Colonic Structure<\/a><\/li><\/ul><\/nav><\/div>\n\nCaecum<\/strong><\/p>\n\n- 7.5 cm in both length and breadth<\/li>\n
- Blind pouch<\/li>\n
- Completely covered by peritoneum except posterior surface<\/li>\n
- Mobile<\/li>\n<\/ul>\n
Caecum Diseases:\u00a0<\/strong><\/p>\n\n- Carcinoma<\/li>\n
- Tuberculosis<\/li>\n
- Amoebic typhlitis<\/li>\n
- Intussusception<\/li>\n
- Volvulus\u2014rare<\/li>\n<\/ul>\n
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Ascending Colon (15 cm Long)<\/strong><\/p>\n\n- Caecum continues as ascending colon.<\/li>\n
- Covered by peritoneum in front and on both sides.<\/li>\n
- In 25% of patients, it has a mesentery.<\/li>\n
- The right paracolic gutter is deep on the lateral aspect of ascending colon\u2014space for paracolic abscess in cases of perforation peritonitis.<\/li>\n<\/ul>\n
Transverse Colon (50 cm Long)<\/strong><\/p>\n\n- The most mobile part of large intestine.<\/li>\n
- It is suspended by transverse mesocolon, loops down and is adherent to the posterior wall of the omental bursa.<\/li>\n<\/ul>\n
Transverse Colon Diseases:<\/strong><\/p>\n\n- Cancer<\/li>\n
- Ulcerative colitis<\/li>\n<\/ul>\n
Descending Colon (25 cm Long)<\/strong><\/p>\n\n- Continues as sigmoid colon<\/li>\n
- Retroperitoneal (like ascending colon)<\/li>\n
- Also has a paracolic gutter<\/li>\n<\/ul>\n
Sigmoid (40 cm Long)<\/strong><\/p>\n\n- S-shaped<\/li>\n
- Ends as a rectosigmoid junction where taenia coli ends.<\/li>\n<\/ul>\n
Sigmoid<\/strong> Diseases:<\/strong><\/p>\n\n- Volvulus<\/li>\n
- Diverticulosis<\/li>\n
- Cancer<\/li>\n<\/ul>\n
Right Colon: <\/strong>The big\u00a0and hepatic flexure is broad.<\/p>\nLeft Colon<\/strong><\/p>\n\n- Small and splenic flexure is acute. Hence, ischaemic colitis commonly affects splenic flexure<\/li>\n
- Splenic flexure is deeply situated. Therefore, malignancy in this area can be easily missed.<\/li>\n<\/ul>\n
Comparison between Right and Left colon:<\/strong><\/p>\n
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Muscle Coat<\/strong><\/p>\n\n- Outer longitudinal muscle is arranged in the form of three strips called taenia coli.<\/li>\n
- All three join at the rectosigmoid junction and form a complete longitudinal layer of the rectum. These three taenia coli converge at the base of the appendix.<\/li>\n
- This is an important method to localise the appendix. Inner circular muscle coalesces distally to form an internal anal sphincter. No taenia over the rectum.<\/li>\n<\/ul>\n
Recognise large intestine by:<\/strong><\/p>\n\n- Taenia coli<\/li>\n
- Omental appendices\u2014appendicular epiploic ae<\/li>\n
- Haustrations<\/li>\n
- Large diameter (calibre)<\/li>\n<\/ul>\n
Names of three Taenia coli:\u00a0<\/strong><\/p>\n\n- Mesocolic:<\/strong> Transverse colon and sigmoid colon are attached by this.<\/li>\n
- Omental:<\/strong> To which omental appendices attach.<\/li>\n
- Libera (free):<\/strong> Nothing is attached.<\/li>\n<\/ol>\n
Colorectal Arterial Supply<\/strong><\/p>\n1. Superior mesenteric artery:<\/strong><\/p>\nA branch of the abdominal aorta arises at the level of the first lumbar vertebra (L1). It supplies the entire small bowel and the right colon up to the proximal 2\/3rds of the transverse colon.<\/p>\n
Branches of the superior mesenteric artery (SMA) supplying the colon are:<\/strong><\/p>\n\n- Middle colic artery:<\/strong>\u00a0 The middle colic artery supplies ascending colon, hepatic flexure and transverse colon. It divides into right and left branches.<\/li>\n
- The right colic artery supplies the right colon.<\/li>\n
