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Malignant Colon Polyps

AndreaM.Petrucci andMarianaBerho
62
Refer toAlgorithm inFig. 62.1
A. Non-invasive Polyps
Carcinoma in situ, high-grade dysplasia or intramucosal adenocarcinoma are all terms used to describe an adenomatous polyp displaying a high degree of cellular and architectural atypia that is conned to the lamina propria. The mucosal lining of the colon is divided into 3 components: the epi­thelium, the lamina propria and the muscula­ris mucosa. While in adenomas with high grade dysplasia/carcinoma in situ the lamina propria is not involved by tumor, intramuco­sal adenocarcinoma is characterized by spill­age of the neoplastic cells beyond the basement membranes of the colonic crypts into the lamina propria. Due to absence of lymphatics in the lamina propria of the colon and rectum, none of these lesions have meta­static potential. The TNM classication groups these lesions into the Tis category and although they have the potential for invasion into the wall of the colon/rectum, polypec­tomy is sufcient if completely resected.
A. M. Petrucci Department ofColorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA
M. Berho (*) Department ofPathology, Cleveland Clinic Florida, Weston, FL, USA e-mail: berhom@ccf.org
B. Malignant Polyps
A “malignant” polyp is dened as the pres­ence of adenocarcinoma that extends beyond the basement membrane. It is important to assess specic characteristics of the polyp in order to decide whether further, more aggres­sive treatment is needed for adequate removal. Invasive polyps can be pedunculated (C) or sessile (D). Pedunculated polyps contain a head, neck and stalk whereas sessile polyps are at. In addition to the morphology of the polyp, important histopathological features including grade of differentiation, the pres­ence of lymphovascular invasion, perineural invasion or tumor budding as well as inade­quate resection margins (<2 mm) all play a very important role in predicting more aggres­sive disease in invasive polyps which will be discussed later.
C. Pedunculated Polyps
Adenocarcinoma in a pedunculated polyp is differently managed according to the loca­tion of the invasive cancer in the polyp. The Haggitt’s classication was rst described by Haggitt et al. in 1985 and is used to assess adenocarcinoma that invades into the submu­cosa in pedunculated polyps. It is a 4-level classication system where levels 1 through 4 indicate adenocarcinoma limited to the head, neck, stalk and base of the polyp respectively (Fig.62.2). Pedunculated polyps of Haggitt’s level 1–3 have a <1% risk of lymph node metastasis therefore can be managed by
© Springer Nature Switzerland AG 2020 S. R. Steele etal. (eds.), Clinical Decision Making in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-65942-8_62
479
480
Adenocarcinoma
Sessile adenoma
Le
Le
Le
Le
Pedunculated adenoma
Le
Fig. 62.1 Algorithm for malignant colonic polyps
A. M. Petrucci and M. Berho
vel 0
Propria
Adenomatous
epithelium
Normal colonic
mucosa
Muscularis
mucosae
Adenocarcinoma
Submucosa
Muscularis
Propria
Subserosal connective tissue
vel 1
vel 2
vel 3
vel 4
Submucosa
Muscularis
Subserosal connective tissue
Fig. 62.2 Demonstration of the different levels of invasion between a pedunculated (right) and a sessile (left) adenoma. (With permission Nivatvongs 2002 © Elsevier)
SM1 SM2 SM3
62 Malignant Colon Polyps
481
simple polypectomy, given that they have favorable histological features. Haggitt’s level 4 is equivalent to a sessile polyp and they are managed similarly. Any suspicious polyp should be tattooed at the site in order to locate it as needed.
D. Sessile Polyps
Adenocarcinoma in a sessile polyp is usu­ally managed with surgical resection, to include a formal lymphadenectomy given the correlation between the level of invasion with the risk of further lymph node involve­ment. The level of invasion is characterized by the Kikuchi classication, which divides the submucosa into three depths of involve­ment: sm1 describes penetration of the upper third of the submucosa, sm2 involves the middle third and sm3 describes deep inva­sion to the lower third level, abutting the inner surface of the muscularis propria (Fig. 62.3). Tumor extending to the lower third were found to have up to a 23% risk of lymph node metastasis, hence the need for a formal bowel resection regardless if they were completely excised or removed piece­meal. It may not always be possible for the pathologist to assess the different levels of submucosal invasion depending on the qual­ity of the specimen that is provided. A recent systematic review showed that submucosal invasion >1 mm corresponded with higher rates of lymph node metastasis, hence the need for formal surgical resection. Moreover, it has recently been suggested that the area of tumor involvement in which both width and
depth of invasion are considered may be a better way to stratify risk of lymph node metastasis.
