risk of colorectal cancer after rectal cancer: first reported case and discussion of clinical relevance,
excision of rectosigmoid adenomas. N Engl J Med 1992; 326: 658 – 662 with special reference to endoscopic diagnosis. J Gastroenterol Hepatol
2 Winawer SJ, Zauber AG, Ho MN et al. Prevention of colorectal cancer by 2003; 18: 880 – 884
colonoscopic polypectomy. N Engl J Med 1993; 329: 1977 – 1981 26 Konishi K, Kaneko K, Kurahashi T et al. A comparison of magnifying and
3 Citarda F, Tomaselli G, Capocaccia R et al. Efficacy in standard clinical non magnifying colonoscopy for diagnosis of colorectal polyps: a pro-
practice of colonoscopic polypectomy in reducing colorectal cancer in- spective study. Gastrointest Endosc 2003; 57: 48 – 53
cidence. Gut 2001; 48: 812 – 815 27 Ignjatovic A, East JE, Suzuki N et al. Optical diagnosis of small colorectal
4 Külling D, Christ AD, Karaaslan N et al. Is histological investigation of polyps at routine colonoscopy (Detect InSpect ChAracterise Resect and
polyps always necessary? Endoscopy 2001; 33: 428 – 432 Discard; DISCARD trial): a prospective cohort study. Lancet Oncol
5 Odom SR, Duffy SD, Barone JE et al. The rate of adenocarcinoma in en- 2009; 10: 1171 – 1178
doscopically removed colorectal polyps. Am Surg 2005; 71: 1024 – 28 Van den Broek FJC, Reitsma JB, Curvers WL et al. Systematic review of
1026 narrow-band imaging for the detection and differentiation of neoplas-
6 East JE, Saunders BP. Look, remove, and discard: can narrow-band tic and nonneoplastic lesions in the colon. Gastrointest Endosc 2009;
imaging replace histopathology for small colorectal polyps? It is time 69: 124 – 135
to push the button! Gastrointest Endosc 2007; 66: 953 – 956 29 Winawer SJ, Zauber AG, Fletcher RH et al. Guidelines for colonoscopy
7 Rex DK. Narrow-band imaging without optical magnification for histo- surveillance after polypectomy: a consensus update by the US multi-
logic analysis of colorectal polyps. Gastroenterology 2009; 136: 1174 – society task force on colorectal cancer and the american cancer society.
CA Cancer J Clin 2006; 56: 143 – 159