- The ileocolic artery supplies the terminal ileum and ascending colon. It divides into anterior and posterior caecal branches and supplies the caecum and appendix through the appendicular artery.<\/li>\n<\/ul>\n
Comparison Between Right And Left Colon:<\/strong><\/p>\n
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2. The inferior mesenteric artery (IMA):<\/strong> A branch of the abdominal aorta arising at the level of L3, supplies the left colon up to the mucocutaneous junction at the lower end of the anal canal (Hilton\u2019s line).<\/p>\n Its branches are:<\/strong><\/p>\n\n- Left colic artery:<\/strong> Left colic artery which anastomoses with branches of the middle colic artery. It divides into upper and lower branches supplying the descending colon.<\/li>\n
- Three sigmoidal branches supply the sigmoid colon:<\/strong> The narrow point of blood supply between the first sigmoidal artery and left coelic artery is called Sudeck\u2019s point.<\/li>\n
- \u00a0Superior haemorrhoidal artery (rectal):\u00a0<\/strong>\n
\n- The anastomotic branches form the marginal artery of Drummond, which is relatively narrow in the region of splenic flexure (another reason for the development of ischaemia).<\/li>\n
- That narrow point is called Griffith\u2019s point.<\/li>\n
- The Arc of Riolan is the anastomotic arcade formed between branches of IMA and SMA.<\/li>\n<\/ul>\n<\/li>\n<\/ol>\n
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Colorectal Venous Supply<\/strong><\/p>\n\n- Follows the corresponding artery and empties into superior and inferior mesenteric veins, ultimately draining into the portal vein.<\/li>\n
- Thus, if the colorectal area gets infected secondary to inflammatory conditions or after a surgical procedure, the infection can easily spread to the portal vein and result in portal pyaemia.<\/li>\n<\/ul>\n
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Lymphatic Drainage<\/strong><\/p>\n\n- N1:<\/strong> Epicolic and paracolic nodes are the first to get involved.<\/li>\n
- N2:<\/strong> Nodes at the origin of ileocolic and middle colic arteries\u2014intermediate nodes.<\/li>\n
- N3: Nodes at the origin of superior and inferior mesenteric arteries. They are involved in approximately 50% of the patients with carcinoma colon at presentation to the hospital. These are called principal nodes.<\/li>\n<\/ol>\n
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Colorectal Nerve Supply<\/strong><\/p>\n\n- Sympathetic (inhibitory) arise from T10\u2013T12 and L1\u2013L<\/li>\n
- Parasympathetic (stimulation).\n
\n- The vagus nerve supplies the right and transverse colon.<\/li>\n
- Sacral nerves (S2\u2013S4 which form nervi erigentes) supply the distal colon, i.e. splenic flexure onwards.<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n
Colorectal Significance:\u00a0<\/strong><\/p>\n\n- Colonic pseudo-obstruction starts from splenic flexure.<\/li>\n
- The transition zone of vagal supply to sacral nerve supply.<\/li>\n<\/ul>\n
<\/span>Tumours Of The Large Intestine<\/span><\/h2>\nBenign tumours are usually referred to as polyps, which means elevated from the surface. Adenomatous polyps have got malignant potential. A few criteria have been incorporated into a system when malignancy develops in the polyp.<\/p>\n
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\n- It takes into consideration of level of invasion.<\/li>\n
- Level 1:<\/strong> In this, carcinoma is limited to the top of the polyp. From the mucosa, it is invading through muscularis mucosa into the submucosa.<\/li>\n
- Level 2:<\/strong> Carcinoma at the junction of head and stalk.<\/li>\n
- Level 3:<\/strong> Carcinoma confined to anywhere in the stalk.<\/li>\n
