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- •Foreword
- •Preface
- •Contents
- •Contributors
- •Editors
- •Authors
- •Anal Canal Epithelium
- •External Anal Sphincter
- •Hemorrhoids
- •Perineal Body
- •Pelvic Floor Muscles
- •Puborectalis Muscle
- •Iliococcygeus Muscle
- •Pubococcygeus Muscle
- •Mesorectum
- •Presacral Fascia
- •Retrosacral Fascia
- •Waldeyer’s Fascia
- •Denonvilliers’ Fascia
- •Lateral Ligaments
- •Anorectal Spaces
- •Perianal Space
- •Intersphincteric Space
- •Submucous Space
- •Ischioanal/Ischiorectal Space
- •Supralevator Space
- •Retrorectal Space
- •Internal Anal Sphincter
- •Conjoined Longitudinal Muscle
- •Rectal Blood Supply
- •Superior Rectal Artery
- •Middle Rectal Artery
- •Inferior Rectal Artery
- •Cecum
- •The Appendix
- •Ascending Colon
- •Transverse Colon
- •Descending Colon
- •Sigmoid Colon
- •Rectosigmoid Junction
- •Blood Supply
- •Superior Mesenteric Artery
- •Inferior Mesenteric Artery
- •Venous Drainage
- •Lymphatic Drainage
- •Nervous Innervation
- •Embryology
- •Midgut Rotation
- •Non-rotation
- •Malrotation
- •Reversed Rotation
- •Omphalocele
- •Internal Hernias
- •Proximal Colon Duplication
- •Meckel’s Diverticulum
- •Hirschsprung’s Disease
- •Anorectal Malformations
- •Anal Stenosis
- •Membranous Atresia
- •Anal Agenesis
- •Anorectal Agenesis
- •Rectal Atresia or “High Atresia”
- •Persistent Cloaca
- •References
- •2: Colonic Physiology
- •Embryology
- •Colonic Anatomy
- •Introduction
- •Colonic Wall Anatomy
- •Epithelial Types
- •Sodium
- •Potassium
- •Aldosterone
- •Short-Chain Fatty Acid Absorption
- •Vitamin K Absorption
- •Colonic Innervation
- •Pain
- •Colonic Motility
- •Microbiome
- •Conclusion
- •References
- •3: Anorectal Physiology
- •Introduction
- •Anatomy
- •Physiology
- •Normal Continence
- •Patient Positioning
- •Digital Rectal Examination
- •Anoscopy
- •Proctoscopy
- •Endoanal/Endorectal Ultrasound
- •Normal Defecation
- •Physiologic Testing
- •Anal Manometry
- •Pudendal Nerve Terminal Motor Latency
- •Defecography
- •Functional Anorectal Disorders
- •Fecal Incontinence
- •Anorectal Pain
- •Urogynecological Considerations
- •References
- •4: Endoscopy
- •Introduction
- •Anorectal Examination
- •Flexible Endoscopy Techniques
- •Torque
- •Dithering/Jiggle
- •Air Aspiration
- •Slide-By
- •Flexible Sigmoidoscopy
- •Colonoscopy
- •Bowel Preparation
- •Special Considerations
- •Anticoagulated Patient
- •Sedation
- •Instrumentation
- •Colonoscopy Technique
- •Alternative Techniques
- •Chromoendoscopy
- •Narrow Band Imaging
- •Full-Spectrum Endoscopy
- •Changing Patient Position
- •Abdominal Pressure
- •Incomplete Colonoscopy
- •Complications
- •Procedural Complications
- •Perforation
- •Bleeding
- •Post-polypectomy Syndrome
- •Splenic Injury
- •Infectious Complications
- •The Endoscopy Unit
- •Endoscope Processing
- •Quality Measures
- •Withdrawal Time
- •Adenoma Detection Rate
- •Leasing vs Purchasing Endoscopy Equipment
- •Summary
- •References
- •Introduction
- •Forceps
- •Snare
- •Lifting
- •Endoscopic Mucosal Resection
- •Clip
- •Underwater EMR
- •Endoscopic Submucosal Dissection
- •ESD Complications
- •ESD Technique
- •Postoperative Care
- •Endoscopic Suturing
- •Stabilization Platforms
- •Colonic Stenting
- •Stenting Technique
- •Stenting Anastomotic Leaks
- •Conclusion
- •References
- •Abdominal Surgery
- •Anorectal Surgery
- •Preoperative Testing
- •Laboratory Studies
- •Electrocardiogram
- •Chest X-Ray
- •Advanced Diagnostic Imaging
- •Cardiac Evaluation
- •Initial Workup
- •Additional Testing
- •Preoperative Anticoagulation
- •Coronary Stent Management
- •Bridging
- •AICD/Management
- •Pulmonary Assessment
- •Perioperative Steroid Management
- •Diabetes
- •Obesity
- •Malnutrition
- •Solid Organ Transplant Recipients
- •Substance Abuse
- •Alcohol
- •Tobacco
- •Opioids
- •Other Illicit Drugs
- •Immunosuppressive Agents
- •Assessing Frailty
- •Complete Geriatric Assessment
- •Frailty Scores
- •Prehabilitation
- •Exercise
- •Nutrition
- •Psychosocial Therapy
- •Outcomes
- •Conclusion
- •References
- •Enhanced Recovery Models
- •Education
- •Preoperative Optimization
- •Smoking Cessation
- •Preoperative Nutrition
- •Preoperative Anemia
- •Perioperative Hyperglycemia
- •Bowel Preparation
- •In-hospital Preoperative Enhanced Recovery Elements
- •Multimodal Analgesia (MMA)
- •Intraoperative Enhanced Recovery Elements
- •Multimodal Analgesia
- •Intentional Fluid Management
- •Minimally Invasive Surgical Approaches
- •Postoperative Enhanced Recovery
- •Multimodal Analgesia
- •Standard Discharge Criteria
- •Future Directions
- •Summary
- •References
- •8: General Postoperative Complications
- •Introduction
- •Risk Factors
- •Morbidities
- •Nutrition
- •Smoking
- •Preoperative Anemia
- •Sarcopenia
- •Obesity
- •Functional Exercise Capacity
- •Open Surgical Approach
- •Assessing Risk Factors
- •Addressing Risk Factors
- •Postoperative Complications
- •Gastrointestinal Complications (#1)
- •Ileus (Functional Bowel Obstruction)
- •Postoperative Small Bowel Obstruction (Mechanical Bowel Obstruction)
- •Hematologic Complications (#2)
- •Venous Thromboembolism
- •Infectious Complications (#3)
- •Surgical Site Infection (SSI)
