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Download MBBS Surgery Presentations 7 Benign And Malignant Tumors of The Rectum Lecture Notes

Download MBBS (Bachelor of Medicine, Bachelor of Surgery) 1st Year, 2nd Year, 3rd Year and Final year Surgery 7 Benign And Malignant Tumors of The Rectum PPT-Powerpoint Presentations and lecture notes

This post was last modified on 08 April 2022

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1 . Benign tumors

2. Malignant tumors
Benign rectal tumors

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The most frequent are polyps.

Polyp is a localised elevated lesion arising from an epithelial surface.

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Polyp - adenoma : 90%

- other ( inflammatory, hyperplastic etc. ) : 10%

2 types of adenoma : tubular ( pedunculated ) 20%

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villous ( sessile ) 80%

Neoplastic Polyps

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? These lesions are dysplastic
? The risk of malignant degeneration is related to both the size

and type of polyp.

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? Tubular adenomas are associated with malignancy in only 5% of

cases

? Villous adenomas may harbor cancer in up to 40%

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? Tubulovillous adenomas are at intermediate risk (22%)
? Invasive carcinomas are rare in polyps smaller than 1 cm
? Polyps may be pedunculated or sessile
? Pedunculated polyps : Colonoscopic snare excision
? Sessile polyp: Transanal operative excision

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? The site of sessile polypectomies should be marked by

injection of methylene blue or India ink to:

? guide follow-up colonoscopy sessions

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? ensure that the polyp has been completely removed
? facilitate identification of the involved bowel segment should

operative resection be necessary

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? Colectomy is reserved for

? large, flat lesions
? focus of invasive cancer is confirmed in the specimen.

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? These patients may be ideal candidates for laparoscopic

colectomy

Hamartomatous Polyps (Juvenile Polyps)

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? Not usually premalignant
? These lesions are the characteristic polyps of childhood

but may occur at any age.

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? Bleeding is a common symptom and intussusception

and/or obstruction may occur.

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? Because the gross appearance of these polyps is

identical to adenomatous polyps, these lesions should
also be treated by polypectomy.
? Familial juvenile polyposis

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? Autosomal dominant disorder
? Annual screening :between the ages of 10 and 12 years.

Treatment is surgical and depends in part upon the degree of

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rectal involvement.

? If the rectum is relatively spared, a total abdominal colectomy

with ileorectal anastomosis may be performed

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? If the rectum is carpeted with polyps, total proctocolectomy is the

more appropriate operation

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Peutz-Jeghers syndrome
? polyposis of the smal intestine, and lesser extent, polyposis of the colon

and rectum.

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? Characteristic melanin spots are often noted on the buccal mucosa and

lips of these patients.

? Not at significant risk for malignant degeneration.

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? Carcinoma may occasional y develop.
? Because the entire length of the gastrointestinal tract may be affected,

surgery is reserved for symptoms such as obstruction or bleeding or in
whom polyps develop adenomatous features.

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? Screening consists of a baseline colonoscopy and upper endoscopy at

age 20 years, followed by annual flexible sigmoidoscopy thereafter.
Cronkite-Canada syndrome

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? Gastrointestinal polyposis in association with alopecia, cutaneous

pigmentation, and atrophy of the fingernails and toenails.

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? Diarrhea is a prominent symptom, and vomiting, malabsorption, and

protein-losing enteropathy may occur

? Surgery is reserved for complications such as obstruction

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Cowden's syndrome

Autosomal dominant disorder
hamartomas of all three embryonal cell layers

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Facial trichilemmomas, breast cancer, thyroid disease, and

gastrointestinal polyps are typical of the syndrome.

Treatment is otherwise based upon symptoms

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Inflammatory Polyps (Pseudopolyps)

? Not premalignant

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? Microscopic examination shows islands of normal,

regenerating mucosa (the polyp) surrounded by areas of

mucosal loss.

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? Polyposis may be extensive, especially in patients with severe

colitis, and may mimic familial adenomatous polyposis.
Familial Adenomatous Polyposis

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? Autosomal dominant condition
? 1% of al colorectal adenocarcinomas.
? The genetic abnormality in FAP is a mutation in the APC gene, located

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on chromosome 5q.

? most patients with FAP wil have a known family history of the disease,

up to 25% present without other affected family members.

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? Clinical y, patients develop hundreds to thousands of adenomatous

polyps shortly after puberty.

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? The lifetime risk of colorectal cancer in FAP patients approaches 100%

by age 50 years.

? Flexible sigmoidoscopy of first-degree relatives of FAP patients

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beginning at age 10 to 15 years

? APC gene testing may be used to screen family members

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? Positive: annual flexible sigmoidoscopy beginning at age 10 to

15 years

? Negative: screening starting at age 50 years

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? FAP patients are also at risk for the development of adenomas

anywhere in the gastrointestinal tract, particularly in the duodenum.

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? Periampul ary carcinoma is a particular concern.

? Upper endoscopy is therefore recommended for surveil ance every

1 to 3 years beginning at age 25 to 30 years

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? Treatment is surgical
? Three operative procedures can be considered

? total proctocolectomy with either an end (Brooke's)

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ileostomy or continent (Kock's) ileostomy

? total abdominal colectomy with ileorectal anastomosis

? restorative proctocolectomy with ileal pouch?anal

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anastomosis with or without a temporary ileostomy

Hereditary Nonpolyposis Colon Cancer

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(Lynch's Syndrome)

? more common than FAP
? extremely rare (1 to 3%)
? The genetic defects associated with HNPCC arise from errors in

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mismatch repair and study of this syndrome has elucidated many

of the details of the RER pathway.