- Level 4:<\/strong> Infiltration into submucosa.<\/li>\n<\/ul>\n
<\/span>Adenomatous Polyp<\/span><\/h2>\n\n- It may be a villous adenoma which is a flat lesion or a tubular adenoma having a pedicle. Tubular is more common.<\/li>\n
- They give rise to bleeding, mucus diarrhoea and hypokalaemia.<\/li>\n
- They can be single or multiple.<\/li>\n
- They are dysplastic.<\/li>\n
- They are premalignant and the risk of malignancy is greater with an increase in the size of the adenoma.<\/li>\n
- They can be removed with the colonoscope\u2014 polypectomy.<\/li>\n
- The malignant potential of villous adenoma is more than tubular adenoma.<\/li>\n
- Adenoma less than 1 cm\u2014the risk of malignancy is 1%; 1\u20132 cm is 10%; >2 cm is 30%.<\/li>\n
- Most of the neoplastic polyps occur in elderly patients(>50 years).<\/li>\n
- Most of them are pedunculated.<\/li>\n
- Most pedunculated polyps are removed by colonoscopic snaring.<\/li>\n
- Adenomas larger than 5 mm in diameter carry a risk of malignant potential.<\/li>\n
- The more the polyps, the more chances of synchronous carcinoma.<\/li>\n
- Flat adenomas also carry malignant potential.<\/li>\n<\/ul>\n
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Symptoms and signs of polyps:<\/strong> Bleeding per rectum is the most common symptom. Fresh bleeding is seen in rectal polyps. Typically, it is painless. It is intermittent. If it is associated with the change of bowel habits it is probably a malignant change. These changes include mucus discharge, tenesmus, and sometimes constipation. In children, polyps may project outside the anus. In such cases, it has to be distinguished from a prolapsed rectum.<\/p>\nAdenomatous Polyp Treatment:\u00a0<\/strong><\/p>\n\n- Colonoscopy and polypectomy is the standard treatment.<\/li>\n
- If the specimen shows invasive carcinoma, radical surgery needs to be done.<\/li>\n<\/ul>\n
<\/span>Hamartomatous Polyp (Juvenile Polyp)<\/span><\/h2>\n\n- This can occur in the colon as in Peutz-Jeghers syndrome. The risk of malignancy is very limited.<\/li>\n
- Symptomatic polyps need to be treated.<\/li>\n
- Juvenile polyps are usually single and occur in children. They give rise to bleeding and are easily resected. They do not have malignant potential.<\/li>\n<\/ul>\n
<\/span>Familial Polyposis Coli (Fpc) Or Familial Adenomatous Polyposis (Fap)<\/span><\/h2>\n\n- FAP is a genetic disorder inherited as a Mendelian dominant. The gene APC (adenomatous polyposis coli) is located on the short arm of chromosome 5. Prevalence: 1 in 10,000. It is clinically defined by the presence of more than 100 colorectal adenomas.<\/li>\n
- It is transmitted from both sexes. The incidence is same in either sex.<\/li>\n<\/ul>\n
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\n- When it is associated with desmoid tumour, craniofacial osteomas, epidermoid cysts, and congenital hypertrophy of retinal pigment epithelium, it is described as Gardner\u2019s syndrome.<\/li>\n
- When familial polyposis coli is associated with central nervous system tumour and glioblastoma, it is called Turcot\u2019s syndrome.<\/li>\n
- 50% of them have benign gastric polyps and 90% of them have duodenal polyps.<\/li>\n<\/ul>\n
\u00a0FAP <\/strong>Clinical Features:\u00a0<\/strong><\/p>\n\n- Runs in families; other members of the family are affected.<\/li>\n
- Manifests at the age of 20 in the form of blood and mucus in the stool, loose stools, etc. It produces crampy lower abdominal pain.<\/li>\n
- Anaemia, weight loss and protein malnutrition occur slowly.<\/li>\n
- The mean age of development of carcinoma is 29 years.<\/li>\n<\/ul>\n
