








 |
CGMH
Administration
Center |
No.199, Tunghwa Rd.,
Taipei, Taiwan, R.O.C |

886-2-27135211 |
|
|
|
Correlation of the Morphology and Size of
Colonic Polyps with Their Histology |
|
Tze-Vun Fong, MD
Seng-Kee Chuah, MD
Shue-Shian Chiou, MD
King-Wah Chiu, MD
Chia-Chang Hsu, MD
Yu-Chun Chiu, MD
Keng-Liang Wu, MD
Yeh-Ping Chou, MD
Guan-Yeow Ong, MD
Chi-Sin Changchien, MD
|
 |
 |
|
Background:
Colonic adenomatous polyps are premalignant lesions; early
recognition and use of a polypectomy for these polyps can
reduce the occurrence of colorectal cancer. The purposes of
this study were to evaluate the complications of polypectomy
and the relationship between the morphology and size of colonic
polyps and their histology.
Methods:
Data on colonic polyps from 324 patients who received a polypectomy
between April 1998 and December 2001 were collected. These
included 207 men and 117 women, ranging in age between 17
and 86 years old, and who had had a colonoscopy or sigmoidoscopic
examination. A polypectomy was performed on those colonic
polyps discovered, and their morphology, size, and histology
were analyzed.
Results:
The histological findings of these polyps included adenoma,
carcinoma, hyperplastic, and inflammatory polyps. One and
a half percent (n = 6) were carcinomas, all of which belonged
to the Yamada III or IV polyp group and were more than 1 cm
in size, except for 1 polyp which was 0.7 cm. One case was
complicated by colon perforation, and 2 cases experienced
mild bleeding with no need for a blood transfusion or hospitalization.
Conclusions:
Morphology and size are closely related to the malignant change
in colonic polyps. Colonic polyps with a size greater than
1 cm and classified as Yamada type III or IV have a higher
potential for malignant change, and a polypectomy should be
considered when they are discovered. A polypectomy is a safe
procedure with only minor complications.
(Chang Gung Med J 2003;26:339-43)
Key words:
colon polyp, polypectomy.
|
| |
 |
| The incidence of colorectal cancer has increased in recent
years. Most studies support adenomatous colonic polyps being
considered precursors to the development of colorectal cancer.(1)
The size of the polyps was shown to be closely related to malignant
change, but invasive cancer was found even in polyps that were
less than 1 cm.(2) Although up to 2/3 of colorectal carcinomas
might have developed from adenomatous polyps, the flat or depressed
lesion also plays an important role.(3,4) Therefore, early recognition
of these lesions and a colonoscopic or sigmoidoscopic polypectomy
are mandatory, but its safety is also a matter of concern. Some
studies have reported that the rate of complications for polypectomies
ranged from 0.3% to 6.1%, which included hemorrhage or colon
perforation.(5-8) The purposes of this retrospective study were
to evaluate the relationship between morphology and size of
colonic polyps and their histology, and the safety of performing
polypectomies by colonoscopy or sigmoidoscopy.
METHODS
Three hundred and twenty-four patients who had received a
polypectomy for colonic polyps between April 1998 and December
2001 were retrospectively analyzed. The ages ranged from 17
to 86 years old. In total, 400 colonic polyps were resected
either by snare polypectomy or biopsy forceps for smaller
polyps. After the patients were well prepared with polyethylene
glycol or magnesium citrate, the endoscope was introduced
up to the cecum when performing a colonoscopy or 60 cm from
the anal verge if a sigmoidoscopic examination was arranged.
Once the polyps were found, they were removed by any 1 of
the methods mentioned above. The retrieved polyps were sent
to a pathologist for size measurement and histological review.
Macroscopic appearances of the polyps were categorized according
to the Yamada classification.(9)
RESULTS
Altogether, we identified a total of 400 polyps in 324 patients.
The indications for colonoscopy or a sigmoidoscopic examination
included hematochezia (22.5%), diarrhea (21.3%), abdominal
pain (20.0%), constipation (13.8%), and other less common
indications such as tenesmus, a colonic polyp history, small-caliber
stool, or positive fecal occult blood (Table 1). Two hundred
seventy-nine patients had a single lesion, while 28 patients
had 2 lesions, and 17 patients had 3 or more lesions. The
histological findings of these polyps included adenomas (73.7%),
hyperplastic polyps (11.0%), carcinomas (1.5%), and others
(13.8%) such as inflammation, granulation tissue, retention
polyps, lipomas, juvenile polyps, and so forth (Table 2).
