GI Flashcards

1
Q
A

Candidiasis

irregular, longitudinal plaques with intervening normal mucosa

Typically upper 1/3 oesophagus

Immunocompromised (HIV, Transplant)

In older asymptomatic patients = Mucosal white plaques more uniform, rounded, and less well defined than candidiasis = Glycogenic Acanthosis

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2
Q
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Herpes ulcer

Immunocompromised, multiple small <1cm oesophageal ulcers with a surrounding halo of oedema

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3
Q
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CMV or HIV

Singular large flat ulcer. 1cm in length in the oesophagus

HIV more common to have massive ulcer (can be several cms)

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4
Q
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Barretts

Mid oesophageal stricture, associated hiatal hernia and reflux

‘reticular muscosal pattern’

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5
Q
A

Eosinophilic oesophagitis

Barium - Concentric, ring-like strictures of oesophagus

**Not transient - Permanent **

DDx
feline oesophagus
- folds1-2 mm thick and run horizontally around the entire circumference of the esophageal lumen.
- The findings are transient, seen following reflux and not during swallowing.
- Associated with GORD
- distal two-thirds of the thoracic esophagus

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6
Q
A

Caustic

long stricture ± diffuse ulceration of lower and mid oesophagus

Stomach can be pulled into the chest as the oesophagus shortens and strictures

DDX Long stricture
-NG tube in too long or radiation - These are usually smooth

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7
Q
A

oesophageal scleroderma

-affects the Lower 2/3 (smooth muscle) with atony and peristalsis that begin caudally and moves cranially.
-Moderate dilatation of esophagus with fusiform stricture at lower end

Nb upper 1/3 to above aortic arch is normal (striated muscle)

NB - Jejunum - dilated but with preserved valvulae conniventes

DDx
Achalsia
- Grossly dilated whole oesophagus with smooth, beak-like tapering at lower end

Reflux Esophagitis (With Stricture)
-Longer tapered distal stricture
-Less luminal dilation
-Distinguished from scleroderma by normal peristalsis

Esophageal Carcinoma
-Abrupt proximal borders of strictured segment (rat tail appearance)
-Mucosal irregularity, shouldering, mass effect

Nb polymositits
- affects skeletal muscle so therefore affects the upper third of oesophagus, retention of barium in the valeeculae, regurg nasal reflux, failure of contrast to progress in upper third without gravity

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8
Q
A

Oesophageal duplication cyst

Water density cyst in the posterior mediastinum

Commonest site-** distal ileum**, duodenum, oesophagus

DDx
- Bronchogenic cyst - Cartilage, **subcarinal **
- Leiomyoma - solid oesophageal mass
- Oesophageal diverticulum - communicated directly
- Neurenteric cyst - associated vertebral abnormalities

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9
Q
A

Zenker Diverticulum

Outpouching with rounded contour posteriorly in the neck is above the cricopharyngeus muscle

In hypopharynx!!!

Site of weakness is the Killian dehiscence - between the inferior pharyngeal constrictor muscle and cricopharyngeal muscle

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10
Q
A

Traction diverticulum

Dysphagia in elderly person. Previous TB.
Barium-filled tented or triangular outpouching in the mid oesophagus

Acquired condition due to subcarinal or perihilar granulomatous lymph node pathology (TB, histo)

External force on oesophageal wall, such as mediastinal inflammation, that adheres and pulls on oesophageal wall

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11
Q
A

Killian - Jamieson Diverticulum

Small outpouching in the cervical oesophagus. Anterior and lateral direction

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12
Q
A

Epiphrenic diverticulum

Large saccular outpouching just above the diaphragm, right side

Can be mistaken for paraesophageal hernia - usually in on the left

associated with dysmotility disorders

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13
Q
A

Oesophageal pseudodiverticulosis

Barium - multiple, tiny (1- to 4-mm depth), flask-like outpouchings in the oesophagus

