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IMAGING IN ULCERATIVE
COLITIS AND CHRONS DISEASE
PRESENTER  DR. VENKATESH
MODERATOR  DR. ANIL KUMAR
Introduction:
 Inflammatory bowel disease (IBD) is a fairly common enteropathy
that occurs in one per 1000 people in developed countries.
 The peak incidence of IBD is between the ages of 15 and 40 years,
with a possible second peak between 50 and 80 years.
 IBD is a heterogeneous group of chronic gastrointestinal disorders
with two broad subtypes: Crohn disease (CD) and ulcerative colitis
(UC).
 Ulcerative colitis is characterized by relapsing and remitting episodes
of inflammation limited to the colons mucosal layer. It almost
invariably involves the rectum, typically extends in a proximal, and
continues to involve other portions of the colon.
 Chrons disease can involve any component of the gastrointestinal
tract from the oral cavity to the anus and is characterized by trans-
mural inflammation. Extensive involvement of the right colon and
small intestine(Terminal ileum) is more common in CD.
Etiopathogenesis
 Highly complex and dependent on multiple factors.
 Occur in individuals who have aberrant genes which makes them
abnormally susceptible to commensal bacteria which are normally
present in the colon (intestinal microbiota) thus causing inflammation
in the colonic mucosa. These interactions between the mucosa of the
colon and colon commensals are triggered by exposure to risk factors
in the environment.
imaging in uc and chrons disease (1).pptx
Risk and Protective Factors for UC and CD
Ulcerative Colitis Crohns Disease
RISK FACTORS: RISK FACTORS:
Higher socioeconomic status (hygiene hypothesis),
Previous h/o enterocolitis,
NSAIDs use,
OC pills
Higher socioeconomic status (hygiene hypothesis)
NSAIDs use,
OC pills, Antibiotic use in childhood,
Smoking
PROTECTIVE FACTORS: PROTECTIVE FACTORS:
Breastfeeding,
Smoking,
Appendicectomy
Breast feeding
Clinical presentation
 Diarrhea and rectal bleeding > 6 weeks (UC > CD).
 Tenesmus (Rectal inflammation).
 The severity of patient presenting with colitis can be graded as mild,
moderate and severe based on the clinical presentation and physical
signs.
 Inflammatory markers :
serum  ESR
stool - Fecal cal protein.
Diagnostic algorithm for confirmation of IBD
diagnosis
IMAGING MODALITIES
 Two groups of imaging modalities are available for the evaluation of IBD.
Imaging modalities that allow assessment of the bowel lumen, bowel wall, and
the extraintestinal abdomen, represented by the cross-sectional imaging
modalities: ultrasonography (US), CT enterography, and magnetic resonance (MR)
enterography.
Imaging modalities that evaluate exclusively the bowel lumen: small-bowel follow-
through (SBFT) and barium enema examinations.
SBFT and Barium Enema Examinations
ADVANTAGES
 Dynamic evaluation of the whole gastrointestinal tract
 Allows manual mobilization of the bowel
DISADVANTAGES
 Ionizing radiation
 Limited in the evaluation of the intestinal wall
 It does not allow panoramic view of the abdominal cavity.
ADVANTAGES
 Low cost
 Can be repeated as many times as necessary
 Absence of ionizing radiation or contrast medium
DISADVANTAGES
 Operator dependent
 Limited because of intestinal gas distribution
 It does not allow panoramic view of the abdominal cavity.
US Examination
CT ENTEROGRAPHY
MR ENTEROGRAPHY
ADVANTAGES
- Thin section
- Widely available
- The optimal method for depicting extraluminal bowel gas and complex
abdominal fistulas
DISADVANTAGES
- Ionizing radiation
- Lower contrast resolution of the bowel wall
- Intravenous iodinated contrast material necessary
ADVANTAGES
- High contrast resolution
- Allows functional evaluations
- Can be performed without the use of intravenous contrast material
- The optimal method to evaluate perianal fistulas
DISADVANTAGES
- Higher cost and less availability
- Contraindications related to the magnetic field and paramagnetic contrast
material
Systemic approach
 I - Inflammatory mesentery
 B - Bowel wall changes
 D - Disease complications
B
I D
1. LYMPHADENOPATHY
2. FAT CHANGES
3. ENGORGED
VESSELS
LUMINAL
1. STRICTURES
2. DILATATIONS
3. CANCER
EXTRALUMINAL
4. FISTULA
5. ABSCESS
6. PERFORATION
1. THICKENING
2. STRATIFICATION
3. PERMANENT
STRUCTURAL
CHANGES
imaging in uc and chrons disease (1).pptx
INFLAMMATORY
MESENTERY
GROU
P 1
FAT STRANDING:
 The sharp interface between bowel and mesentery is lost due to
influx of inflammatory cells and fluid.
