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ANATOMY
RULES FOR CLASSIFICATIONS DEFINITION OF TNM STAGE GROUPING HISTOPATHOLOGIC TYPE HISTOPATHOLOGIC GRADE (G) PROGNOSTIC FACTORS BIBLIOGRAPHY |
Manual for Staging of Cancer; Fifth Edition; Edited by Irvin D. Fleming, M.D., Jay S. Cooper, M.D., Donald Earl Henson, M.D., Robert V.P. Hutter, M.D., B.J. Kennedy, M.D., Gerald Murphy, M.D., D.S.c., Brian O'Sullivan, M.B., F.R.C.P.C., F.R.C.P.I., Leslie H. Sobin, M.D., John W. Yarbro, M.D., Ph.D.; Copyright 1997, the American Joint Committee on Cancer. Published by Lippincott-Raven Publishers. Chapter 12, pp. 83 - 90.
| C18.0 | Cecum | C19.9 | Rectosigmoid junction |
| C18.1 | Appendix | C20.9 | Rectum |
| C18.2 | Ascending | ||
| C18.3 | Hepatic flexure | ||
| C18.4 | Transverse | ||
| C18.5 | Splenic flexure | ||
| C18.6 | Descending | ||
| C18.7 | Sigmoid | ||
| C18.8 | Overlapping lesion | ||
| C18.9 | Colon, NOS |
The TNM classification for carcinomas of the colon and rectum provides more detail than other staging systems. Compatible with Dukes, the TNM adds greater precision in the identification of prognostic subgroups. The TNM is based on the depth of tumor invasion into the wall of the intestine, extension to adjacent structures, the number of regional lymph nodes involved, and the presence or absence of distant metastasis. The TNM classification applies to both clinical and pathologic staging. Most cancers of the colon or rectum, however, are staged after pathologic examination of the resected specimen. This staging system applies to all carcinomas arising in the colon, rectum, or in the vermiform appendix.
Divisions of the Colon and Rectum:
Cecum
Ascending colon
Hepatic flexure
Transverse colon
Splenic flexure
Descending colon
Sigmoid colon
Rectosigmoid junction
Rectum
Cancers that occur in the anal canal are staged according to the classification used for the anus (see Chapter 13).
Primary Site. The large intestine (colorectum) extends from the terminal ileum to the anal canal. Excluding the rectum and vermiform appendix, the colon is divided into four parts: the right or ascending colon, the middle or transverse colon, the left or descending colon, and the sigmoid colon. The sigmoid is continuous with the rectum which terminates at the anal canal.
The cecum is a large pouch that forms the proximal segment of the right colon. It usually measures 6 cm by 9 cm and is covered with peritoneum. The ascending colon measures 15 to 20 cm in length and is located retroperitoneally. Connecting the ascending colon to the transverse colon is the hepatic flexure which lies under the right lobe of the liver near the duodenum.
The transverse colon lies more anteriorly than the other divisions of the colon. It is supported by the transverse mesocolon which is attached to the pancreas. Anteriorly, its serosa is continuous with the gastrocolic ligament. The transverse colon is connected to the descending colon by the splenic flexure which is located near the spleen and tail of the pancreas. The descending colon, which measures 10 to 15 cm in length, is also located retroperitoneally. The descending colon becomes the sigmoid at the origin of the mesosigmoid. The sigmoid loop extends from the medial border of the left posterior major psoas muscle to the rectum, which begins at the termination of the mesosigmoid.
Approximately 12 cm in length, the rectum extends from the third sacral vertebra to the apex of the prostate gland in the male and to the apex of the perineal body in the female; that is, to a point 4 cm anterior to the tip of the coccyx. It is often defined as the distal 10 cm of the large intestine as measured from the anal verge with a sigmoidoscope. The rectosigmoid segment is usually 10 to 15 cm from the anal mucocutaneous junction. The rectum is covered by peritoneum in front and on both sides in its upper third and only on the anterior wall in its middle third. The peritoneum is reflected laterally from the rectum to form the perirectal fossa and anteriorly the uterine or rectovesical fold. There is no peritoneal covering in the lower third, which is often known as the rectal ampulla. The anal canal, which measures 4 to 5 cm in length, courses downward and backward from the apex of the prostate gland or from the perineal body to the anal verge. (See Fig. 12-1.)