Barium trapped in dilated excretory ducts of submucosal glands

CHRONIC REFLUX* and Candida

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14
Q
A

Plummer - Vinson syndrome

Oesophageal web, iron deficiency anaemia, dysphagia, spoon shaped nails

Webs are risk factor for hypopharyngeal and oesophageal Cancer

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15
Q
A

Pulmonary sling

Aberrant left pulmonary artery

Anterior indentation of the oesophagus and posterior indentation of the trachea

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16
Q
A

GIST

Well-circumscribed.
**Heterogenous, central necrosis is key **

Hypervascular

submucosal mass extending exophytically from GI tract
Stomach (60%) , dudoenum (30%) and oesophagus (10%)

Remember
- assocaited NF-1
- Carneys triad
- Pulmonary condromas, Exrtra-adrenal paragangliomas, GIST

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17
Q
A

Gastric lymphoma

Diffuse wall thickening
can cross the pylorus
Rarely causes gastric outlet obstruction

can be primary MALT and secondary to systemic lymphoma (NHL)

DDX
Hematogenous spread of metastases to stomach

Malignant melanoma
Bull’s-eye or target lesions, nodular intramural cavitated lesions

Breast cancer: Linitis plastica or leather bottle appearance
Markedly thickened gastric wall with enhancement, folds preserved
Mimics primary scirrhous carcinoma of stomach

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18
Q
A

gastric carcinoma

  1. Intraluminal mass with no peristalsis through lesion (at fluoroscopy)
    - Antral mass causing outlet obstruction
  2. Ulcer -
    Width > depth, nodular edges
    obliteration of surrounding areae gastricae
  3. Infiltrative -
    Diffuse infiltration of gastric wall; non-peristaltic, non-distensible = **Linitis plastica (leather bottle) ***
    **Pseudoachalasia: Fundal carcinoma may destroy myenteric plexus
    Oesophageal obstruction, dilated lumen, diminished peristalsis; mistaken for primary achalasia - Pseudo the GE junction doesnt relax

Krukenberg tumor: Metastases to ovaries via peritoneal seeding
Early epigastric nodes

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19
Q
A

Menetriers disease

SPARES the antrum

Hyperplastic gastropathy/ protein-losing gastropathy

Grossly thickened, lobulated folds in gastric fundus and body with poor barium coating. low albumin

CT - Massive thickening of mucosa and submucosa, giant, mass-like, tortuous folds resemble cerebral convolutions

DDx
Gastritis - thickened lobulated folds favour antrum
ZES - Multiple ulcers, pancreatic tumor (gastrinoma)

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20
Q

Types of gastric volvulus?

A
  1. Organoaxial
    - Greater curvature flips over the lesser.
    - Older people
    - Associated with paraesophageal hernia
  2. Mesenteroaxial
    - Twisting over the mesentery
    - ischaemia, obstruction
    - kids
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21
Q
A

Whipples disease

Nodular thickening of jejunal folds

+ LOW density (near fat) mesenteric lymphadenopathy

Pseduo whipples
MAI infection in AIDS patient CD$ <100
Nodules in jejenum
+ Splenomegaly and retroperitoneal lymph nodes

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22
Q
A

small bowel adenocarcnioma

Proximal small bowel usually, Jejunum . present with SBO!!

**Increased incidence with coeliac disease
**
Focal circumferential bowel wall thickening in the proximal small bowel

DDx
Small bowel lymphoma
- immunosuppression - transplant, AIDS
- usually **do not obstruct, lumen can be aneurysmal and not narrow
**
Carcicnoid
- distal small bowel - terminal ileum and appendix

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23
Q
A

Carcinoid

spiculated mesenteric mass with calcification/ desmoplastic reaction

Tethering of SB loops

90% arise in terminal ileum/appendix

Hyper-vascular liver mets - Carcinoid syndrome

111I- Octreotide scans (1st - highest sensitivity)
or 123I-MIBG (for 10% dont take up octreotide)
for Dx and staging

Big centres use gallium PET

Assocaited with MEN 1 or MEN 2a

DDX

Sclerosing mesenteritis/ mesenteric pannicultuis
- FAT HALO sign - Mass envelop vessels, but preservation of fat around vessels
- usually jejunal small bowel mesentery

Gastrointestinal Stromal Tumor (GIST)
- Hypervascular tumor, not associated with desmoplastic effect on mesentery

Small Bowel Carcinoma
- More common in duodenum or jejunum than in ileum
- Causes luminal obstruction
- Mass and metastases are hypovascular

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24
Q
A

Desmoid tumour

Small bowel mesentery or abdominal wall mass arising at site of scarring from prior surgery

Associated with Gardner syndrome or familial adenomatous polyposis (FAP), usually intraabdominal

Soft tissue mass with well-defined or ill-defined margins

variable, heterogeneous enhancement on CECT

can infiltrate into bowel wall/adjacent structures, can cause SBO

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25
Q

Key difference between direct and indirect hernia?