E. Features
As mentioned earlier, there are many fac­tors that play a signicant role in the manage­ment of malignant polyps. Size, morphology, margin status, degree of differentiation and histopathological features including lympho­vascular and perineural invasion and tumor budding are all carefully assessed since they are all predictors of more aggressive tumors. Polyps <5mm in size are usually benign; those ranging from 1.5 to 3.5cm carry up to a 43% risk of malignancy and should be approached with caution. Margin status is a concern since it correlates with recurrence; polyps with involved margins or margins <1mm from the cut edge correlates with recurrences ranging from 21 to 33% therefore the acceptable mar­gin should be > or = to 2mm. Traditionally, the grades of differentiation were described as grade 1 (well- differentiated), grade 2 (moder­ately-differentiated), grade 3 (poorly differen­tiated, including intestinal-type, signet ring cell or mucinous adenocarcinoma) and grade 4 (undifferentiated, including medullary carci­nomas with high microsatellite instability). More recently the College of American Pathologists has recommended to categorize grade of differentiation in colorectal tumors into low grade (well and moderately differenti­ated adenocarcinoma) and high grade (poorly differentiated and undifferentiated adenocarci­noma). The degree of differentiation correlates
Submucosa
Fig. 62.3 Levels of submucosal invasion in a malignant sessile polyp. With author’s permission. (With permission Nivatvongs 2002 © Elsevier)
482
A. M. Petrucci and M. Berho
with lymph node involvement. Blumberg etal. looked at pathological factors and the risk of lymph metastasis in rectal cancer and found that well-and -moderately differentiated tumors had a 14% risk of lymph node metasta­sis whereas the risk increased to 30% for poorly differentiated lesions. Lymphovascular invasion is an important prognostic factor. The lymphatic channels are usually found in the supercial submucosa and within the muscula­ris mucosa, which is why early lesions within the mucosa have a very low risk of lymph node involvement. Blumberg etal. also found that when lymphovascular invasion is present in a malignant polyp, there is a 33% chance of lymph node metastasis whereas those without lymphovascular invasion only had a 14% risk of positive nodes making this marker a poor prognostic factor. Although tumor budding, which refers to a small clusters of undifferenti­ated cancer cells, has been found to be a poor prognosticator, its utility in clinical practice is limited due to the lack of standardization in the pathological assessment.
In addition, microstaging of malignant polyps to include the depth and width of malignant invasion helps predict lymph node metastasis. Ueno etal. showed that a depth of 2000 um and a width of 4000 um corre­lated with a 18.2% and a 17.1% risk of lymph node metastasis respectively, compared to a <5% risk in polyps with invasion below these values, making these useful histopathologic features to consider.
F. Surveillance
According to the 2016 National Comprehensive Cancer Network (NCCN) guidelines, surveillance after a polypectomy for Tis/T1N0M0 malignant lesion consists of a colonoscopy at 1year following removal. If at the time of colonoscopy, there is no sign of recurrence or advanced adenoma, the interval can be extended to 3years followed by every 5years after that (NCCN).
G. Resection
Colectomy can be performed either open or laparoscopically, depending on the level of experience of the surgeon, and should include a formal lymphadenectomy, includ-
ing the identication of lymph nodes at the origin of the feeding vessel. Any suspicious node seen during surgery outside of the resection margins should be removed and sent to pathology as well. The requirements for N staging consist of the identication of a minimum of 12 lymph nodes in order to be considered a complete and adequate resec­tion (NCCN).

Suggested Reading

Aarons CB, Shanmugan S, Bleier JI. Management of
malignant colon polyps: current status and controver­sies. World J Gastroenterol. 2014;20(43):16178–83.
Beaton C, Twine CP, Williams GL, Radcliffe
AG. Systematic review and meta-analysis of histo­pathological factors inuencing the risk of lymph node metastasis in early colorectal cancer. Color Dis. 2013;15(7):788–97.
Blumberg D, Paty PB, Guillem JG, Picon AI, Minsky BD,
Wong WD, et al. All patients with small intramural rectal cancers are at risk for lymph node metastasis. Dis Colon Rectum. 1999;42(7):881–5.