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(Total length of large intestine approximately 150 cm). * The rectosigmoid is of anatomic and surgical importance because of the blood supply and the disappearance of the mesosigmoid. While the rectosigmoid is truly a junction, some authors include 1 inch of the sigmoid above and 1 inch of rectum below and refer to it as the rectosigmoid region. These measurements are APPROXIMATIONS ONLY. Each person is different and these measurements should be used as GUIDELINES ONLY. FIG. 12-1. The anatomic areas of the colon and rectum are: cecum (1); ascending colon (2); hepatic flexure (3); transverse colon (4); splenic fixture (5); descending colon (6); sigmoid (7); rectosigmoid (7.5); rectum (8); anal canal (9);. |
Regional Lymph Nodes. Regional nodes are located: (1) along the course of the major vessels supplying the colon and rectum; (2) along the vascular arcades of the marginal artery; and (3) adjacent to the colon; that is, located along the mesocolic border of the colon. Specifically, the regional lymph nodes are the pericolic and perirectal nodes and those found along the ileocolic, right colic, middle colic, left colic, inferior mesenteric artery, superior rectal (hemorrhoidal), and internal iliac arteries.
For pN, the number of lymph nodes sampled should be recorded. It is desirable to obtain at least 12 lymph nodes in radical colon resections; however, in cases in which tumor is resected for palliation or in patients who have received pre-operative radiation, only a few lymph nodes may be present.
The regional lymph nodes for each segment of the colon are:
| SEGMENT | REGIONAL LYMPH NODES |
| Cecum and appendix | Anterior cecal, posterior cecal, ileocolic, right colic |
| Ascending colon | Ileocolic, right colic, middle colic |
| Hepatic flexure | Middle colic, right colic |
| Transverse colon | Middle colic |
| Splenic flexure | Middle colic, left colic, inferior mesenteric |
| Descending colon | Left colic, inferior mesenteric, sigmoid |
| Sigmoid colon | Inferior mesenteric, superior rectal, (hemorrhoidal), sigmoidal, sigmoid mesenteric |
| Rectosigmoid | Perirectal, left colic, sigmoid mesenteric, sigmoidal, inferior mesenteric, superior rectal (hemorrhoidal), middle rectal (hemorrhoidal) |
| Rectum | Perirectal, sigmoid mesenteric, inferior mesenteric, lateral sacral presacral, internal iliac, sacral promontory (Gerota's), superior rectal (hemorrhoidal), middle rectal (hemorrhoidal), inferior rectal (hemorrhoidal) |
Metastatic Sites. Although carcinomas of the colon and rectum can metastasize to almost any organ, the liver and lungs are the most common sites. Seeding of other segments of the colon or small intestine can also occur.
Clinical Staging. Clinical assessment is based on medical history, physical examination, routine and special imaging procedures, sigmoidoscopy, colonoscopy with biopsy, and special examinations designed to demonstrate the presence of extracolonic metastasis, for example, chest films, liver function tests, and liver scans.
Pathologic Staging. Colorectal cancers are usually staged after pathologic examination of the resected specimen and surgical exploration of the abdomen. The definition of in situ carcinoma pTis includes cancer cells confined within the glandular basement membrane (intraepithelial) or lamina propria (intramucosal) with no extension through the muscularis mucosae into the submucosa. This definition of pTis is different from that used for the other divisions of the gastrointestinal tract. Neither intraepithelial nor intramucosal carcinomas of the large intestine have a significant potential for metastasis.
Tumor that invades the stalk of a polyp is classified according to the pT definitions adopted for colorectal carcinomas. For instance, tumor that is limited to the lamina propria is listed as pTis, whereas tumor that has invaded the muscularis mucosae and entered the submucosa of the stalk is classified T1.
Lymph nodes are classified N1 or N2 according to the number involved with metastatic tumor. Involvement of 1 to 3 nodes is N1.
Patients with tumor located on the serosal surface as a result of direct extension through the colon are assigned T4. Seeding of abdominal organs, for instance, the distal ileum from a carcinoma of the transverse colon, is considered discontinuous metastasis and should be recorded as M1. Metastatic nodules or foci found in the pericolic or perirectal fat or in adjacent mesentery (mesocolic fat) without evidence of residual lymph node tissue are equivalent to regional lymph node metastasis. Multiple metastatic foci seen microscopically only in the pericolic fat should be considered as metastasis in a single lymph node for classification. A tumor nodule greater than 3 mm in diameter in the perirectal or pericolic fat without histologic evidence of a residual node in the nodule is classified as regional perirectal or pericolic lymph node metastasis. However, a tumor nodule 3 mm or less in diameter is classified in the T category as a discontinuous extension, that is T3.
Metastasis in the external iliac or common iliac lymph nodes is classified M1.