A

Direct
- Medial to inferior epigastric artery
- Defect in Hesselbacks triangle

Indirect
- most common
- lateral to the inferior epigastric artery
- Covered by internal spermatic fascia
- failure of Processus vaginalis to close

26
Q

Features of femoral hernia?

A

Old females
Medial to femoral vein
Posterior to the inguinal ligament
Usually on the right

27
Q

DDx for stenois of terminal ileum and features?

A

Crohn disease

Yersina
gram-negative bacterium, radiographic similar to Crohn’s. resolves quickly, without stricture

TB
-Asymmetric wall thickening of ileocecal valve and
- Cecum and terminal ileum are usually contracted (cone-shaped cecum)
- nb Crohn’s not typical for caecum
-Look for signs of peritonitis/ ascites & caseated nodes
- ** large linear Ulcers with elevated margins **
- Fleischner/umbrella - narrowed TI and open ileocecal valve

Carcinoid
Mesenteric mass (± calcification)/ desmoplastic infiltration of SB mesentery

28
Q
A

Neutropenic Colitis (Typhlitis)

Life-threatening, necrotizing enterocolitis occurring primarily in severely neutropenic patients

Massive mural thickening of cecal ± ascending colon wa
Mucosal hyperenhancement and submucosal edema (marked)

Caecum

29
Q
A

Pyogenic
-Singular - Klebsiella
-Multiple - E.coli
-‘Double targe sign’
-Confluent complex cystic lesions

Candida - Bulls eye

Amoebic
- ‘extra hepatic extension’ - if left lobe needs emergently drained as can rupture into the pericardium
-transient hepatic attenuation difference (THAD) due to thrombophlebitis of portal vein and hyperemia of abscess capsule
- enhancing capsule and hypodense halo of edema

Hydatid
- ‘water lily, sandstorm’
- Large, well-defined, cystic liver mass with numerous peripheral daughter cysts
- Echinococcus

Schistosomiasis is - ‘Tortoise shell’
- Septations hyperdense

30
Q
A

Hepatic Cavernous Hemangioma

US - Hyperechoic with acoustic enhancement
CT - Hypodense (isodense to blood)
MRI - T1 low and T2 High (++ light bulb)

Enhancement - Peripheral nodular arterial enhancement (supplied by hepatic artery)
slow, progressive, centripetal enhancement isodense to vessels

> 10cm = Giant
incomplete centripetal filling of lesion (scar does not enhance)

Haemangioma vs mets

  • delayed imaging and T2 haemangioma is brighter than the spleen
  • So bright can cause T2 shine through on DWI
31
Q
A

FNH

Female predominant .

2nd most common benign lesion after haemangioma

CT/ MRI
- Homogenously arterial enhancement except for central scar.
- blends in imperceptibly on the portal venous-phase
- delayed enhancement of central scar

MRI
-‘Stealth lesion’ - Isointense on t1/t2 to liver parenchyma
**Nb central scar can by hyperintense on T2
- retains gadoxetate **

Sulfur colloid hot*

Nb Small haemangioma can mimic and have rapid filling - peripheral enhanced areas though stay isodense to blood vessels

32
Q
A

Hepatic adenoma

Female (OCP) or Man (steroids)
**Solitary
Multiple = Von Gierke

Can’t reliably differentiate from HCC on imaging.