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8 ANAES: French National Agency for Accreditation and Evaluation in 30 Appelman HD. Should HGD or degree of villous changes in colon polyps
Healthcare. Clinical practice guidelines. Indications for lower gastroin- be reported? CON: high-grade dysplasia and villous features should
testinal endoscopy (excluding population screening) Available at URL: not be part of the routine diagnosis of colorectal adenomas. Am J Gas-
www.has-sante.fr/portail/jcms/c_272 348/indications-for-lower-gas- troentrol 2008; 103: 1329 – 1331
trointestinal-endoscopy-excluding-population-screening. Last acces- 31 Odze RD. Should HGD or degree of villous changes in colon polyps be
sed: 14 October 2010 reported? A balancing view: pathologist-clinician interaction is essen-
9 Hamilton SD, Vogelstein B, Kudo S et al. Tumours of the colon and rec- tial. Am J Gastroentrol 2008; 103: 1331 – 1333
tum: Carcinoma of the colon and rectum. In: Hamilton SR, Aaltonen 32 Denis B, Peters C, Chapelain C et al. Diagnostic accuracy of community
LA (eds). World Health Organization Classification of Tumours. Pathol- pathologists in the interpretation of colorectal polyps. Eur J Gastroen-
ogy and Genetics of Tumours of the Digestive System. Lyon: IARC Press, terol Hepatol 2009; 21: 1153 – 1160
2000: 105 – 119 33 Demers RY, Neale AV, Budev H et al. Pathologist agreement in the inter-
10 Snover DC, Jass JR, Fenoglio-Preiser C et al. Serrated polyps of the large pretation of colorectal polyps. Am J Gastroenterol 1990; 85: 417 – 421
intestine. A morphologic and molecular review of an evolving concept. 34 Jensen P, Krogsgaard MR, Christiansen J et al. Observer variability in the
Am J Clin Pathol 2005; 124: 380 – 391 assessment of type and dysplasia of colorectal adenomas, analyzed
11 Schlemper RJ, Kato Y, Stolte M. Diagnostic criteria for gastrointestinal using Kappa statistics. Dis Colon Rectum 1995; 38: 195 – 198
carcinomas in Japan and Western countries: proposal for a new classi- 35 Rex DK, Alikhan M, Cummings O et al. Accuracy of pathologic interpre-
fication system of gastrointestinal epithelial neoplasia. J Gastroenterol tation of colorectal polyps by general pathologists in community prac-
Hepatol 2000; 15: G49 – 57 tice. Gastrointest Endosc 1999; 50: 468 – 474
12 Dixon MF. Gastrointestinal epithelial neoplasia: Vienna revisited. Gut 36 Yoon H, Martin A, Benamouzig R et al. Inter-observer agreement on his-
2002; 51: 130 – 131 tological diagnosis of colorectal polyps: the APACC study. Gastroenter-
13 Sobin L, Gospodarowicz MK, Wittekind C. UICC, TNM classification of ol Clin Biol 2002; 26: 220 – 224
malignant tumors, 7th edn. New York: Wiley-Blackwell, 2009 37 Terry MB, Neugut AI, Bostick RM et al. Reliability in the classification of
14 Muto T, Bussey HJR, Morson BC. The evolution of cancer of the colon and advanced colorectal adenomas. Cancer Epidemiol Biomarkers Prev
rectum. Cancer 1975; 36: 2251 – 2270 2002; 11: 660 – 663
15 O’Brien MJ, Winawer SJ, Zauber AG et al. The National Polyp Study. Pa- 38 Costantini M, Sciallero S, Giannini A et al. Interobserver agreement in
tient and polyp characteristics associated with high-grade dysplasia in the histologic diagnosis of colorectal polyps: the experience of the
colorectal adenomas. Gastroenterology 1990; 98: 371 – 379 multicenter adenoma colorectal study (SMAC). J Clin Epidemiol 2003;
16 Nusko G, Mansmann U, Partzsch U et al. Invasive carcinoma in colorec- 56: 209 – 214
tal adenomas: multivariate analysis of patient and adenoma character- 39 Saini SD, Kim HM, Schoenfeld P. Incidence of advanced adenomas at sur-
istics. Endoscopy 1997; 29: 626 – 631 veillance colonoscopy in patients with a personal history of colon ade-
17 Matek W, Guggenmoos-Holzmann I, Demling L. Follow-up of patients nomas: a meta-analysis and systematic review. Gastrointest Endosc
with colorectal adenomas. Endoscopy 1985; 17: 175 – 181 2006; 64: 614 – 626
18 Weston AP, Campbell DR. Diminutive colonic polyps: histopathology, 40 Martinez ME, Baron JA, Liebermann DA et al. A pooled analysis of ad-
spatial distribution, concomitant significant lesions, and treatment vanced colorectal neoplasia diagnoses after colonoscopic polypecto-
complications. Am J Gastroenterol 1995; 90: 24 – 28 my. Gastroenterology 2009; 136: 832 – 841
19 Gschwantler M, Kriwanek S, Langner E et al. High-grade dysplasia and 41 Atkin WS, Saunders BP. Surveillance guidelines after removal of colo-
invasive carcinoma in colorectal adenomas: a multivariate analysis of rectal adenomatous polyps. Gut 2002; 51 (Suppl. V): v6 – v9
the impact of adenoma and patient characteristics. Eur J Gastroenterol 42 Schoen RE, Gerber LD, Margulies C. The pathologic measurement of
Hepatol 2002; 14: 183 – 188 polyp size is preferable to the endoscopic estimate. Gastrointest En-
20 Church JM. Clinical significance of small colorectal polyps. Dis Colon dosc 1997; 46: 492 – 496
Rectum 2004; 47: 481 – 485 43 Laiyemo AO, Murphy G, Albert PS et al. Postpolypectomy colonoscopy
21 Butterly LF, Chase MP, Pohl H et al. Prevalence of clinically important surveillance guidelines: predictive accuracy for advanced adenoma at
histology in small adenomas. Clin Gastroenterol Hepatol 2006; 4: 4 years. Ann Intern Med 2008; 148: 419 – 426
343 – 348 44 Brenner H, Chang-Claude J, Seiler CM et al. Case-control study supports
22 Yoo TW, Park DI, Kim YH et al. Clinical significance of small colorectal extension of surveillance interval after colonoscopic polypectomy to at
adenoma less than 10 mm: the KASID study. Hepatogastroenterology least 5 Yr. Am J Gastroenterol 2007; 102: 1739 – 1744
2007; 54: 418 – 421 45 Schoenfeld P. Small and diminutive polyps: implications for colorectal
23 Lieberman D, Moravec M, Holub J et al. Polyp size and advanced histol- cancer screening with computed tomography colonography. Clin Gas-
ogy in patients undergoing colonoscopy screening: implications for CT troenterol Hepatol 2006; 4: 293 – 295
colonography. Gastroenterology 2008; 135: 1100 – 1105 46 Zalis ME, Barish MA, Choi JR et al. CT colonography reporting and data
24 Rex DK, Overhiser AJ, Chen SC et al. Estimation of impact of American system: a consensus proposal. Radiology 2005; 236: 3 – 9
College of Radiology recommendations on CT colonography reporting 47 European Cancer Registries.
for resection of high-risk adenoma findings. Am J Gastroenterol 2009; Available at URL: http://213.169.175.103:5550947. Last accessed: 14
104: 149 – 153 October 2010

Denis B et al. Pathological examination of diminutive polyps … Endoscopy 2011; 43: 81 – 86

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