- •Anastomotic Leaks
- •Wound Dehiscence
- •Other Infectious Complications
- •Pulmonary Complications (#4)
- •Postoperative Respiratory Failure
- •Pneumonia
- •Pulmonary Aspiration
- •Renal Complications (#5)
- •Acute Kidney Injury
- •Postoperative Urinary Retention
- •Cardiac Complications (#6)
- •Myocardial Infarction
- •Dysrhythmias
- •Neurological Complications (#7)
- •Perioperative Cerebrovascular Accidents
- •Sexual Dysfunction
- •Postoperative Delirium
- •Conclusion
- •References
- •9: Anastomotic Construction
- •Introduction
- •Operative Planning
- •Mobilization
- •Small Bowel Mobilization
- •Colonic Mobilization
- •Splenic Flexure Mobilization
- •Special Mobilization Techniques
- •Retroileal Anastomosis or Ileal Mesenteric Window
- •Right Colon De-Rotation (Deloyer’s Procedure)
- •Perfusion
- •Low Pelvic Anastomosis
- •Sutured Anastomosis
- •Stapled Anastomosis
- •Compression Ring Anastomosis
- •References
- •10: Anastomotic Complications
- •Anastomotic Leak
- •Risk Factors
- •Diagnosis
- •Outcomes After Anastomotic Leak
- •Anastomotic Fistula
- •Blind Loop Syndrome
- •Anastomotic Bleeding
- •Anastomotic Stricture
- •References
- •Anal Fissure
- •Medical/Pharmaceutical Treatment
- •Topical Agents
- •Botulinum Toxin Injection
- •Operative Treatment
- •Lateral Internal Sphincterotomy (LIS)
- •Technique
- •Outcomes
- •Local Advancement Flaps
- •Atypical Fissures
- •Anal Fissure, Conclusion
- •Anal Stenosis
- •Symptoms
- •Evaluation
- •Treatment
- •Nonoperative Treatment
- •Surgical Treatment
- •Rectal Advancement Flap
- •Y-V Advancement Flap
- •V-Y Advancement Flap
- •Diamond (Rhomboid) Flap
- •House Flap
- •U Flap (Island Flap Anoplasty)
- •Rotational S Flap
- •Technical Aspects
- •Flap Aftercare
- •Prevention
- •Anal Stenosis, Conclusions
- •References
- •Introduction
- •Cryptoglandular Pathophysiology
- •Cryptoglandular Abscess
- •Diagnosis
- •Treatment
- •Acute Fistula Management
- •Post-drainage Care
- •Post-drainage Antibiotics
- •Anal Fistula
- •Presentation/Symptoms
- •Fistulography
- •Computed Tomography (CT)
- •Magnetic Resonance Imaging (MRI)
- •Endoanal Ultrasound (EAUS)
- •Treatment Strategies
- •Fistulotomy
- •Setons
- •Draining Seton
- •Cutting Seton
- •Fibrin Glue
- •Fistula Plug
- •Endorectal Advancement Flap (ERAF)
- •Novel Surgical Therapies
- •Fistula Tract Laser Closure (FiLaC™)
- •Video-Assisted Anal Fistula Treatment (VAAFT)
- •Stem Cell Therapy
- •Recommendation
- •References
- •Introduction
- •Etiology
- •Clinical Presentation
- •Diagnostic Evaluation
- •Transanal Approach
- •Transperineal Approach
- •Posterior Approach
- •Transabdominal Approach
- •Other Approaches
- •Conclusion
- •References
- •15: Rectovaginal Fistula
- •Obstetrical
- •Crohn’s Disease
- •Cryptoglandular
- •Radiation Injury
- •Surgical Techniques
- •Perineal Approach
- •Episioproctotomy
- •Transverse Perineal Repair
- •Transrectal Approaches
- •Rectal Sleeve Advancement
- •Vaginal Approach
- •Tissue Transposition Repairs
- •Bioprosthetic Products
- •Abdominal Approaches
- •Conclusion
- •References
- •Pilonidal Disease
- •Introduction
- •Diagnosis
- •Treatment
- •Managing Patient Expectations
- •Nonsurgical Treatment
- •Antibiotics
- •Phenol
- •Fibrin Glue
- •Surgical Treatments
- •Complex Surgical Treatment
- •Karydakis Flap
- •Rhomboid Flap (aka Limberg Flap)
- •Cleft Lift Flap (Bascom Procedure)
- •Minimally Invasive Treatments
- •Trephination
- •Wound Healing Adjuncts
- •Hidradenitis Suppurativa
- •Introduction
- •Treatment
- •Medical Therapy
- •Topical Therapy
- •Systemic Antibiotics
- •Biologics
- •Other Medical Therapies
- •Laser Therapies
- •Surgery
- •Conclusions
- •References
- •Introduction
- •Pathophysiology
- •Etiology
- •Fecal Soilage
- •Dermatologic Diseases
- •Diagnostic Approach
- •Laboratory Testing
- •Treatment
- •First Encounter
- •Conclusions
- •References
- •Introduction
- •Anorectal Immunology
- •Asymptomatic
- •Symptomatic
- •Bacterial Sexually Transmitted Infections
- •Chlamydia
- •Diagnosis
- •Treatment
- •Lymphogranuloma Venereum
- •Diagnosis
- •Treatment
- •Gonorrhea
- •Diagnosis
- •Treatment
- •Syphilis
- •Diagnosis
- •Treatment
- •Chancroid
- •Diagnosis
- •Treatment
- •Donovanosis
- •Diagnosis
- •Treatment
- •Herpes Simplex Virus
- •Genital Warts
- •Giant Condyloma
- •Molluscum Contagiosum
- •Ectoparasitic Sexually Transmitted Diseases
- •Conclusion
- •References
- •19: Anal Intraepithelial Neoplasia
- •Introduction
- •Incidence
- •Epidemiology
- •Progression
- •Diagnosis
- •Treatment
- •Expectant Management
- •Topical Therapies
- •Trichloroacetic Acid (TCA)
- •5-Flurorouracil (5FU)
- •Cidofovir
- •Imiquimod
- •Local Ablative Therapies
- •Wide Local Excision
- •Treatment Summary
- •Surveillance/Prevention
- •Conclusion
- •References
- •20: Anal Cancer
- •Physical Examination
- •Radiologic Evaluation
- •Anal Anatomy
- •Perianal Squamous Cell Carcinoma
- •Anal Canal Squamous Cell Carcinoma
- •Chemotherapy
- •Radiation Therapy
- •Inguinal Lymph Node Metastases
- •Surgery
- •Surveillance
- •Anal Adenocarcinoma
- •Verrucous Carcinoma
- •Melanoma
- •Perianal Paget’s Disease (Intraepithelial Adenocarcinoma)
- •Basal Cell Carcinoma
- •Gastrointestinal Stromal Tumor (GIST)