Morphologically, the polyps could be categorized into Yamada
types I to IV, that is 10.2% (41/400) were type I, 20.2% (81/400)
were type II, 33.7% (135/400) were type III, and 35.7% (143/400)
were type IV. Six cases of carcinoma were identified, of which
5 were Yamada type IV polyps with a size greater than 1 cm,
and the other was a 0.7-cm polyp belonging to the Yamada type
III group. Four of these malignant polyps had irregular surfaces,
while 2 showed a smooth reddish head when viewed macroscopically
by colonoscopy or sigmoidoscopy (Table 3).
One patient was complicated by colon perforation after a polypectomy
for a 1.2-cm Yamada type III polyp which was later identified
as being a tubular adenoma by a pathologist. Two other cases
had mild bleeding after the polypectomy, but neither blood
transfusion nor hospitalization was needed (Table 4).
DISCUSSION
Most studies support adenomatous polyps being neoplastic
precursors of colorectal cancers.(1,10) An analysis of 7000
polyps by Shinya revealed that 2.8%, 8.4%, and 9.5% of tubular
adenomas, tubulovillous adenomas, and villous adenomas contained
malignant cells, respectively, which implied that colon cancerous
change was directly proportional to the presence of a villous
component.(2,11)
In our series, all 6 cases of cancer belonged to Yamada III
or IV type , and there were no malignancies for Yamada I or
II polyps. More than 95% (120/122) of polyps of Yamada types
I and II were less than 1 cm in size. Apparently, size plays
a very important role in predicting malignancy. Atkin et al.
stated that a polyp size of 1 cm or greater had a significantly
increased risk (relative risk of 3.3) of developing subsequent
colorectal cancer; but those with polyps less than 1 cm did
not have an increased risk of cancer.(12) Larger polyps tend
to have a greater villous component and are more likely to
harbor foci of carcinoma.
Carcinomas are histologically detected in 0.1% of polyps measuring
less than 0.5 cm in diameter; this increases to 1.0% with
1-cm-diameter polyps and reaches 40% with polyps exceeding
2 cm.(13,14) In our study, no cancer was found in polyps of
less than 0.5 cm. Only 1 polyp, 0.8% (1/120), between 0.6
and 1.0 cm contained a malignancy. The rate of malignancy
increased to 7.1% (5/70) for polyps greater than 1 cm. This
may imply that the risk of malignant change in polyps of less
than 1 cm is very low; a polypectomy for those polyps may
not be necessary, and thus the cost and complication rate
of polypectomies can also be reduced. Hofstad claimed that
leaving polyps up to 1 cm in diameter may be considered safe,
in terms of avoiding development of invasive carcinomas, provided
that annual endoscopic follow-up examinations are carried
out.(15,16) Allan et al. removed a total of 1964 diminutive
polyps(?0.5 cm in diameter), of which 40.7% were adenomatous
and only 0.26% contained atypical cells. This further supports
the chances of diminutive polyps being cancerous or containing
atypical cells being very low, and that removal is not necessary
for these smaller polyps.(17,18)
However, in our daily practice, we eradicate all polyps even
if they are less than 1 cm to prevent adenomatous polyps from
progressing to malignant transformation. Rembacken et al.
reported that 63% of their lesions were polypoid, the remaining
37% were flat and depressed lesions. The overall risk of a
polypoid lesion containing early cancer was 8% (17/204) compared
with 14% (17/119) for flat lesions.(3) No flat lesion was
discovered in our study. The possible reasons were poor preparation
of the colon, and less frequent use of dye sprays. Forty-four
lesions were hyperplastic polyps and were smaller lesions;
some reports still reveal that dysplasia also coexists with
hyperplastic polyps.(19,20)
The reported overall complication rate after a polypectomy
ranges from 0.2% to 6.1%. The most common complication is
bleeding, followed by transmural burn, perforation, and snare
entrapment.(5-8,21,22) The incidence of complications in colonoscopic
polypectomies in this series was 0.7% (3/400). Two cases were
complicated by mild bleeding which improved after conservative
treatment without necessity for a blood transfusion.