Heterogeneous
Hyper vascular mass
+/- foci of fat or haemorrhage

Nb Signal drop out as fat

Propensity to bleed - RUQ pain is often the presentation

Doesnt retain Gad like FNH as no functioning bile ductules

33
Q
A

HCC

Look for Liver cirrhosis

AFP elevated (90%)

Often invade the hepatic and portal vein

Arterial hyperenhancement and washout in PV or delayed phases on CT or MR

Heterogenous MR/CT depending on the degree of fatty change, fibrosis, necrosis

34
Q
A

fibrolamellar HCC

Young and non-cirrhotic
Normal AFP
May Ca2+

**‘Central scar’ ** = Doent enhance
scar is T1/T2 dark
Gallium avid (FNH is colloid sulfur)

Heterogeneously enhancing, large, lobulated mass with hypointense central scar and radial septa

35
Q
A

Hepatic angiomyolipoma

Well-circumscribed, mostly (sometimes variable amount) fatty mass

US hyperechoic
CT gross fat
MRI T1 and T2 hyperintense

associated with tuberous sclerosis

36
Q
A

Cholangiocarcinoma

Elderly, male, Painless jaundice

‘Capsular retraction’
Delayed enhancement
Peripheral biliary dilatation

Encasement of the portal or hepatic veins but NO tumour thrombus

Klatskin tumour - is cholangiocarcinoma at the bifurcation of the right and left hepatic ducts.

37
Q
A

biliary cystadenoma of liver

Solitary large, well-defined, unilocular or multiloculated cystic
Mural calcifcation
Enhancement of septa/capsule

CANT differentiate from biliary cystadenocarcinoma

38
Q
A

Primary versus secondary haemochromatosis

Low signal on T1 and T2
loss of signal on the in phase
Increased density on CT

Primary
- Genetic, increased absoprtion of iron
- Liver and pancreas invloved
- Spleen is SPARED

Secondary
- Acquired, Chronic illness, multiple transfusions
- Liver and SPLEEN
- pancreas is spared

MSK
large hook osteophytes involving 2nd and 3rd MCP joints

39
Q

Differences between HIV cholangiopathy and PSC?

A

The intrahepatic duct appearances are difficult to tell apart

PSC
- Extrahepatic stricture’s rarely >5mm
- Has saccular deformities of the ducts

HIV
- Focal strictures of the extrahepatic duct > 2cm and associated with papillary stenosis

40
Q

which type of choledochal cyst is the most common and which type is caroli’s disease?

A

Type 1 - Focal dilatation of the CBD

Type 5 is Caroli’s - Intrahepatic only

Type 2 and 3 are very rare
- 2 = diverticulum of the CBD
- 3 = Choledochocele (into duodenum)

Type 4 is both intra and extrahepatic

  • associated with medullary sponge kidney
41
Q
A

Carolis disease

Intrahepatic only

Carolis disease
- ‘Central dot sign’ - portal vein branch within dilated intrahepatic duct
- associated with medullary sponge kidney, - ADPRD

42
Q
A

Adenomymatosis
- Crystals are intraluminal (within rokitansky-aschoff sinuses)

Cholesteroloisis
- Cholesterol is within the substance of the LAMINIA PROPRIA and associated with polyps

GB wall thickening
intramural cystic spaces containing echogenic foci and comet-tail artifacts

Can be focal (typicallf fundal)
or segmental or diffuse

Focal most common @ fundus. Cant be differentiated from GB cancer.

43
Q
A

Pancreatic Lipomatous Pseudohypertrophy

DDX

CF

shwachman-diamond syndrome
2nd most common cause of pancreatic insufficiency in children
Short stature (metaphyseal chondroplasia)

44
Q
A

Serous cystadenoma

Grandma (older)
Heterogenous mixed density
Microcystic (honeycomb apperance)
Predilection Pancreatic head
Doesnt communicate with the pancreatic duct (IPMNs do)

20% -** classic central scar +/- Ca2+ **

Can be younger patients with VHL

45
Q
A

Mucinous cystic neoplasm

Mother (50s)
Pre-malignant
Predilection Body and tail
No communication with the pancreatic duct (IPMN)
Unilocular + thick spetations
MacroCyctic components >2cm

can have elavated CEA levels (transform to mucinous cystadenocarcinoma)