- •Conclusion
- •References
- •21: Presacral Tumors
- •Introduction
- •Anatomic Considerations
- •Clinical Presentations
- •Physical Examination
- •Imaging Studies
- •Preoperative Biopsy
- •Tailgut Cysts
- •Enterogenous Cysts
- •Teratomas
- •Chordomas
- •Meningoceles
- •Neurogenic Tumors
- •Osseous Tumors
- •Miscellaneous Lesions
- •Currarino Syndrome
- •Management
- •Multidisciplinary Team
- •Neoadjuvant Therapy
- •Preoperative Considerations
- •Surgical Approach
- •Posterior Approach
- •Minimally Invasive Approaches
- •Outcomes
- •Conclusions
- •References
- •Introduction
- •Sporadic Versus Inherited Colorectal Cancer
- •Sporadic Colorectal Cancer
- •Mutations
- •Chromosomal Alterations
- •Right vs. Left CRC
- •Young Onset CRC
- •Epidemiology
- •Management
- •Inherited CRC
- •Lynch Syndrome (Hereditary Non-polyposis CRC)
- •Genetic Mutation
- •Lynch Syndrome Variants
- •Turcot Syndrome
- •Muir-Torre Syndrome
- •Familial CRC X
- •Screening Recommendations
- •Surgical Treatment
- •Medical Treatment
- •POLE/POLD1-Related Hereditary Cancer
- •Familial Adenomatous Polyposis
- •Genetic Mutations
- •Extracolonic Manifestations
- •Screening Recommendations
- •Attenuated FAP
- •Gardner Syndrome
- •Surgical Treatment
- •MUTYH-Associated Polyposis
- •Serrated Polyposis Syndrome
- •Diagnosis
- •Treatment
- •Hamartomatous Polyposis Syndromes
- •Juvenile Polyposis
- •Peutz-Jeghers Syndrome
- •Cowden Syndrome
- •Conclusion
- •References
- •Overview
- •Colorectal Cancer Precursor Lesions
- •Adenomas
- •Serrated Polyps
- •Colorectal Cancer Carcinogenic Pathways
- •Adenoma-Carcinoma Pathway
- •Serrated Pathway
- •Lesion Assessment
- •Endoscopic Mucosal Resection (EMR) Technique
- •Endoscopic Submucosal Dissection Technique
- •Recurrence Following Endoscopic Resection
- •Surveillance After Endoscopic Resection
- •Conclusion
- •References
- •Fecal Sampling
- •Flexible Sigmoidoscopy
- •Computed Tomography (CT) Colonography
- •Colonoscopy
- •Delineating Colon Versus Rectum
- •TNM Staging
- •History
- •Physical Examination
- •Proctoscopy
- •Colonoscopy
- •Tumor Localization
- •Blood Work
- •Imaging
- •Computed Tomography (CT) Scan
- •PET-CT
- •Endorectal Ultrasound
- •Preoperative Evaluation
- •Pathologic Features: Pre-Resection
- •Lymphovascular Invasion (LVI)
- •Perineural Invasion (PNI)
- •Tumor Budding
- •Tumor Grade
- •Histologic Type
- •Pathologic Factors: Post-Resection
- •Extranodal Tumor Deposits
- •Mesorectal Grade
- •Tumor Regression Score
- •Clinical or Imaging-Based Factors
- •Extramural Vascular Invasion (EMVI)
- •Circumferential Radial Margin (CRM) Status
- •Tumor Location
- •Conclusion
- •References
- •Introduction
- •Preoperative Tumor Localization
- •General Surgical Principles
- •No-Touch Technique
- •Lymphadenectomy
- •Mesocolic Excision
- •Adjacent Tissue or Organ Invasion
- •Technical Aspects
- •Hepatic Flexure Colon Cancer
- •Technical Aspects
- •Transverse Colon Cancer
- •Technical Aspects
- •Technical Aspects
- •Sigmoid Colon Cancer
- •Technical Aspects
- •Special Circumstances
- •References
- •26: Rectal Cancer: Neoadjuvant Therapy
- •Introduction
- •Rectal Cancer Staging
- •Adjuvant Radiation
- •Neoadjuvant Radiation
- •The Foundation Trials
- •Short- vs Long-Course Radiation
- •Total Neoadjuvant Chemoradiation Therapy (TNT)
- •Rationale
- •Systemic Chemotherapy Alone
- •Pathologic Complete Response
- •Consolidation vs Induction Chemotherapy
- •Conclusion
- •References
- •27: Rectal Cancer: Local Excision
- •Introduction
- •Patient Selection
- •T1N0
- •Predicting Lymph Node Metastasis
- •Tumor Budding
- •Techniques
- •Transanal Excision
- •Transanal Endoscopic Microsurgery
- •Transanal Minimally Invasive Surgery (TAMIS)
- •Complications
- •Oncologic Results
- •T1 Cancer
- •T2 Cancer
- •Salvage Surgery
- •Conclusion
- •References
- •28: Rectal Cancer: Nonoperative Management
- •Introduction
- •Rationale
- •Accidental Versus Intentional WW
- •Baseline Stage
- •Tumor Location
- •Endoscopic Features
- •Radiological Studies

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97. Nivatvongs S.Surgical management of malignant colorectal polyps. Surg Clin North Am. 2002;82:959–66.
98. Mohamed M, Schoeld JB. The pathology of colorectal polyps
and cancers (including biopsy). Surgery. 2014;32:165–71.

Colorectal Cancer: Preoperative
Evaluation andStaging
AmandaV.Hayman andCarol-AnnVasilevsky
24
Key Concepts
• The method chosen to screen a patient for colorectal cancer (CRC) should be individualized based on patient
comorbidities and life expectancy, access, cost, baseline
risk, compliance, and tolerance for invasive procedures
due to differing costs, sensitivities, and cadences of the
various options.
• Dening the anatomic location where the sigmoid colon
transitions to the rectum is increasingly determined by
cross-sectional imaging due to its reproducibility and is
less dependent on endoscopic localization alone, as body
habitus and gender can inuence the location of the peritoneal reection.
• Proper tumor localization and staging is essential to
establishing treatment recommendations; understanding
the pitfalls of each staging modality is important to avoid
under- or overtreatment.