Bujanda L, Cosme A, Gil I, Arenas-Mirave JI.Malignant
colorectal polyps. World J Gastroenterol. 2010;16(25):3103–11.
Fleming M, Ravula S, Tatishchev SF, Wang HL.Colorectal
carcinoma: pathologic aspects. J Gastrointest Oncol. 2012;3(3):153–73.
Haggitt RC, Glotzbach RE, Soffer EE, Wruble
LD.Prognostic factors in colorectal carcinomas aris­ing in adenomas: implications for lesions removed by endoscopic polypectomy. Gastroenterology. 1985;89(2):328–36.
Kikuchi R, Takano M, Takagi K, Fujimoto N, Nozaki
R, Fujiyoshi T, et al. Management of early invasive colorectal cancer. Risk of recurrence and clinical guidelines. Dis Colon Rectum. 1995;38(12):1286–95.
Nascimbeni R, Burgart LJ, Nivatvongs S, Larson DR.Risk
of lymph node metastasis in T1 carcinoma of the colon and rectum. Dis Colon Rectum. 2002;45(2):200–6.
Nivatvongs S.Surgical management of malignant colorec-
tal polyps. Surg Clin North Am. 2002;82(5):959–66.
Ramirez M, Schierling S, Papaconstantinou HT, Thomas
JS.Management of the malignant polyp. Clin Colon Rectal Surg. 2008;21(4):286–90.
Suzuki T, Sadahiro S, Mukoyama S, Ishikawa K, Yasuda
S, Tajima T, et al. Risk of lymph node and distant metastases in patients with early invasive colorectal cancer classied as Haggitt’s level 4 invasion: image analysis of submucosal layer invasion. Dis Colon Rectum. 2003;46(2):203–8.
Ueno H, Mochizuki H, Hashiguchi Y, Shimazaki H, Aida
S, Hase K, etal. Risk factors for an adverse outcome in early invasive colorectal carcinoma. Gastroenterology. 2004;127(2):385–94.

Colonic Conditions: Adenomatous Polyps

StevenA.Lee-Kong andP.RaviKiran
63
Refer toAlgorithm inFig. 63.1
A. The association between colorectal adenoma-
tous polyps and colorectal cancers (CRC) was rst described by Lockhart-Mummery and Dukes in 1927. This association set the stage for the later recognition that adenoma­tous tissue is a precursor to the development of CRC. The “adenoma to carcinoma” sequence was further elucidated by the iden­tication of somatic mutations associated with this progression by Vogelstein etal. in
1988. These authors analyzed both colorectal adenomas of varying size and carcinomas for somatic mutations in known colorectal cancer- associated genes. Mutations in ras genes were more commonly identied in large adenomas and cancers as compared to smaller adenomas. In advanced adenomas and carcinomas, as compared to smaller ade­nomas, chromosomal sequences were also lost in chromosomal regions associated with
S. A. Lee-Kong Department ofSurgery, Columbia University, New York, NY, USA
P. R. Kiran (*) Mailman School ofPublic Health, Columbia University Medical Center, NewYork, NY, USA
Center forInnovation andOutcomes Research, NewYork Presbyterian Hospital/Columbia University Medical Center, NewYork, NY, USA e-mail: rpk2118@cumc.columbia.edu
cancer. These results helped to solidify our understanding of the step-wise development of colorectal cancer, involving both oncogene activation and loss of tumor suppressor gene activity.
B. The National Polyp Study, published in 1993,
provided further evidence for the progression of adenomatous polyps to colorectal cancer. In this study, patients who underwent screen­ing colonoscopy and polypectomy of histo­logically proven adenomatous polyps were compared to reference groups of patients for whom adenomatous polyps were not removed. The authors found that patients who underwent polypectomy had a lower-than­expected incidence of colorectal cancer when compared to the reference groups. This study underscored the importance of screening colonoscopy for the prevention of colorectal cancer.