Peripheral calcification

46
Q
A

side branch and main branch IPMN

Side branch
- small cystic mass, typically head or uncinate process
- < 3cm, benign
- duct can be enlarged if large amounts of mucin are produced

Main branch
- **Diffuse dilatation of the main duct ** excessive mucin production and accumulation
- atrophy of the gland and Ca2+ (DDx chronic pancreatitis)
- higher malignancy risk - resection
- dilatation of the papilla, with bulging of the papilla into the duodenal lumen, secreting thick mucin = seen on ERCP

47
Q
A

Solid Pseudopapillary Neoplasm

Womens between 10-20

Usually, Asian or black

Large at presentation - solid and cystic, heterogenous

predilection for the tail

‘Thick capsule’

48
Q

Polyposis syndromes?

A

FAP
- Hundreds or thousands of polyps may carpet colon. - Hepatoblastomas
- desmoid tumours

Gardner
- Multiple osteomas including - skull, mandible
- poor dentation
-fibromatoses
- desmoid tumours of mesentery and anterior abdominal wall

Turcot
-** medulloblastomas + GBM**
- Thus Hx diarrhoea and seizures

Cowdens
- aka multiple hamartoma syndrome
- **Fibrocystic disease of the breast
- Breast cancer ** (occurs in up to 50%)
- dysplastic cerebellar gangliocytoma

Peutz-jeghers
- multiple hamartomatous polyps (predominantly the small intestine)
- mucocutaneous melanin pigmentation involving the mouth, fingers and toes
- increased risk of many cancers (upper GI, ovary, thyorid, testes, pancreas and breast)

Hereditary non-polyposis colorectal cancer (HNPCC) / Lynch
- 40s/50s with colorectal cancer
- 5 times more common than (FAP
- It is the most common hereditary cause of endometrial cancer

Also Cronklite-canada syndrome
- hamartous polpys in the stomach and colon,
- alopecia or nail atrophy

49
Q

Hypervascular solid pancreatic tumors?

A

Islet cell/Neuroendocrine

associated with MEN -1 and VH L

Functional
- insulinoma - most common (75%), solid, small, benign
- Gastrionoma - associated with MEN. malignant ~ 50%. Causes increased gastric acid/ulcer Zollinger-Ellison

Non-functional
- usually malignant (80%)
- large and metastatic at time of diagnosis
- Ca2+

50
Q
A

Coelaic disease

CT enterography: Evidence of reversed fold pattern, multifocal intussusception

Fold reverseal (jejunum like the ileum, ileum like the jejunum. Decreased number of jejunal folds and increased ileal folds

-Moulage sign - smooth tubular appearance of the jejunum
-Dilatation without fold thickness

Mesenteric lymph nodes (low density) - Fat-fluid levels
Splenic atrophy

Iron def anaemia
associated with idiopathic pulmonary hemosiderosis
Increased risk if bowel wall lymphoma

DDX
Lymphoma
- Thickened ,nodular folds

51
Q

Gallbaldder polyp vs GB malignancy

A

see image

52
Q

appearances of Regenerative and dysplastic nodules?

A

Regenerative nodules (iron)
- Typically, isodense on NECT unless have iron = **siderotic regenerative nodules with are HYPERDENSE **
- Typically, low on T1 and T2
- Do not enhance

Dysplastic (fat, glycoproteins)
- show early arterial uptake but the contrast DOESNT wash out on delayed phase (unlike HCC)
- T1 bright, T2 isointense/low

Differentiate from HCC
- increased T2 signal
- restricted diffusion
- Arterial enhancement and WASHOUT on multiphase postcontrast imaging

53
Q
A

Groove pancreatitis

Form of chronic pancreatitis affecting pancreaticoduodenal groove

Curvilinear soft tissue between pancreas and duodenum

often with cystic degeneration within groove or medial wall of duodenum

54
Q
A

Autoimmune pancreatitis

Sausage-like enlargement of pancreas (with smooth contour and loss of pancreatic lobulations).