• Magnetic resonance imaging (MRI) using a rectal cancer
protocol is now standard of care for locally advanced rectal tumors. Endorectal ultrasound (ERUS) is being used
less commonly as it is more operator dependent, less
reproducible, and invasive for the patient; however, ERUS
remains an important staging modality for early stage rectal tumors when determining eligibility for local
excision.
• A combination of histologic and radiographic factors
should be used to risk stratify CRC; higher-risk tumors
should be considered for more aggressive neoadjuvant
treatments; however, patient frailty or comorbidities
A. V. Hayman (*)
Division of Gastrointestinal & Minimally Invasive Surgery,
TheOregon Clinic, Portland, OR, USA
e-mail: ahayman@orclinic.com
C.-A. Vasilevsky
Department of Surgery, Jewish General Hospital,
Montreal, QC, Canada
may limit these treatment options and should be
individualized.
• Preoperative optimization and preparation of the colorectal cancer patient is essential to maximizing postoperative
and oncologic outcomes; a variety of tools, including
guidelines and checklists, are available to assist the surgical team in this endeavor.
Diagnosis ofColorectal Cancer
A diagnostic workup for colorectal cancer may follow a positive result from one of the various screening tests available
or follow investigation of symptoms, which may be acute or
subacute. A positive noninvasive screening test or unexplained iron-deciency anemia typically prompts colonoscopy, which then detects malignancy. Alternatively, a patient
may present with abdominal pain or distension and seek
emergent care. Cross-sectional imaging may then demonstrate an intraluminal lesion in the colon or rectum, resulting
in further workup.
Screening andDiagnostic Modalities
The ideal screening test for any disease should be easily
available, inexpensive, and noninvasive, with high sensitivity
and specicity. Because CRC is often asymptomatic, screening tests are universally recommended for patients starting at
either age 45 [1] or 50 [2] and ending between ages 75 and
86, based on the patient’s life expectancy and health status
(see Chap. 22). Once symptoms occur, the disease is typically in an advanced state with poorer survival rates.
There are a myriad of options for CRC screening; the
choice for a specic patient should be individualized based
on a constellation of factors, including personal and family
history of CRC or polyps, family history of inherited CRC
© Springer Nature Switzerland AG 2022
S. R. Steele etal. (eds.), The ASCRS Textbook of Colon and Rectal Surgery, https://doi.org/10.1007/978-3-030-66049-9_24
429

430
Table 24.1 Summary of the pros and cons of the most commonly used CRC screening modalities
Pros Cons
FOBT(fecal
occult blood
testing)
FIT Inexpensive
DNA-FIT Every 3years
Colonoscopy Can differentiate between polyps and cancer
Inexpensive
Noninvasive
Reduces CRC mortality by 15–33%
Convenient
Widely available
Noninvasive
No dietary/medication modication required
Higher specicity than FOBT (less chance of false positive for UGIB)
Comparable sensitivity to colonoscopy
Recommended by USPSTF
Covered by Medicare
92% sensitive for all CRC (less sensitive for stage IV)
Preventative (removes adenomas before they progress to cancer)
Diagnostic and therapeutic
Highest specicity/sensitivity
Longer time interval between tests (up to 10years)
Low specicity and sensitivity
Requires annual testing
Requires dietary/medication restrictions
Inaccurate in setting of benign GI bleeding (peptic
ulcers, hemorrhoids, diverticulosis)
Requires daily testing for 3days
Cannot differentiate between polyp and cancer
Positive test requires colonoscopy
Requires annual testing
Cannot differentiate between polyp and cancer
Positive test requires colonoscopy
Expensive, insurance may not cover
Minimal long-term data
Positive test requires colonoscopy
Higher false-positive rates
Less sensitivity for adenomas
Requires bowel preparation
Invasive with risk of serious complication
Typically requires sedation
Variable based on endoscopist skill
May not be widely available
Expensive
A. V. Hayman and C.-A. Vasilevsky
syndromes, personal history of inammatory bowel disease
(IBD), medical comorbidities, age/life expectancy, tolerance
for risk, anxiety, access to healthcare resources, compliance
with follow-up, and insurance coverage/cost.
It can be a confusing discussion for the physician to
choose the appropriate screening modality for his or her
patients. Understanding the benets and drawbacks is essential for the patient and physician to make the correct choice.
Table 24.1 may assist the healthcare team involved in this
decision-making. We cover the available diagnostic and
screening modalities for CRC below.
Fecal Sampling
The least invasive and most widely available screening test
for asymptomatic, average-risk persons is fecal sampling for
occult blood or tumor DNA.This method may be palatable
for some patients as it avoids mechanical bowel preparation
and is more practical in geographic areas with poor access to
endoscopy. These tests do not replace endoscopy, and it
should be noted that any positive test usually prompts colonoscopy. However, this initial triage test can conserve colonoscopy for a smaller population. The three fecal-based tests
available are discussed below:
• FOBT (fecal occult blood test): a guaiac-based test detects
presence of heme (nonprotein portion of hemoglobin) and
detects blood for all sources (including animal). Patients
are instructed to put a smear of their stool on a different
stool card 3 days in a row and then mail the cards in.
Testing is recommended on an annual basis. This is the
oldest stool-based test available and is quite inexpensive.
It requires dietary and medication modication for several days prior to the test, including avoiding red meat,
raw produce, antacids, vitamin C, nonsteroidal antiinammatory agents, loperamide, and iron supplements.
Menstruation is a relative contraindication. Relatively
low specicity and pretest dietary and medication restrictions have made it less attractive than newer stool tests [3]
• FIT (fecal immunochemical test): a.k.a. “safety- chemical”
method detects antibodies to the human protein globin
portion of hemoglobin found in red blood cells. This
results in less cross-reactivity to nonhuman blood and
improved specicity over FOBT [3]. It also requires only
a single card and thus better compliance. However, it is
still a test that is recommended to be performed
annually.
• Multitarget stool DNA-FIT (Cologuard®) test: combines
the FIT test with an additional test that detects genetic
mutations found in cancer cells ((KRAS, NDRG4, BMP3,
β-actin). It has a 13% false-positive and 8% false-negative
rate. It is recommended to be performed every 3years. It
was approved for use in 2014. However, it is relatively
expensive ($649 out-of-pocket) compared to other stool
assays and may not be covered by insurance. Further, it

24 Colorectal Cancer: Preoperative Evaluation andStaging
431
cannot differentiate between advanced polyps and adenocarcinoma [4, 5]
Flexible Sigmoidoscopy
Flexible sigmoidoscopy can examine the distal portion of the
colon and can be performed in an ofce setting with minimal
preparation and without sedation. Flexible sigmoidoscopy is
typically more easily tolerated than rigid proctoscopy and
can extend beyond 25cm. It has been suggested as a screening tool in younger adults since there is a higher incidence
ofleft-sided cancers in this population and was used historically in conjunction with barium enema. It is, however,
insufcient in older individuals due to a shift of polyps and
cancers to the more proximal colon. As such, it has been
combined with FIT or FOBT which theoretically enhances
detection.