 The enhancement of perienteric fat is used as a severity marker of
IBD in imaging-based indices (MR imaging and Sailer index), and
recent studies have shown that diffusion-weighted imaging is
equivalent for the detection of small-bowel inflammation.
 Fat stranding: active inflammation marker .
FAT STRANDING:
FIBROFATTY PROLIFERATION
 Fibrofatty proliferation, also called creeping fat or fat wrapping,
represents the asymmetric proliferation of fat usually along the
mesenteric border, which is almost exclusively seen in CD.
 This mesenteric adipose tissue hypertrophy causes an asymmetric
displacement of mesenteric vessels and isolation of the bowel from
the surrounding bowel loops.
 Fibrofatty proliferation: inactive and chronic inflammation marker.
FIBROFATTY PROLIFERATION
ENGORGED VASA RECTA
 Engorged vasa recta represents vascular dilatation on the mesenteric
side of the bowel.
 This is also known as the comb sign because the engorged vessels
have a linear appearance, resembling the teeth of a hair comb.
 Engorged vasa recta: active inflammation marker
ENGORGED VASA RECTA
LYMPHADENOPATHY:
 Reactive mesenteric lymphadenopathy is characterized by hyperenhancing
lymph nodes that typically range from 3 to 8 mm.
 Lymphadenopatathy is commonly found in patients with IBD, both CD and UC,
although it is more commonly seen with CD.
 The lymph nodes may be detected more frequently at the mesenteric root,
the mesenteric periphery, or in the right lower abdominal quadrant.
 When lymph nodes are multiple and larger than 10 mm, the possibility of
tumor should be considered, mainly lymphoma and carcinoma.
 Mesenteric lymphadenopathy: active inflammation marker
imaging in uc and chrons disease (1).pptx
BOWEL WALL
GRO
UP 2
HOMOGENEOUS THICKENING:
 Bowel wall thickening is defined as a small bowel wall thickness greater
than 3 mm in a distended loop.
 In homogeneous bowel thickening, the parietal bowel wall is enlarged
without mural stratification.
 It can be asymmetric with increased thickening on the mesenteric side
of the bowel, mainly in CD.
 Homogeneous thickening without enhancement may represent active
or inactive inflammation marker.
 Homogeneous thickening with enhancement: active inflammation
marker
BILAMINAR STRATIFICATION:
 Bowel wall thickening with bilaminar stratification results from the
association of mucosal hyperenhancement and submucosal
edema.
 Submucosal edema is a severity marker used in imaging-based IBD
indexes. It is not specific for IBD and may be seen in other small
bowel inflammatory conditions, such as ischemia and radiation
enteritis.
 Bilaminar stratification: active inflammation marker
imaging in uc and chrons disease (1).pptx
TRILAMINAR TRILAMINAR:
FAT HALO SIGN:
 The fat halo sign represents infiltration of the submucosa with fat
between the muscularis propria and the mucosa.
 It may be indicative of IBD, although it has been reported in
cytoreductive therapy and graft-versus-host disease.
 In the absence of clinical or radiologic evidence of IBD, the presence
of the fat halo sign may represent a normal finding.
 Inactive inflammation marker.
imaging in uc and chrons disease (1).pptx
PERMANENT STRUCTURAL CHANGES:
GROU
P 3 DISEASE COMPLICATIONS
COLORECTAL CANCER
 Colorectal cancer has a
higher incidence in patients
with long-standing IBD.
 The risk is related to the
duration and anatomic
extent of the disease.
PITFALL: inflammatory or malignant?