If the tumor recurs at the site of surgery, it is anatomically assigned to the proximal segment of the anastomosis.
| TX | Primary tumor cannot be assessed |
| T0 | No evidence of primary tumor |
| Tis | Carcinoma in situ: intraepithelial or invasion of lamina propria* |
| T1 | Tumor invades submucosa |
| T2 | Tumor invades muscularis propria |
| T3 | Tumor invades through the muscularis propria into the subserosa, or into nonperitonealized pericolic or perirectal tissues |
| T4 | Tumor directly invades other organs or structures, and/or perforates visceral peritoneum** |
*Note: Tis includes cancer cells confined within the glandular basement membrane (intraepithelial) or lamina propria (intramucosal) with no extension through the muscularis mucosae into the submucosa.
**Note: Direct invasion in T4 includes invasion of other segments of the colorectum by way of the serosa; for example, invasion of the sigmoid colon by a carcinoma of the cecum.
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*Dukes B is a composite of better (T3 N0 M0) and worse (T4 N0 M0) prognostic groups, as is Dukes C (Any T N1 M0 and Any T N2 M0)
Adenocarcinoma in situ*
Adenocarcinoma
Mucinous carcinoma, (colloid type) (greater than 50% mucinous
carcinoma)
Signet ring cell carcinoma (greater than 50% signet ring cell)
Squamous cell (epidermoid) carcinoma Adenosquamous carcinoma
Small cell carcinoma
Undifferentiated carcinoma
Carcinoma, NOS
*The terms "high grade dysplasia" or "severe dysplasia" may be used as synonyms for in situ adenocarcinoma or in situ carcinoma. These cases should be assigned pTis.
Bauer K, Bagwell C, Giaretti W, et al: Consensus review of the clinical utility of DNA flow cytometry in colorectal cancer. Cytometry 14:486-491, 1993
Butch RJ, Stark DD, Wittenberg J, et al: Staging rectal cancer by MR and CT. AJR Am J Roentgenol 146:1155-1160, 1986
Chapuis PH, Fisher R, Dent DF, et al: The relationship between different staging methods and survival in colorectal carcinoma. Dis Colon Rectum 28:158-161, 1985
Dukes CE: Cancer of the rectum: an analysis of 1000 cases. J Pathol Bacteriol 50:527-539, 1940
Fenoglio-Preiser CM, Hutter RVP: Colorectal polyps: pathologic diagnosis and clinical significance. Cancer J Clin 35:322-344, 1985
Fielding LP: Clinicopathological staging for colorectal cancer: an International Documentation System (IDS) and an International Comprehensive Anatomical Terminology (ICAT). J Gastroenterol Hepatol, 1991
Fielding LP, Ballantyne GH: Classification systems for staging colorectal cancer. Problems Gen Surg 4:39-53, 1987
Fielding LP, Pettigrew N: College of American Pathologists Conference XXVI on clinical relevance of prognostic markers in solid tumors: report of the Colorectal Working Group. Arch Pathol Lab Med 119:1115-1121, 1995
Fielding LP, Phillips RK, Frey JS, et al: The prediction of outcome after curative resection for large bowel cancer. Lancet 2:904-907, 1986
Fielding LP, Phillips RK, Hittinger R: Factors influencing mortality after curative resection for large bowel cancer in elderly patients. Lancet 1:595-597, 1989
Griffin MR, Bergstralh EJ, Coffey RJ, et al: Predictors of survival after curative resection of carcinoma of the colon and rectum. Cancer 60:2318-2324, 1987
Harrison JC, Dean PJ, El-Zeky F, et al: From Dukes through Jass: pathological prognostic indicators in rectal cancer. Hum Pathol 25:498-505, 1994
Henson DE, Hutter RVP, Sobin LH, et al: Protocol of the examination of specimens removed from patients with colorectal carcinoma. Arch Pathol Lab Med 118:122-125, 1994
Hermanek P: Colorectal carcinoma. Histopathological diagnosis and staging. Baillieres Clin Gastroenterol 3:511-529, 1989
Hermanek P: Problems of pTNM classification of carcinoma of the stomach, colorectum and anal margin. Pathol Res Pract 181:296-300, 1986
Hermanek P, Gall FP: Early (microinvasive) colorectal carcinoma: pathology, diagnosis, surgical treatment. Int J Colorectal Dis 1:79-84, 1986
Hermanek P, Giedl J, Dworak O: Two programs for examination of regional lymph nodes in colorectal carcinoma with regard to the new pN classification. Pathol Res Pract 185:867-873, 1989