Computed Tomography (CT) Colonography
CT colonography (CTC or “virtual colonoscopy”) is another
option available for screening. The technique involves
obtaining multiple thin-slice CTimages after carbon dioxide
insufation of the colon via a rectal tube, typically in two
positions (supine and lateral). The images are reconstructed
to give both two and three dimensional views of the colon
mucosa. The advantage of CTC is that it avoids the need for
sedation and may be preferable for patients with comorbidities who cannot undergo optical colonoscopy or who have a
tortuous colon. It does, however, require a full cathartic
bowel preparation prior to the procedure, and any suspicious
ndings usually prompt subsequent optical colonoscopy.
Patients are exposed to radiation and may have a risk of contrast nephropathy. It has comparable sensitivity to colonoscopy for polyps greater than 1cm but is less effective for
detecting smaller lesions as they are difcult to differentiate
from stool [4]. Since it involves the instillation of air or carbon dioxide into the rectum, it may be associated with
abdominal cramping and may rarely result in perforation. It
may also identify incidental abdominal ndings that may
require subsequent additional investigation. Lastly, this test
is typically not covered by Medicare. It can be difcult to
obtain insurance approval, despite receiving an “A” grade
from the US Preventive Services Task Force.
CTC is the procedure of choice in the setting of incomplete colonoscopy due to technical limitations, or an obstructing lesion, and provides better imaging resolution than more
traditional uoroscopic tests (i.e., contrast enema). However,
in the setting of a known malignancy, the costs and risks of
CTC should be considered in light of how treatment decisions would be altered by CTC ndings. If a patient has been
diagnosed with CRC and has an endoscopically obstructing
tumor of the proximal colon that does not allow for completion colonoscopy, it is unlikely that a CTC will provide any
ndings that would drastically change management, as the
colon proximal to the tumor will likely be resected. For
patients with endoscopically obstructing tumors of the distal
colon, CTC may be helpful to rule out synchronous tumors
preoperatively. However, it is also reasonable to forgo CTC,
as these patients will receive staging via CT scan which,
although not as sensitive as CT colonography, should at least
be able to detect any synchronous large lesions. Furthermore,
even if CTC does detect a small proximal lesion, it cannot be
biopsied in the setting of a distal untraversable lesion.
Therefore, in these settings, the patient’s clinical situation
needs to be carefully considered regarding the benet of any
further assessment for synchronous lesions. If the patient is
to undergo any neoadjuvant treatment, this will hopefully
allow completion colonoscopy after tumor shrinkage and
prior to surgical resection.
Colonoscopy
Colonoscopy is the most sensitive and specic test for
colorectal cancer and polyps, being both diagnostic (i.e.,
detects polyps and cancers), therapeutic (can remove polyps), and preventive (can prevent polyp progression to cancer). It can also detect other abnormalities, such as
inammatory bowel disease or diverticulosis. However, it is
the most invasive option, requiring full bowel preparation,
which is associated with nausea, vomiting, abdominal pain,
and dehydration, and is generally distasteful. It also carries
periprocedural risks, including colonic perforation (0.1%),
gastrointestinal bleeding (especially after biopsy or polypectomy), missing a lesion (false negative), or incomplete procedure (either knowingly or unknowingly, which occurs
about 5–10% of the time) [5]. Also, the quality of the procedure varies based on the performing physician’s technical
expertise, which can lead to false negatives. Lastly, most
rural areas have lower volume providers and less access to
endoscopy overall, often resulting in unacceptably long
travel times for patients.
If during colonoscopy a neoplasm is encountered, the
endoscopist should then consider the potential benets of
biopsy and tumor localization. For patients with obvious
adenomatous neoplasms of the intraperitoneal colon which
will clearly require colectomy, it could be argued that biopsy
results will be unlikely to change subsequent management
and may incur unnecessary cost to the patient, can exacerbate bleeding, carries a risk of perforation, and can have
false-negative results that only serve to confuse the patient.
However, biopsy may be helpful in detecting Lynch syndrome preoperatively (which may alter treatment decisions)

432
anal canal
Anal canal Anodem Anal verge
and help guide chemotherapeutic choices if the patient is
found to have incurable distant metastatic disease on preoperative staging and is to be treated nonoperatively. Moreover,
insurance companies may refuse to cover the cost of staging
tests without a histologic cancer diagnosis. If the etiology of
the lesion is in question, i.e., possible lymphoma or ischemic
ulcer, then biopsy is warranted. If the tumor is small and
unlikely to be appreciated from the serosal side intraoperatively, the distal extent of the tumor should be marked with
tattoo to assist with intraoperative localization (see Chaps.
23 and 25).
If a rectal tumor is encountered, biopsy should be performed routinely, and molecular testing including immunohistochemistry for mismatch repair proteins (IHC for MMR)
should be performed. Rectal cancer patients are often treated
with neoadjuvant radiotherapy and chemotherapy, which
may alter the tumor so that molecular analysis is not possible
postoperatively. In addition, some medical and radiation
oncologists will be reluctant to initiate neoadjuvant therapy
in a patient without histologic conrmation of adenocarcinoma. The distal extent of the tumor should be marked with
tattoo to ensure complete resection following neoadjuvant
therapy.
A. V. Hayman and C.-A. Vasilevsky
Delineating Colon Versus Rectum
Where the colon ends and the rectum begins is hotly debated.
The various potential modalities used to make this distinction include intraoperative visualization, endoscopy, and
cross-sectional imaging. A reproducible denition is important for numerous reasons, including eligibility for clinical
trials, localization for serial surveillance of rectal cancer,
determining treatment plans (i.e., upfront surgery versus
neoadjuvant chemoradiation), and for prognostic estimates.
The clinical implications are also critical, since rectal tumors
demonstrate clinical features that differ from colon tumors,
such as risk of peritoneal disease, lymphatic drainage, threatened radial and/or distal margins, consideration of sphincter
preservation, and need for protecting ileostomy.