C. Guidelines which suggest a colonoscopy
screening algorithm are published by the National Comprehensive Cancer Network (NCCN), last updated in 2016. Initial screen­ing for average risk individuals (no prior his­tory of adenomatous polyp or colorectal cancer, no family history of colorectal can­cer and no personal history of inammatory bowel disease) should start at 50 years of age. Individuals with any of the above con­ditions should be screened based on NCCN guideline suggestions. Special consideration
© Springer Nature Switzerland AG 2020 S. R. Steele etal. (eds.), Clinical Decision Making in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-65942-8_63
483
484
Fig. 63.1 Algorithm for colonic adenomatous polyps
S. A. Lee-Kong and P. R. Kiran
should be given to individuals in whom a high-risk colorectal cancer syndrome may exist. These categories include Lynch Syndrome, Hereditary Nonpolyposis Colorectal Cancer (HNPCC), classical or attenuated Familial Adenomatous Polyposis syndrome (FAP or aFAP), MUTYH­associated polyposis (MAP), Peutz-Jeghers syndrome, Juvenile polyposis syndrome, Serrated polyposis syndrome, Cowden syn­drome or Li-Fraumeni syndrome, who should be screened earlier. If an adenoma­tous polyp is found, complete removal should be performed. Intervals for repeat screening examinations depend on the pres­ence and number of adenomatous polyps found on the index colonoscopy, polyp size and the presence of advanced adenomas (high-grade dysplasia, sessile serrated his­tology, villous or tubulovillous histology).
If no adenomatous polyps are found at the index colonoscopy, repeat examination is rec­ommended in 10 years. Presence of 2 or fewer low-risk adenomatous polyps should prompt repeat examination in 5–10 years. Three or more adenomatous polyps, or pres­ence of advanced adenomas, should prompt a
repeat examination in 3years. Incomplete or piecemeal polypectomy should prompt repeat examination within 6months.
Patients with inammatory bowel disease are recommended screening colonoscopy 8–10 years after the onset of symptoms. Ongoing surveillance depends on disease activity in addition to endoscopic ndings. Individuals with a rst degree relative with a colorectal cancer diagnosed at less than age 60 years should have their index examina­tion at age 40, or 10 years earlier than the age of earliest CRC diagnosis in that rst­degree relative. Individuals with a rst­degree relative with an advanced adenoma should have their rst colonoscopy at either age 50 or at the age of the family member with the advanced adenoma, whichever is earlier.
D. Even after appropriately timed screening
colonoscopy, interval adenocarcinomas can occur in approximately 10.5% of patients. The majority of these interval lesions occur in the right colon. Theories as to the cause of this phenomenon include a worse bowel preparation in the right colon, biological dif­ferences in tumors of the right colon or an
63 Colonic Conditions: Adenomatous Polyps
485
increased proportion of at lesions in the right colon that may have been missed at screening colonoscopy. Meticulous inspec­tion behind mucosal folds and behind the ileocecal valve may help improve lesion detection.
E. During colonoscopy, polypectomy of small
lesions (less than 3 mm in diameter) can usually be achieved by use of a cold biopsy forceps. The instrument is passed through the working channel of the colonoscope and the lesion excised, either in its entirety with one pass or in “piecemeal” fashion. For this purpose, the authors prefer using a “jumbo” size forceps, as the jaws can accommodate more tissue and help ensure a complete pol­ypectomy. For larger polyps, biopsy forceps may not allow for complete polypectomy. In this situation, snare polypectomy may be necessary to ensure complete polyp exci­sion. This device is similarly passed via the working channel of the endoscope. The snare is opened and secured around the base of the polyp. Complete closure of the device amputates the lesion. Once complete, the polyp can be grasped and withdrawn by aide of a through- the- scope net or suctioned through the colonoscope and captured in a specimen trap. Submucosal injection can also be utilized to aide in excision of the polyp. An injectate such as normal saline, glycerol, or hyaluronic acid is injected in the submucosal plane beneath and around the polyp, “lifting” the lesion off the muscu­laris propria. This can allow a snare to be deployed around the lesion, and may also minimize the possibility of transmural injury to the bowel, particularly if cautery is used. There is no consensus as to which injectate provides the best results. Polyps that do not lift appropriately during injec­tion may indicate an invasive lesion, and complete polypectomy may not be possible. Prior attempts at polypectomy may also cause scarring within the lesion, precluding adequate lifting. For snare polypectomy, it is often helpful to position the lesion at the “5 o’clock” position on the screen, as this is
where the working channel port is. This should allow proper positioning of the snare.