Hermanek P, Guggenmoos-Holzmann I, Gall FP: Prognostic factors in rectal carcinoma. A contribution to the further development of tumor classification. Dis Colon Rectum 32:593-599, 1989
Hermanek P, Henson DE, Hutter RVP, Sobin LH: TNM Supplement 1993: a commentary on uniform use. Berlin: Springer-Verlag, 1993
Hermanek P, Sobin LH: Colorectal carcinoma. In Hermanek P, Gospodarowicz MK, Henson DE, et al (Eds.), Prognostic factors in cancer. Berlin: Springer-Verlag, 1995
Herrera-Ornelas L, Justiniano J, Castillo, N, et al: Metastases in small lymph nodes from colon cancer. Arch Surg 122:1253-1256, 1987
Jass JR, Atkin WS, Cuzick J, et al: The grading of rectal cancer: historical perspectives and a multivariate analysis of 447 cases. Histopathology 10:437-459, 1986
Jass JR, Love SB, Northover JMA: A new prognostic classification of rectal cancer. Lancet i:1303-1306, 1987
Jass JR, Mukawa K, Goh HS, et al: Clinical importance of DNA content in rectal cancer measured by flow cytometry. J Clin Pathol 42:254-259, 1989
Jass JR, Sobin LH: Histological typing of intestinal tumours. WHO International Histological Classification of Tumours, 2nd ed. Berlin-New York: Springer-Verlag, 1989
Kokal W, Sheibani K, Terz J, et al: Tumor DNA content in the prognosis of colorectal carcinoma. JAMA 255:3123-3127, 1986
Kotanagi H, Fukuoka T, Shibata Y, et al: Blood vessel invasions in metastatic nodes for development of liver metastasis in colorectal cancer. Hepato-Gastroenterol 42:771-774, 1995
Lindmark G, Gerdin B, Sundberg C, et al: Prognostic significance of the microvascular count in colorectal cancer. J Clin Oncol 14:461-466, 1996
Lipper S, Kahn LB, Ackerman LV: The significance of microscopic invasive cancer in endoscopically removed polyps of the large bowel: a clinicopathologic study of 51 cases. Cancer 52:1691, 1983
Minsky BD, Mies C, Rich TA, et al: Lymphatic vessel invasion is an independent prognostic factor for survival in colorectal cancer. Int J Radiat Oncol 17:311-318, 1989
Newland RC, Chapuis PH, Pheils MT, et al: The relationship of survival to staging and grading of colorectal carcinoma: a prospective study of 503 cases. Cancer 47:1424-1429, 1981
Ondero H, Maetani S, Nishikawa T, et al: The reappraisal of prognostic classifications for colorectal cancer. Dis Colon Rectum 32:609-614, 1989
Phillips RKS, Hittinger R, Blesovsky L, et al: Large bowel cancer: surgical pathology and its relationship to survival. Br J Surg 71:604-610, 1984
Qizilbash AH: Pathologic studies in colorectal cancer: a guide to the surgical pathology examination of colorectal specimens and review of features of prognostic significance. Pathol Annu 17(1): 146, 1982
Scott KWM, Grace RH: Detection of lymph node metastases in colorectal carcinoma before and after fat clearance. Br J Surg 76:1165-1167, 1989
Scott NA, Rainwater LM, Wieland HS, et al: The relative prognostic value of flow cytometric DNA analysis and conventional clinicopathologic criteria in patients with operative rectal carcinoma. Dis Colon Rectum 30:513-520, 1987
Shepherd NA, Saraga EP, Love SB, et al: Prognostic factors in colonic cancer. Histopathology 14:613-620, 1989
Steinberg SM, Barkin JS, Kaplan RS, et al: Prognostic indicators of colon tumors: the gastrointestinal tumor study group experience. Cancer 57: 1866-1870, 1986
Talbot IC, Ritchie S, Leighton MH, et al: The clinical significance of invasion of veins by rectal cancer. Br J Surg 67:439-442, 1980
Talbot IC, Ritchie S, Leighton MH, et al: Spread of rectal cancer within veins: histologic features and clinical significance. Am J Surg 141:15-17, 1981
Williams NS, Durdey P, Qwihe P, et al: Pre-operative staging of rectal neoplasm and its impact on clinical management. Br J Surg 72:868-874, 1985
Wolmark N, Fisher B, Wieand HS: The prognostic value of the modifications of the Dukes' C class of colorectal cancer: an analysis of the NSABP clinical trials. Ann Surg 203:115-122, 1986
Wolmark N, Fisher ER, Wieand HS, et al: The relationship of depth of penetration and tumor size to the number of positive nodes in Dukes' C colorectal cancer. Cancer 53:2707-2712, 1984