According to the National Comprehensive Cancer
Network (NCCN) Clinical Practice Guidelines in Oncology,
the rectum is dened as beginning at a virtual line drawn
from the sacral promontory and symphysis pubis on magnetic resonance imaging (MRI) of the pelvis, ending at the
upper border of the anorectal ring [6, 7]. The rectum is arbitrarily divided into three parts, based on measurement on
rigid proctoscopy: low (0–6cm from the anal verge); mid
(7–11cm), and high (12–15cm) (Fig.24.1) [8].
Superior
rectal valve
Middle
rectal valve
Anorectal line
Pectinate
(dentate) line
Deep external
sphincter muscle
Internal
sphincter
muscle
Surgical
Anatomical
anal canal
Fig. 24.1 Delineation of the low, mid, and upper rectum with relevant landmarks
Inferior
rectal valve
Levator ani
muscle
Rectum
Anal
transition zone
Non-keratinized
squamous mucosa
Keratinized
squamous mucosa
8-9 cm
5-6 cm
4-5 cm
2.5-3 cm
0.5-1 cm

24 Colorectal Cancer: Preoperative Evaluation andStaging
433
Table 24.2 Commonly used criteria for delineating colon from
rectum
Intraoperative/
Surgical Criteria
- where the teniae
splay
- where the
epiploica
terminate at the
peritoneal
reection (varies
by gender)
the sacral
promontory
Cross-sectional imaging
(CT/MRI) Endoscopic
- a delineating line
between the sacral
promontory and the
pubic symphysis
- the sigmoid
“takeoff” from the
rectum (i.e., end of
the mesorectum),
seen as an acute
angulation
- distance from
the anal verge on
rigid
proctoscopy
(typically 12 or
15cm)
- beyond the third
rectal valve
Initial National Cancer Institute consensus guidelines [7]
used 12cm via rigid proctoscopy in the left lateral decubitus
position as the commonly accepted cutoff for the rectosigmoid junction. However, an international Delphi consensus
concluded that the “sigmoid takeoff” should be utilized, as
seen on cross-sectional imaging, marking a shift from a single clinician’s physical evaluation to a radiographic one [9].
One of the drivers behind this transition is the growing use of
MRI in staging newly diagnosed rectal cancers, buoyed by
the growth of programs such as the National Accreditation
Program for Rectal Cancer (NAPRC) [10], newer staging
guidelines, and criteria for clinical trial eligibility, all of
which favor, or even require, MRI for initial staging. The
purported benet of using MRI versus endoscopic evaluation
for staging is that imaging is more reproducible and thus
more easily interpreted and comparable over time in multidisciplinary discussions such as tumor boards. However,
there is still clear variation in all these denitions and a wide
variety of clinical implications for each modality, which will
be discussed later on in the chapter. In Table24.2, we compile the most commonly used criteria for delineating the
colon from the rectum.
Adding to this complexity is a newer algorithm for treating locally advanced colon cancer with upfront chemotherapy, as seen in the recently published FOxTROT trial [11].
This is also an option for bulky upper rectal cancers and is in
line with NCCN guidelines [7]. Although in daily practice it
can be challenging to denitiviely differentiate a colon from
a rectal location of the tumor, every attempt should be made
to do so as the clinical behavior and treatment recommendations differ.
Staging andWorkup ofColon andRectal
Cancer
Once the diagnosis of colorectal cancer has been established,
the extent of locoregional and distant spread should be determined. Many of the staging examinations are similar for
colon and rectal cancers. However, the locoregional staging
of rectal cancer does involve additional evaluation.
Appropriate staging is especially important for rectal cancer
as it drives treatment decisions in order to minimize underor overtreating the tumor, both of which have future implications with respect to prognosis and quality of life (see
Table24.3).
TNM Staging
Both colon and rectal cancers are staged according to the
American Joint Committee on Cancer (AJCC) TNM staging
system, eighth edition [12], which is based on the depth of
invasion of the tumor (T stage), the extent of lymph node
involvement (N stage), and the presence of distant metastases (M stage) (see Table 24.4). For rectal cancer, staging
requires consideration of both the initial clinical stage upon
which treatment decisions are made and the nal pathologic
stage which may be the most important prognosticator
(Table 24.5) [13]. The prex “c” for clinical is added to
denote an estimate of stage based typically upon radiographic imaging, and “p” is added to denote histologic staging postoperatively, while the prex “yp” is used to denote
histologic staging following neoadjuvant treatment [12].
History
Initial workup should include a complete tumor-specic history, such as duration of symptoms, abdominal or pelvic
pain, rectal bleeding and its characterization whether mixed
in with stool, bright red or maroon in color, tenesmus, incontinence, change in bowel habits (new onset constipation,
diarrhea, frequent thin stools), and weight loss. Patients may
also present with fatigue, shortness of breath, and reduced
endurance during exertion due to iron-deciency anemia.
Urinary problems, baseline fecal continence, and sexual
function should also be ascertained with regard to rectal cancers. In addition, family history should be elicited to rule out
the possibility of a hereditary or familial syndrome which
Table 24.3 Diagnostic workup of primary rectal cancer
Parameter Method of choice
Location (distance from anal
verge)
Visualization of colon Colonoscopy
Morphological verication Biopsy
cT stage
-Early ERUS, MRI
-Intermediate/advanced MRI, preferred over ERUS
-Sphincter inltration MRI, DRE, ERUS
cN stage MRIpreferred, CT, ERUS
M stage CT chest and abdomen, PET/CT if
Digital rectal exam (DRE)
Rigid sigmoidoscopy
Virtual colonography
extensive EMVI for other sites

434
Table 24.4 American Joint Committee on Cancer (AJCC) TNM Staging Classication for Colorectal Cancer 8th ed, 2017
T-PRIMARY TUMOR
Tx Primary tumor cannot be assessed
T0 No evidence of primary tumor
Tis Carcinoma in situ invasion of lamina propria
T1 Tumor invades submucosa
T2 Tumor invades muscularis propria
T3 Tumor invades subserosa or into non-peritonealized pericolic or perirectal tissue
T4 Tumor directly invades other organs or structure and/or perforates visceral peritoneum
T4a Tumor perforates visceral peritoneum
T4b Tumor directly invades other organs or structures
N -REGIONAL NODES
Nx Regional nodes cannot be assessed
N0 No regional lymph nodes identied
N1
N1a Metastasis in one regional node
N1b Metastasis in two to three regional lymph nodes
N1c No regional lymph nodes are positive, but there are tumor deposits, i.e., satellites in the subserosa or in
N2 Metastasis in four or more regional lymph nodes
N2a Metastasis in four to six regional lymph nodes
N2b Metastasis in seven or more regional lymph nodes
M -DISTANT METASTASIS
M0 No distant metastasis
M1 Distant metastasis
M1a Metastasis conned to one organ-liver, lung, ovary, non-regional lymph nodes without peritoneal metastasis
M1b Metastasis in more than one organ
M1c Metastasis to the peritoneum with or without other organ involvement
T categories
Although these categories have not changed, and T4 was divided into T4a and T4b in the previous edition, further clarication that tumors
with perforation in which tumor cells are continuous with the serosal surface through inammation are considered to be T4a. In the lower
rectum, in the absence of peritoneal covering, tumors that invade or directly adhere to adjacent organs or structures are considered T4b.