When we need to think of malignant wall thickening
 When thickening of bowel wall can
be described as
 Focal (<5 cm)
 Irregular or asymmetric
 Heterogeneous
 Perienteric fat stranding
disproportionally less severe than
the degree of wall thickening
When thickening of bowel wall can be
described as
 Segmental or diffuse (640 cm or >40 cm)
 Regular, circumferential, symmetric
 Homogeneous
 Perienteric fat stranding disproportionally
more severe than the degree of wall
thickening
NEOPLASTIC CONDITION INFLAMMATORY CONDITION
imaging in uc and chrons disease (1).pptx
STRICTURES AND DILATATIONS
TOXIC MEGACOLON
 Toxic megacolon is a potentially lethal complication of IBD that is characterized
by total or segmental nonobstructive colonic dilatation associated with systemic
toxicity. It can occur in colitis caused by UC and CD.
 The diagnosis is made by a combination of symptoms and clinical signs:
 Radiographic evidence of colonic dilatation
 Any three of the following: fever (>101.5 属F), tachycardia (>120 beats per
minute), leukocytosis (>10.5 x 103
/袖L), or anemia
 Any one of the following: dehydration, altered mental status, electrolyte
abnormality, or hypotension
 Imaging findings include: bowel wall thickening, loss of haustra, and segmental
or total colonic dilatation of at least 5 cm (CT) and 8 cm (supine radiograph
imaging in uc and chrons disease (1).pptx
PERFORATION
FISTULA
 Fistula is a permanent abnormal passageway between
two organs. The clinical course is variable and
depends on the location and complexity.
 Fistulas may be external (arise from the intestine and
communicate with the skin) or internal (enteroenteric
or between the bowel and adjacent organs). The most
common fistulas are enterocutaneous and perianal.
 When compared with surgical findings, CT
enterography has a reported accuracy of 86% for
fistulas, with a false-negative rate of 8%.
ABSCESS
PERIANAL ABSCESS:
 Dilatation of the vasa recta
 Fibrofatty proliferation
Mural stratification
 Colonic wall thickening
 Mural thickening: 1113 mm, eccentric and discontinuous
 Skip lesions (pathognomonic)
 Right colon and terminal ileum
CHRONS DISEASE ULCERATIVE COLITIS
INFLAMMATORY MESENTERY
BOWEL WALL CHANGES
 Dilatation of the vasa recta
DISEASE COMPLICATIONS
 Postinflammatory polyps
 Fistulas, abscesses
 Mural stratification
 Colonic wall thickening
 Mural thickening: 8 mm, symmetric and continuous
 Postinflammatory polyps
 Toxic megacolon
DIFFERENTIAL DIAGNOSIS:
TUBERCULOSIS ISCHEMIC COLITIS
imaging in uc and chrons disease (1).pptx
ANGIOEDEMA OF THE SMALL BOWEL
PSEUDOMEMBRANOUS COLITIS
TYPHLITIS INFECTIOUS ENTEROCOLITIS
THANK YOU

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imaging in uc and chrons disease (1).pptx

  • 1. IMAGING IN ULCERATIVE COLITIS AND CHRONS DISEASE PRESENTER DR. VENKATESH MODERATOR DR. ANIL KUMAR
  • 2. Introduction: Inflammatory bowel disease (IBD) is a fairly common enteropathy that occurs in one per 1000 people in developed countries. The peak incidence of IBD is between the ages of 15 and 40 years, with a possible second peak between 50 and 80 years. IBD is a heterogeneous group of chronic gastrointestinal disorders with two broad subtypes: Crohn disease (CD) and ulcerative colitis (UC).
  • 3. Ulcerative colitis is characterized by relapsing and remitting episodes of inflammation limited to the colons mucosal layer. It almost invariably involves the rectum, typically extends in a proximal, and continues to involve other portions of the colon. Chrons disease can involve any component of the gastrointestinal tract from the oral cavity to the anus and is characterized by trans- mural inflammation. Extensive involvement of the right colon and small intestine(Terminal ileum) is more common in CD.
  • 4. Etiopathogenesis Highly complex and dependent on multiple factors. Occur in individuals who have aberrant genes which makes them abnormally susceptible to commensal bacteria which are normally present in the colon (intestinal microbiota) thus causing inflammation in the colonic mucosa. These interactions between the mucosa of the colon and colon commensals are triggered by exposure to risk factors in the environment.