F. Advances in exible endoscope technology
and equipment have provided the opportunity to improve adenoma detection rates. Advanced techniques are now available to safely remove adenomas, both small and large. In years past, patients discovered to have large adenomas considered too large to remove endoscopically were referred for sur­gical resection. Advanced endoscopic tech­niques, including endoscopic mucosal resection (EMR) and endoscopic submucosal dissection (ESD), have given endoscopists the opportunity to offer patients a minimally invasive approach to remove difcult colorec­tal polyps. While both techniques can be use­ful in avoiding major surgical resection for pre-malignant lesions, there are some key dif­ferences between the two. EMR is widely accepted for the resection of larger adenoma­tous polyps, however, larger lesions can be difcult to remove completely
9
. ESD can be used to improve completeness of resection (R0) and thereby decrease recurrence rates. A recent meta-analysis comparing EMR to ESD utilized data from 6 trials and pooled evalua­tion of 1642 adenomatous polyps. ESD was associated with higher en bloc resection and lower local recurrence. The complication rates were similar, however, ESD was more time consuming.
G. Advanced trans-anal approaches are also
available for patients with large rectal polyps. Transanal endoscopic microsurgery (TEMS) and transanal minimally invasive surgery (TAMIS) techniques have become more widespread and can allow for safe removal of accessible lesions. In a recent meta-analysis comparing TEMS to conventional transanal excision, TEMS was associated with a higher rate of negative margins, less specimen frag­mentation and lower recurrence rates, with no difference in overall complications. Recently, TAMIS has grown in popularity since its ini­tial description in 2010 by Atallah etal. While high quality data are still lacking, TAMIS has
486
S. A. Lee-Kong and P. R. Kiran
also shown promising results, comparable to TEMS 14 in terms of achieving negative mar­gins and minimizing polyp recurrence.
H. Surgical resection of the colon or rectum for
endoscopically unresectable adenomatous polyps, outside of transanal approaches, usu­ally requires partial colectomy. Patients deemed appropriate surgical candidates are offered abdominal surgery, which can be done in traditional open fashion or by utiliz­ing minimally invasive techniques. In gen­eral, traditional oncologic principles are followed during the resection, as larger ade­nomatous polyps can harbor invasive cancer. Some series report that for larger polyps between 1.5cm and 3.5cm in diameter, the risk of harboring an invasive cancer can range from 19 to 43%. Ensuring adequate lymphad­enectomy in this setting is important for can­cer staging.
I. Cancer within a polyp: Endoscopic vs surgical
resection.
Adenomatous polyps with foci of invasive cancer can be a management dilemma. The risk of lymphatic spread is directly correlated with the T-stage of the lesion. For peduncu­lated or sessile adenomatous polyps identied at colonoscopy, endoscopic resection can be entertained, if deemed appropriate by the endoscopist. Patients with pedunculated ade­nomatous polyps with foci of invasive cancer excised in 1 piece with clear margins, con­rmed to be T1in depth and with favorable histologic features (well or moderately differ­entiated, absent lymphovascular invasion) can safely observed without resection. For sessile lesions with the same above features, both observation and radial resection can be con­sidered appropriate treatment.
The Haggitt Classication system for pedunculated polyps with foci of invasive can­cer is useful to describe the level of invasion into the submucosa. Haggitt level 1 lesions have the component of adenocarcinoma lim­ited to the head of the polyp. Level 2 lesions have the adenocarcinoma extend to the neck of the polyp. Level 3 lesions have cancer extension to the stalk of the polyp, and in level
4 lesions extend beyond the stalk, but still lim­ited to the submucosa. Haggitt levels 1–3 are associated with a very low rate of lymph node metastasis, and these lesions can be safely managed with endoscopic polypectomy.

Suggested Reading

Atallah S, Albert M, Larach S. Transanal minimally
invasive surgery: a giant leap forward. Surg Endosc. 2010;24:2200–5.
Białek A, Wiechowska-Kozłowska A, Pertkiewicz J,
Karpińska K, Marlicz W, Milkiewicz P, Starzyńska T. Endoscopic submucosal dissection for the treat­ment of neoplastic lesions in the gastrointestinal tract. World J Gastroenterol. 2013;19:1953–61.
Clancy C, Burke JP, Albert MR, O’Connell PR, Winter
DC.Transanal endoscopic microsurgery versus stan­dard transanal excision for the removal of rectal neo­plasms: a systematic review and meta-analysis. Dis Colon Rectum. 2015;58:254–61.
Draganov PV, Chang MN, Alkhasawneh A, et al.
Randomized, controlled trial of standard, large­capacity versus jumbo biopsy forceps for polypec­tomy of small, sessile, colorectal polyps. Gastrointest Endosc. 2012;75(1):118–26.