N categories
There is a discussion regarding isolated tumor cells in lymph nodes and micrometastases. Isolated cells consist of up to 20 cells within
subcapsular or marginal sinus of a lymph node should be designated N0 (or NOi+), but their presence does not change the state to stage
III.Micrometastases are clusters of 20 or more cells or metastases measuring >0.2mm and <2mm in diameter. Lymph nodes with
micrometastases are considered positive and designated N1. Outcomes in tumors with nodal micrometastases ranging from 0.2 to 2mm are
similar to those with metastases >2mm; thus the designation of N1mi is unnecessary.
The interpretation of discrete tumor nodules found within the lymph drainage area of the primary rectal carcinoma is claried. Nodules that
contain no identiable lymph tissue or vascular/neural structures should be considered tumor deposits and designated N1c. Tumor deposits
within a vessel wall should be considered lymphovascular invasion with the site-specic designations of L+ for lymphatic or small vein
invasion and V+ for deposits in endothelial cell-lined spaces with associated red blood cells or smooth muscle cells. If tumor nodules are
found around neural structures, they are classied as perineural invasion. N1c changes the disease to stage III even in the absence of nodal
metastases. The number of deposits has no inuence on the designation and is not added to the number of positive nodes.
M categories
M1c which denotes peritoneal metastases has been added
Key changes to AJCC staging of colorectal cancer [12]
Metastasis in one to three lymph nodes (tumor in lymph nodes measuring ≥0.2mm) or any number of
tumor deposits are present, and all identiable lymph nodes are negative
non-peritonealized pericolic or perirectal soft tissue without lymph node metastasis
A. V. Hayman and C.-A. Vasilevsky
would prompt genetic counseling and testing. Comorbidities
must be ascertained in order to establish suitability for surgical procedures or chemotherapy. The patient may warrant a
cardiology or pulmonary assessment, nutritional consult,
and, if appropriate, a geriatric evaluation including frailty
screening [14] prior to recommendation of treatment. Past
surgical history should also be queried since this may affect
choice of future surgical approach.
Physical Examination
On physical examination, the abdomen should be assessed
for previous scars, as well as palpable masses, hepatomegaly,
or abdominal distention, especially in the presence of
suspected obstruction. If the patient has a thin body habitus
and a large intra-abdominal luminal mass, it may be possible
to palpate the mass on abdominal exam. In the presence of a
high-grade obstruction, the patient may present with abdom-

24 Colorectal Cancer: Preoperative Evaluation andStaging
435
Table 24.5 American Joint Committee on Cancer (AJCC)
Stage 0 T1s N0 M0
Stage 1 T1,T2 N0 M0
Stage II T3, T4 N0 M0
Stage IIA T3 N0 M0
Stage IIB T4a N0 M0
Stage IIC T4b N0 M0
Stage III Any T N1,N2 M0
Stage IIIA T1, T2 N1 M0
T1 N2a M0
Stage IIIB T1, T2 N2b M0
T2, T3 N2a M0
T3, T4a N1 M0
T4a N2a M0
T4b N1, N2 M0
Stage IV Any T Any N M1
Stage IVA Any T Any N M1a
Stage IVB Any T Any N M1b
Stage IVC Any T Any N M1c
TNM Staging System for Colorectal Cancer 8th ed., 2017
inal distention and pain. For distal rectal tumors, perhaps the
most important diagnostic test is a thorough digital rectal
exam (DRE). If the lesion is palpable, the surgeon should
determine and document: percentage of luminal circumference involved; quadrant(s) involved; distance between the
distal margin of the tumor and the superior aspect of the anorectal ring; tactile characteristics (rm versus soft, mobile
versus tethered versus xed, etc.), and involvement of other
structures (anal sphincter muscles, posterior vaginal wall,
levator muscles, prostate). In addition, DRE allows the evaluation of sphincter bulk and tone, which is important should
restorative proctectomy be considered. DRE is limited in that
it can only be used to assess distal tumors that are within
range of the examining nger and may be also limited by
patient body habitus.
Proctoscopy
Proctoscopy should be performed by the operating surgeon
to determine the exact location of any tumor reported to be in
the rectosigmoid by the endoscopist at index colonoscopy,
prior to initiation of treatment. This examination is critical,
as determination of tumor location at index colonoscopy is
often inaccurate [15]. This is especially true for tumors
described as being in the “sigmoid” or “rectosigmoid” which
are subsequently found to be in the mid or distal rectum [15].
For rectal cancers, it is important to clearly delineate tumor
location relative to anatomic landmarks in order to determine
if sphincter-sparing surgery would be an option and to mark
the distal extent of the tumor with tattoo (see above). It is
also useful as a surveillance tool to assess tumor response to
neoadjuvant therapy. Proctoscopy can be performed in clinic
without sedation, with only an enema preparation in most
patients. Rigid proctoscopy requires less equipment, but one
cannot see beyond 25cm, and it can be challenging to see
lateral lesions. Furthermore, it can be quite uncomfortable
for some patients and technically difcult in patients with a
larger body habitus. Video exible proctosigmoidoscopy is
better tolerated by the patient and allows for photo documentation of tumor morphology and location; however, it is still
subject to the vagaries of exact delineation of distance as previously mentioned .
Colonoscopy
Colonoscopy is required to fully evaluate the colon after the
diagnosis of a colorectal malignancy or unresectable polyp
has been made to exclude synchronous cancers which may
occur in 3–5% of patients with primary rectal cancer as well
as synchronous polyps which occur in as many as 30% [16].
In general, sufcient biopsies of the tumor should be obtained
to conrm both the diagnosis of cancer, as well as to obtain
tissue for immunohistochemistry to ascertain biomarkers
which may guide chemotherapeutic options and prognosis.