  • 6. Risk and Protective Factors for UC and CD Ulcerative Colitis Crohns Disease RISK FACTORS: RISK FACTORS: Higher socioeconomic status (hygiene hypothesis), Previous h/o enterocolitis, NSAIDs use, OC pills Higher socioeconomic status (hygiene hypothesis) NSAIDs use, OC pills, Antibiotic use in childhood, Smoking PROTECTIVE FACTORS: PROTECTIVE FACTORS: Breastfeeding, Smoking, Appendicectomy Breast feeding
  • 7. Clinical presentation Diarrhea and rectal bleeding > 6 weeks (UC > CD). Tenesmus (Rectal inflammation). The severity of patient presenting with colitis can be graded as mild, moderate and severe based on the clinical presentation and physical signs.
  • 8. Inflammatory markers : serum ESR stool - Fecal cal protein.
  • 9. Diagnostic algorithm for confirmation of IBD diagnosis
  • 11. Two groups of imaging modalities are available for the evaluation of IBD. Imaging modalities that allow assessment of the bowel lumen, bowel wall, and the extraintestinal abdomen, represented by the cross-sectional imaging modalities: ultrasonography (US), CT enterography, and magnetic resonance (MR) enterography. Imaging modalities that evaluate exclusively the bowel lumen: small-bowel follow- through (SBFT) and barium enema examinations.
  • 12. SBFT and Barium Enema Examinations ADVANTAGES Dynamic evaluation of the whole gastrointestinal tract Allows manual mobilization of the bowel DISADVANTAGES Ionizing radiation Limited in the evaluation of the intestinal wall It does not allow panoramic view of the abdominal cavity. ADVANTAGES Low cost Can be repeated as many times as necessary Absence of ionizing radiation or contrast medium DISADVANTAGES Operator dependent Limited because of intestinal gas distribution It does not allow panoramic view of the abdominal cavity. US Examination
  • 13. CT ENTEROGRAPHY MR ENTEROGRAPHY ADVANTAGES - Thin section - Widely available - The optimal method for depicting extraluminal bowel gas and complex abdominal fistulas DISADVANTAGES - Ionizing radiation - Lower contrast resolution of the bowel wall - Intravenous iodinated contrast material necessary ADVANTAGES - High contrast resolution - Allows functional evaluations - Can be performed without the use of intravenous contrast material - The optimal method to evaluate perianal fistulas DISADVANTAGES - Higher cost and less availability - Contraindications related to the magnetic field and paramagnetic contrast material
  • 14. Systemic approach I - Inflammatory mesentery B - Bowel wall changes D - Disease complications
  • 15. B I D 1. LYMPHADENOPATHY 2. FAT CHANGES 3. ENGORGED VESSELS LUMINAL 1. STRICTURES 2. DILATATIONS 3. CANCER EXTRALUMINAL 4. FISTULA 5. ABSCESS 6. PERFORATION 1. THICKENING 2. STRATIFICATION 3. PERMANENT STRUCTURAL CHANGES
  • 18. FAT STRANDING: The sharp interface between bowel and mesentery is lost due to influx of inflammatory cells and fluid. The enhancement of perienteric fat is used as a severity marker of IBD in imaging-based indices (MR imaging and Sailer index), and recent studies have shown that diffusion-weighted imaging is equivalent for the detection of small-bowel inflammation. Fat stranding: active inflammation marker .
  • 20. FIBROFATTY PROLIFERATION Fibrofatty proliferation, also called creeping fat or fat wrapping, represents the asymmetric proliferation of fat usually along the mesenteric border, which is almost exclusively seen in CD. This mesenteric adipose tissue hypertrophy causes an asymmetric displacement of mesenteric vessels and isolation of the bowel from the surrounding bowel loops. Fibrofatty proliferation: inactive and chronic inflammation marker.