Hypoattenuating halo or capsule around pancreas

No pancreatic duct dilatation

Lack of calcifications and fluid collections

Can be focal or diffuse

DDX
Focal AIP can difficut to differentiate from pancreatic carcinoma. MPD dilatation and atrophy in cancer

Chronic pancreatitis
Ductal dilatation and Ca2+

Extrapancreatic imaging findings

IgG4 cholangitis in 90%: May be indistinguishable from primary sclerosing cholangitis
Stricture of common bile duct (CBD) ± intrahepatic ducts with hyperenhancement of duct wall

Renal -
Round or wedge-shaped low-attenuation parenchymal lesions. Diffuse renal enlargement
Perirenal soft tissue rind (mimicking lymphoma)

Retroperitoneal fibrosis, IgG4-related lung disease, and enlarged salivary glands or salivary gland mass

55
Q

Cause of hypervascular liver Mets?

A

melanoma
RCC
Choriocarcinoma /Carcinoid
Thyroid
(MRCT)

Neuroendcorine tumours

56
Q

Causes of splenic cysts?

A

Post -traumatic pseudocyst (80%) **
- no epithelial lining thus false cyst
- mural calcification

True cysts (20%)
- majority are parasitic/hydatid
- nonparasitic = are congenital epidermoid cyst

DDX
- Lymphoma
Homogeneously enlarged spleen, multiple tiny hypodense nodules, or discrete hypodense mass(es)

  • Hemangiomas may be hypervascular on arterial-phase CECT
  • lymphangiomas may be multiloculated with septations
57
Q
A

Pseudomyxoma peritonei

Low-attenuation masses (usually < 20 HU) scattered throughout peritoneum

Thick walls, septa and calcificaiton

‘scalloped appearance’/displace of liver and spleen

Mucocele

Dominant cystic or solid mass often present in right lower quadrant/tip caecum (in expected location of appendix) .

+/- curvillenar calcifcation

Mucin-producing neoplasm of appendix causes appendiceal distention and subsequent perforation with diffuse intraperitoneal spread of mucinous implants

DDx

Peritoneal carcinomatous
- discrete tumour Implants are solid
-Rarely may cause “scalloping”

TB peritonitis
- Ascites and omental/mesenteric fat stranding with symmetric, smooth enhancement and thickening of peritoneal lining
-can be loculated
- look for including low-attenuation mesenteric nodes and thickening of cecum and terminal ileum

58
Q
A

HHT

**Tortuous and prominent hepatic arterial branches **

Dilated hepatic veins and early filling

Arterial phase, mosaic attenuation of the liver with multiple enhancing foci

aka Osler-Weber-Rendu syndrome
Hereditary multiorgan disorder → fibrovascular dysplasia with development of telangiectasias and arteriovenous malformations (AVMs)

59
Q
A

Sigmoid Vovulus

Inverted U shape
Ahaustra
Coffee bean - cleft is double thickenss of opposed bowel loops
Directed toward right upper quadrant (RUQ) or left upper quadrant (LUQ);

Look for -
Gas in proximal small bowel and colon
Abscence of air in rectum

Tend to be older patients
Mx with rectal decompression

60
Q
A

Caecal voluvulus

Dilated, air-filled left upper quadrant or abdominal midline

Haustra

Single, long air-fluid level within cecum (upright or decubitus film)

Moderately distended small bowel, little gas in distal colon

Markedly dilated cecum that appears upside down and backward with ileocecal valve directed laterally

61
Q

CT enterography features of active Crohn’s disease

A

**mucosal hyperenhancement **- most sensitive indicator
but seen in other bowel diseases

most specific sign for chrons -
Prominence of the vasa recta adjacent to the inflamed loop of bowel (comb sign) along with increased mesenteric fat attenuation

wall thickening (thickness >3 mm)

CT enterography to depict extra-enteric disease/complications including
-obstruction
-sinus tract
-fistula and abscess formation

long-standing/inactive features include
-submucosal fat deposition
-pseudosacculation
-surrounding fibro-fatty proliferation
-fibrotic strictures

MR enterography and enteroclysis
- MR enteroclysis was superior to MR enterography in demonstrating mucosal abnormalities.
-MR enteroclysis better bowel distension but not necessarily better diagnostics
-MR enterography is more acceptable to the patient than MR enteroclysis