FAP Complications: <\/strong>Malignancy (100% risk)<\/p>\nFamily Polyposis Coli:<\/strong><\/p>\n\n- Polyps are more than 100 (colorectal adenomas).<\/li>\n
- Other mesodermal tumours\u2014desmoid tumours, osteoma, and epidermoid cysts can be present (Gardner\u2019s syndrome).<\/li>\n
- Large bowel is predominantly involved.<\/li>\n
- Year of development of carcinoma\u2014mean age 39 years.<\/li>\n
- Polyposis gene\u2014autosomal dominant APC gene.<\/li>\n
- Other syndrome\u2014Turcot<\/li>\n
- Sigmoidoscopy from the age of 15 at intervals is the investigation of choice.<\/li>\n
- I leoanal anastomosis with pouch\u2014restorative proctocolectomy\u2014advisable above age of 30.<\/li>\n
- Surgery is the only means of preventing colonic cancer.<\/li>\n
- Remember as POLYPOSI<\/strong><\/li>\n<\/ul>\n
FAP Treatment:\u00a0<\/strong><\/p>\n\n- NSAID:<\/strong> Sulindac 300 mg, twice a day and aspirin 325 mg once a day have been found to decrease the size of polyps.<\/li>\n
- Patients with FAP who are above the age of 30 have high chances of having a carcinoma in the colon. Hence, even when there is no malignancy, surgery is advisable.<\/li>\n<\/ul>\n
Types of Surgery:<\/strong><\/p>\n\n- Many patients do not like ileostomy. Hence, a subtotal colectomy with ileorectal anastomosis can be done.<\/li>\n
- This is done provided that the rectum is examined frequently and endoscopic snaring of the polyps is done regularly, especially in a young patient.<\/li>\n
- Restorative proctocolectomy with ileoanal anastomosis by using a pouch is another alternative.<\/li>\n
- However, it is a major surgical procedure and should be undertaken only by an experienced surgeon.<\/li>\n<\/ul>\n
Screening: <\/strong>Starts from the age of 10\u201312 years, repeat every 1\u20132 years.<\/p>\n<\/span>Metaplastic Polyp<\/span><\/h2>\nAlso called hyperplastic nodules. They are of viral aetiology. They do not have malignant potential.<\/p>\n
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<\/span>Hereditary Nonpolyposis Colorectal Cancer (Hnpcc)<\/span><\/h2>\n\n- Autosomal dominant, no polyps<\/li>\n
- Lynch\u2019s syndrome 1: Site-specific colorectal cancer.<\/li>\n
- Lynch\u2019s syndrome 2: Cancer family syndrome\u2014they have extracolonic cancers such as endometrial cancer, ovarian cancer, transitional cell cancer, etc.<\/li>\n
- The lifetime risk of developing colorectal cancer is 80%.<\/li>\n
- Synchronous carcinoma means more than one cancer at the time of diagnosis. Metachronous carcinoma which means the appearance of a second carcinoma after 6 months can occur here.<\/li>\n<\/ul>\n
Diagnostic Criteria (Amsterdam Criteria II):<\/strong><\/p>\n\n- At least 3 members in a family should have colorectal cancer\u2014two of whom are first-degree relatives.<\/li>\n
- At least two consecutive generations.<\/li>\n
- At least one relative should have had colorectal cancer by less than 50 years of age.<\/li>\n
- Exclusion of FAP.<\/li>\n<\/ul>\n
Screening: <\/strong>Increased incidence of proximal colonic cancer.<\/p>\n<\/span>Examination Of Colon<\/span><\/h2>\nAnoproctoscopy:<\/strong> One can examine up to 10\u201312 cm of the anal canal and rectum. Rubber band ligation (for piles) and polypectomy can be done with this instrument.<\/p>\nFlexible sigmoidoscopy:<\/strong><\/p>\nThe scope measures about 60 cm in length. One can easily reach up to splenic flexure.<\/p>\n
\n- A bowel wash or an enema is given before the procedure.<\/li>\n
- No sedation is required.<\/li>\n<\/ul>\n
Fibreoptic colonoscopy:<\/strong> Fibreoptic colonoscopy can assess the entire colon. It is 100\u2013160 cm in length.<\/p>\n