  • 22. ENGORGED VASA RECTA Engorged vasa recta represents vascular dilatation on the mesenteric side of the bowel. This is also known as the comb sign because the engorged vessels have a linear appearance, resembling the teeth of a hair comb. Engorged vasa recta: active inflammation marker
  • 24. LYMPHADENOPATHY: Reactive mesenteric lymphadenopathy is characterized by hyperenhancing lymph nodes that typically range from 3 to 8 mm. Lymphadenopatathy is commonly found in patients with IBD, both CD and UC, although it is more commonly seen with CD. The lymph nodes may be detected more frequently at the mesenteric root, the mesenteric periphery, or in the right lower abdominal quadrant. When lymph nodes are multiple and larger than 10 mm, the possibility of tumor should be considered, mainly lymphoma and carcinoma. Mesenteric lymphadenopathy: active inflammation marker
  • 27. HOMOGENEOUS THICKENING: Bowel wall thickening is defined as a small bowel wall thickness greater than 3 mm in a distended loop. In homogeneous bowel thickening, the parietal bowel wall is enlarged without mural stratification. It can be asymmetric with increased thickening on the mesenteric side of the bowel, mainly in CD. Homogeneous thickening without enhancement may represent active or inactive inflammation marker. Homogeneous thickening with enhancement: active inflammation marker
  • 28. BILAMINAR STRATIFICATION: Bowel wall thickening with bilaminar stratification results from the association of mucosal hyperenhancement and submucosal edema. Submucosal edema is a severity marker used in imaging-based IBD indexes. It is not specific for IBD and may be seen in other small bowel inflammatory conditions, such as ischemia and radiation enteritis. Bilaminar stratification: active inflammation marker
  • 31. FAT HALO SIGN: The fat halo sign represents infiltration of the submucosa with fat between the muscularis propria and the mucosa. It may be indicative of IBD, although it has been reported in cytoreductive therapy and graft-versus-host disease. In the absence of clinical or radiologic evidence of IBD, the presence of the fat halo sign may represent a normal finding. Inactive inflammation marker.
  • 34. GROU P 3 DISEASE COMPLICATIONS
  • 35. COLORECTAL CANCER Colorectal cancer has a higher incidence in patients with long-standing IBD. The risk is related to the duration and anatomic extent of the disease.
  • 36. PITFALL: inflammatory or malignant? When we need to think of malignant wall thickening When thickening of bowel wall can be described as Focal (<5 cm) Irregular or asymmetric Heterogeneous Perienteric fat stranding disproportionally less severe than the degree of wall thickening When thickening of bowel wall can be described as Segmental or diffuse (640 cm or >40 cm) Regular, circumferential, symmetric Homogeneous Perienteric fat stranding disproportionally more severe than the degree of wall thickening NEOPLASTIC CONDITION INFLAMMATORY CONDITION
  • 39. TOXIC MEGACOLON Toxic megacolon is a potentially lethal complication of IBD that is characterized by total or segmental nonobstructive colonic dilatation associated with systemic toxicity. It can occur in colitis caused by UC and CD. The diagnosis is made by a combination of symptoms and clinical signs: Radiographic evidence of colonic dilatation Any three of the following: fever (>101.5 属F), tachycardia (>120 beats per minute), leukocytosis (>10.5 x 103 /袖L), or anemia Any one of the following: dehydration, altered mental status, electrolyte abnormality, or hypotension Imaging findings include: bowel wall thickening, loss of haustra, and segmental or total colonic dilatation of at least 5 cm (CT) and 8 cm (supine radiograph
  • 42. FISTULA Fistula is a permanent abnormal passageway between two organs. The clinical course is variable and depends on the location and complexity. Fistulas may be external (arise from the intestine and communicate with the skin) or internal (enteroenteric or between the bowel and adjacent organs). The most common fistulas are enterocutaneous and perianal. When compared with surgical findings, CT enterography has a reported accuracy of 86% for fistulas, with a false-negative rate of 8%.
  • 45. Dilatation of the vasa recta Fibrofatty proliferation Mural stratification Colonic wall thickening Mural thickening: 1113 mm, eccentric and discontinuous Skip lesions (pathognomonic) Right colon and terminal ileum CHRONS DISEASE ULCERATIVE COLITIS INFLAMMATORY MESENTERY BOWEL WALL CHANGES Dilatation of the vasa recta DISEASE COMPLICATIONS Postinflammatory polyps Fistulas, abscesses Mural stratification Colonic wall thickening Mural thickening: 8 mm, symmetric and continuous Postinflammatory polyps Toxic megacolon
  • 48. ANGIOEDEMA OF THE SMALL BOWEL PSEUDOMEMBRANOUS COLITIS