One perforation occurred after a polypectomy was performed
for a 1.2-cm polyp which belonged to Yamada type III and was
located on the descending colon. Lack of experience may have
been the main cause for this. Therefore, we suggest that supervision
by a senior endoscopist is mandatory when performing an endoscopic
polypectomy. In conclusion, polyps greater than 1 cm and belonging
to Yamada type III or IV have a higher potential for malignant
change, and resection should be considered. A polypectomy
is a safe procedure despite minor complications.
|
 |
 |
|
REFERENCES
1. Lambert R. Early diagnosis and prevention of sporadic
colorectal cancer. Endoscopy 2001;33:1042-64.
2. Shinya H, Wolff WI. Morphology, anatomic distribution
and cancer potential of colonic polyps. Ann Surg 1979; 190:679-83.
3. BJ Rembacken. Flat and depressed colonic neoplasms:
a prospective study of 1000 colonoscopies in the UK. Lancet
2000;355:1211-4.
4. Kuramoto S, Oohara T. Flat early cancers of the
large intestine. Cancer 1989;64:451-7.
5. Nivatvongs S. Complications in colonoscopic polypectomy:
An experience with 1555 polypectomies. Dis Colon Rectum 1986;29:825-30.
6. Smith LE. Fiberoptic colonoscopy: complications
of colonoscopy and polypectomy. Dis Colon Rectum 1976;19:407-12.
7. Webb WA. Experience with 1000 colonoscopic polypectomies.
Ann Surg 1985;201:626-32.
8. Gibbs DH, Opelka FG, Beck DE, Hicks TC, Timmcke
AE, Gathright JB Jr. Postpolypectomy colonic hemorrhage. Dis
Colon Rectum 1996;39:806-10.
9. T. Yamada, H. Fukutomi. Protruding lesions of the
stomach. I To CHYOU(Japanese) 1966;Vol 1;P145-50.
10. Bond JH. Clinical evidence for the adenoma-carcinoma
sequence, and the management of patients with colorectal adenomas.
Semin Gastrointest Dis 2000;11:176-84.
11. Grinnell RJ. Benign and malignant adenomas polyps
and papillary adenomas of the colon and rectum : an analysis
of 1856 tumors in 1335 patients. Int Abstr Surg 1958; 106:519.
12. Atkin WS, Morson BC, Cuzick J. Long-term risk of
colorectal cancer after excision of rectosigmoid adenomas.
N Engl J Med 1992;326:658-62.
13. Tung SY, Wu CS. Endoscopic treatment of colorectal
polyps and early cancer. Dig Dis Sci 2001;46:1152-6.
14. Day DW, Morson BC. The pathogenicity of colorectal
cancer. Philadelphia, WB Saunders, 1978, pp 58-71.
15. B Hofstad. Growth of colorectal polyps: resection
and evaluation of unresected polyps for a period of three
years. Gut 1996;39:449-56.
16. Hoff G. Epidemiology of polyps in the rectum and
colon Recovery and evaluation of unresected polyps 2 years
after detection. Scand J Gastroenterol 1986;21:853-62.
17. Allan P. Diminutive colonic polyps: histopathology,
spatial, distribution, concomitant significant lesions, and
treatment complications. AJG-1995;90:24-8
18. Tedesco FJ. Diminutive polyps: histopathology,
spatial distribution and clinical significance. Gastrointest
Endosc 1982;28:1-5.
19. Teoh HH, Delahunt B, Isbister WH. Dysplastic and
malignant areas in hyperplastic polyps of the large intestine.
Pathology 1989;21:138-42.
20. McCann BG. A case of metaplastic polyposis of the
colon associated focal adenomatous change and metachronous
adenocarcinomas. Histopathology 1998;13: 703-5.
21. Rosen L, Bub DS, Reed JF 3rd, Mastase SA. Hemorrhage
following colonoscopic polypectomy. Dis Colon Rectum 1993;36:1126-31.
22. Petroski D. Postpolypectomy hemorrhage managed
by chemical cautery. Gastrointest Endosc 1982;28:94-5.
|
 |
 |
|
From the Section of Gastroenterology, Division of Hepatogastroenterology,
Department of Internal Medicine, Chang Gung Memorial Hospital,
Kaohsiung.
Received: Nov. 18, 2002;
Accepted: Feb. 17, 2005
Address for reprints: Dr. Shue-Shian Chiou, Division of Hepatogastroenterology,
Department of Internal Medicine, Chang Gung Memorial Hospital.
123, Dabi Road, Niaosung Shiang, Kaohsiung, Taiwan 833, R.O.C.
Tel.: 886-7-7317123 ext. 8301;
Fax: 886-7-7322402;
E-mail: kyutarou@hotmail.com
|
|