Haggitt RC, Glotzbach RE, Soffer EE, Wruble
LD.Prognostic factors in colorectal carcinomas aris­ing in adenomas: implications for lesions removed by endoscopic polypectomy. Gastroenterology. 1985;89(2):328–36.
Keller DS, Haas EM. Transanal minimally inva-
sive surgery: State of the art. J Gastrointest Surg. 2016;20:463–9.
Lockhart-Mummery JP, Dukes C. The precancerous
changes in the rectum and colon. Surg Gynecol Obstet. 1927;36:591–6.
National Comprehensive Cancer Network. Colorectal
cancer screening (Version1.2015). www.nccn.org/pro-
fessionals/physicians_gls/PDF/colorectal_screening. pdf. Accessed July 2016.
National Comprehensive Cancer Network. Colon cancer
(Version 1.2017). https://www.nccn.org/professionals/
physician_gls/pdf/colon.pdf. Accessed Dec 2016.
Nivatvongs S. Surgical management of malig-
nant colorectal polyps. Surg Clin North Am. 2002;82:959–66.
Nusko G, Mansmann U, Partzsch U, Altendorf-Hofmann
A, Groitl H, Wittekind C, Ell C, Hahn EG.Invasive carcinoma in colorectal adenomas: multivariate analy­sis of patient and adenoma characteristics. Endoscopy. 1997;29:626–31.
Shergill AK, Conners EE, McQuaid KR, Epstein S, Ryan
JC, Shah JN, Inadomi J, Somsouk M. Protective association of colonoscopy against proximal and distal colon cancer and patterns of interval cancer. Gastrointest Endosc. 2015;82:529–37.
63 Colonic Conditions: Adenomatous Polyps
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Colon Cancer Surgical Therapy

LameeseTabaja, YasirAkmal, andMaherA.Abbas
64
Refer toAlgorithm inFig. 64.1
A. The colon occupies portions of the retroperi-
toneal and intraperitoneal abdominal spaces, in close proximity to multiple solid organs and the small bowel. The ascending and descending colon are retroperitoneal, while the transverse colon is intraperitoneal. The sigmoid colon ends where the taenia con­verge to form the rectum.
B. The entire right colon to the junction of the
middle and distal third of the transverse colon are supplied by the right colic and the ileo-colic arteries (Fig. 64.2), which are branches of the superior mesenteric artery. The middle colic artery supplies the majority of the transverse colon. The arterial supply of the distal transverse and left colon down to the lower rectum are supplied by the left colic and sigmoid arteries which are branches of the inferior mesenteric artery. These branches anastomose with the left branch of the middle colic artery to form part of the marginal artery of Drummond. The marginal artery of Drummond and the arc of Riolan provide the collateral blood circulation and typically the blood supply of the transverse
L. Tabaja (*) · Y. Akmal · M. A. Abbas Department of Colon and Rectal Surgery, Digestive Disease Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates e-mail: TabajaL@clevelandclinicabudhabi.ae
colon is excellent, as long as the marginal artery is not damaged. Variability in the arte­rial anastomoses occurs, which is an impor­tant point when performing a segmental resection. The two most tenuous sites, “watershed areas”, are the splenic exure (Grifth’s point) and the distal descending colon (Sudeck’s point). The venous and lym­phatic drainage of the colon tends to parallel the arterial supply (Figs.64.3 and 64.4). For the right and left colon, the venous drainage is through the superior and inferior mesen­teric veins, respectively.
C. The extent of resection is based on the blood
supply that drains the tumor-bearing seg­ment of the colon. It is recommended that the proximal and distal margins are a mini­mum of 5cm. The mesentery of the affected segment should be removed en bloc with the major feeding vessel(s) and the dependent lymphatic drainage. Any malignant­appearing lymph nodes (LNs) outside the boundaries of the resection should also be removed if possible. Standard ligation of the feeding vessel at the origin is recommended by the American Society of Colon and Rectal Surgeons (ASCRS). Furthermore, one large study suggests a higher overall survival and lower recurrence rate when high vascular ligation is performed for Stages II and III (i.e., Dukes B and C) colorectal tumors. A minimum of 12 LNs should be identied and evaluated from the resected colon cancer
© Springer Nature Switzerland AG 2020 S. R. Steele etal. (eds.), Clinical Decision Making in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-65942-8_64
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