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? an autosomal dominant pattern
? development of colorectal carcinoma at an early age
? The risk of synchronous or metachronous colorectal carcinoma is

40%. HNPCC may also be associated with extracolonic

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malignancies, including endometrial, ovarian, pancreas, stomach,

small bowel, biliary, and urinary tract carcinomas.
? Screening colonoscopy: recommended annual y for at-risk patients

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beginning at either age 20 to 25 years or 10 years younger than the

youngest age at diagnosis in the family, whichever comes first.

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? Because there is a 40% risk of developing a second colon cancer,

total colectomy with ileorectal anastomosis is recommended once

adenomas or a colon carcinoma is diagnosed, or if prophylactic

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colectomy is decided upon.

? Annual proctoscopy is necessary because the risk of developing

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rectal cancer remains high.

? Similarly, prophylactic hysterectomy and bilateral salpingo-

oophorectomy should be considered in women who have

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completed childbearing.

Familial Colorectal Cancer

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? Nonsyndromic familial colorectal cancer accounts for 10

to 15% of patients with colorectal cancer.

? Screening colonoscopy is recommended every 5 years

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beginning at age 40 years or beginning 10 years before

the age of the earliest diagnosed patient in the pedigree.

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? No specific genetic abnormalities are associated with

familial colorectal cancer, the defects found in either the

LOH pathway or RER pathway may be present in these

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patients.
Adenoma Carcinoma sequence

Rectal carcinoma

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Factors associated with Factors associated with

increased risk for CRC

decreased risk for CRC

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? Lack of physical activity ? MVI containing folic acid

? Consumption of red meat ? ASA and other NSAID's

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? Obesity

? Post menopausal HRT

? Cigarette smoking

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? Ca supplementation

? Alcohol use

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? Selenium
? Consumption of fruits,

vegetables and fiber

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? Rectal cancer ( adenocarcinoma ) arising from the epithelial cells

of the rectal mucosa.

? 50% of all colorectal tumors are located in the rectum

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? The incidence rate rises dramatically during the fifth decade of life

? Increased risk of colorectal cancer associated with cigarette

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smoking is dependent on the molecular characteristics of the

tumor as defined by APC mutation and hMLH1 expression status
Clinical Presentation

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? Rectal bleeding
? Changes in bowel habits
? Increased frequency of defecation, decreased caliber of the

stools, mucus with stools, or mucous diarrhea

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? Sense of fullness,tenesmus,increased straining during defecation.
? Sacral or deep pelvic pain
? Anal pain (occurs when low rectal cancer invades the anal canal)
? Incontinence supervenes when the anal sphincter is involved

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? Liver is the most frequent site of metastasis, followed by the

lung, retroperitoneum, ovary, peritoneal cavity, and rarely the

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adrenal glands
Physical examination

Digital rectal examination

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? Feel for a mass, assess its location and mobility

? Depth of invasion and whether the tumor is tethered or fixed

? Pelvic examination in women

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? Prostate assessment in men

A weak or incompetent sphincter may favor a colostomy.

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? Rigid proctosigmoidoscopic examination

? If not obstructed, patients with rectal cancer should

have a preoperative double-contrast barium enema

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or preferably a colonoscopy to assess for

synchronous colon cancer (2% to 9%)

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Endorectal ultrasound

? Depth of tumor invasion into the rectal wall

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? Nodal enlargement

? Malignant nodes are differentiated from reactive nodes by

being hypoechoic, hypervascular, and irregular

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? CECT scan abdomen &pelvis
? MRI for patients with locally advanced and recurrent rectal

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cancer requiring an exenterative procedure.

? Plain chest radiograph
? Laboratory studies
? Carcinoembryonic antigen (CEA) level

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Up to 95% of patients with advanced hepatic metastasis will

have a CEA level above 20 ng/mL.

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Staging
Management

Surgical excision:

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? Surgical resection of affected bowel with clear margins,

along with the adjacent mesentery and at least 12 regional

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nodes

? For rectal tumors, total mesorectal excision with a distal

surgical margin of at least 2 cm is recommended

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? For tumors that are located within 6 cm of the anal verge,

or involve the anal sphincter, wide surgical resection with

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abdomino-perineal resection and permanent colostomy is

recommended

? Local excision, for pal iative treatment or simple polyp

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removal

Radiation therapy:

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? Postoperative radiation, with or without

chemotherapy, significantly reduces local recurrence

rates

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? Common regimen incorporates infusional 5-

fluorouracil (5-FU) as a radiosensitizer to boost the

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efficacy of pelvic radiation

? Administered as 45 to 55 Gy over 5 weeks
Systemic Chemotherapy
? 5-FU has been the mainstay of systemic

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chemotherapy for CRC

? Capecitabine was approved in 2001 as first-line

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therapy for metastatic CRC

? Irinotecan (Camptosar), Oxaliplatin (Eloxatin),

Bevacizumab, Cetuximab

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Carcinoid Tumors

? 25% of these tumors are found in the rectum.
? Most small rectal carcinoids are benign, and overall survival is

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greater than 80%.

? >60% of tumors greater than 2 cm in diameter are associated

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with distant metastases.

? less likely to secrete vasoactive substances than carcinoids in

other locations, and carcinoid syndrome is uncommon in the

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absence of hepatic metastases.

? Small carcinoids can be locally resected, either transanally or

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using transanal endoscopic microsurgery.

? Larger tumors or tumors with obvious invasion into the

muscularis require more radical surgery.

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