Occasionally, there are conditions that may preclude a
complete examination of the colon preoperatively, such as
the presence of an obstructing lesion or perforation. In some
cases, a water-soluble contrast enema could be considered in
patients who present with acutely obstructing tumors of the
left colon or rectum, in order to rule out distal synchronous
large lesions and help prep the distal colon should intraoperative colonoscopy be required. CT with rectal contrast is
generally preferred over water-soluble enema due to threedimensional perspective, but typically the patient has already
received a CT in the emergency room, so the risks of a
repeated scan must be weighed against the benets.
Evaluation of the proximal colon may occasionally be
obtained via CT colonography in cases of partial obstruction
or deferred until the postoperative period or after reversal of
a diverting ileostomy. If a patient presents with a completely
obstructing colon or rectal cancer and either diverting loop
colostomy or Hartmann’s resection are performed, completion colonoscopy can be performed prior to resection or
Hartmann reversal via both limbs of the stoma or via the
colostomy and rectal stump to ensure that a synchronous
tumor or polyp will not be ignored at the time of reanastomosis. Another feasible option in the face of an obstructing
lesion is the placement of an endoscopic stent, which allows
the opportunity for biopsy and can serve as a bridge to surgery following resolution of the obstruction, as well as facilitate pre-treatment colonoscopy (See Chap. 25).
Tumor Localization
Endoscopic tattooing is recommended for all colonic lesions
for surgical localization. Endoscopic measurements either
via landmarks or centimeters from the anal verge are notoriously inaccurate. With the exception of the cecum, which has
distinct, reproducible anatomic landmarks (ileocecal valve,

436
A. V. Hayman and C.-A. Vasilevsky
appendiceal orice), the standard recommendation is submucosal tattooing with India ink distal to the tumor in at least
two quadrants.
However, because referring endoscopists may differ in
their routine practice, it is imperative that the surgeon communicate with the endoscopist regarding if and how a tumor
was marked with tattoo. This is especially important in the
setting of a malignant polyp that has been completely
removed endoscopically and is later found to have invasive
carcinoma, typically to the endoscopist’s surprise. In this
situation, the endoscopist should repeat the colonoscopy as
soon as possible in order to detect the polypectomy scar and
tattoo just distal to that site. This can be quite challenging in
the setting of multiple polypectomies and may require multiple tattoos, which poses treatment dilemmas for the operative surgeon [17, 18]. It is always favored to have the index
endoscopist perform the repeat colonoscopy for tattooing as
that individual will have the greatest chance of accurately
localizing the polypectomy site in question. These cases are
often best managed by a multidisciplinary discussion with
the surgeon and the endoscopist. Fortunately, even when the
polypectomy site may not be visible to the naked eye on
endoscopy, once the surgical resection specimen has been
xed, it can often be detected pathologically, conrming
resection of the appropriate segment.
As noted above, rectal tumors must be accurately localized prior to initiation of neoadjuvant treatment since
assessment of distal resection margins after treatment is
often difcult due to downstaging of the tumor. A few caveats should be mentioned. Tattooing with India ink for rectal
cancer has been found by some investigators to be inaccurate with error rates ranging from 2% to 21% [19]. It should
be remembered that submucosal tattoos that are placed preoperatively are often difcult to visualize from the abdomen because of the thick mesorectum. Some authors have
suggested that submucosal rectal wall tattoos be placed in
the operating room at the time of resection to accurately
mark the distal resection margin [20], although this may
not be possible in the setting of complete clinical response,
which is why placement of tattoo at the time of diagnosis is
favored. Unlike for intraperitoneal colon cancers, tattoo of
extraperitoneal rectal cancers will primarily be visible during intraoperative endoscopy, and a exible colonoscope/
sigmoidoscope or rigid proctoscope should be available for
localization during resection. Several case reports have also
raised the issue of potential tumor implantation by improper
endoscopic tattooing directly through the tumor, which
obviously should be avoided [21]. In addition, tattooing
may induce altered appearance of the rectal wall on MR or
reactive lymphadenopathy, with possible resultant overstaging on MRI [22]. Thus, if a rectal tumor was not tattooed at diagnosis, it is optimal to obtain staging MRI and
CT prior to marking the tumor endoscopically with ink. If
tattoo is placed transmurally, it can render resection more
difcult because the dye can obscure normal anatomic
planes [23]. As such, preoperative clipping has been suggested as a feasible alternative; however, clips carry the risk
of falling off [19].
Blood Work
Blood work including complete blood count, basic chemistry, and carcinoembryonic antigen (CEA) should be obtained.
CEA is used as a prognosticator whereby levels <5ng/ml
have been found to have better prognoses stage for stage as
opposed to CEA ≥5ng/ml [24]. Moreover, normalization of
previously elevated CEA levels in patients who were treated
with neoadjuvant treatment has been associated with complete pathologic response [25]. CEA levels that fail to normalize post-resection should raise the suspicion of metastatic
or residual disease. CEA should be routinely measured during surveillance of patients posttreatment since elevation of
previously normal levels may signal the development of
recurrent or metastatic disease. Routine testing for transaminases, bilirubin, and/or alkaline phosphatase, unless indicated for other reasons, is not necessary preoperatively as
they have been found to be neither sensitive nor specic for
the diagnosis of liver metastases and are no longer routinely
recommended by NCCN for staging or surveillance [6],
although their use is still advocated by the European Society
of Medical Oncology [26].
Imaging
Computed Tomography (CT) Scan
Initial staging includes CT scan of chest, abdomen, and pelvis in order to detect the presence of synchronous metastatic
disease which may be present in 30% of patients at presentation. CT scan of the chest is used to determine the presence
of lung metastases and to set a baseline for any preexisting
suspected benign lesions [7]. Its overall accuracy in detecting lung metastases is 84% with a sensitivity and specicity
of 73% and 74%, respectively [27]. CT will also detect indeterminate pulmonary lesions in 4–42% of patients; however,
upon further evaluation, only 1% are eventually conrmed as
metastases [28]. Abdominal CT will indicate the presence of
liver metastases, which may occur in 20–34% of patients [7].
CT is the most common imaging modality used to stage metastatic disease with an estimated sensitivity of 85%, positive
predictive value of 96%, and false-positive rate of 4% [29].
For liver lesions measuring <10mm, MRI outperforms CT
because of enhanced soft tissue resolution [30]. CT may also
demonstrate tumor-related complications such as perforation, obstruction, and invasion of adjacent organs and should
be done with both oral and IV contrast whenever possible. If
a patient has an iodine allergy, they can be prepped with steroids and diphenhydramine. In the case of renal insuf-
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