Chronic Enteritis, Alimentary Lymphoma Flashcards

1
Q

Prolif and inflamm bowel diseases

A

Infiltrative enteropathies- usually unknown aetiology and pathogenesis

Granulomatous enteritis

MEED: multisystemic eosinophilic epitheliotropic disease

Lymphocytic-plasmacytic enteritis

Prolif enteropathy

Alimentary lymphosarcoma

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2
Q

Prolif and inflamm bowel diseases: tests and plan of action

A

History

Phys exam

Blood haem and biochem

Urinalysis

Faecal: worms and culture

Abd (thoracic) US

Abdominocentesis: cyto and bacto

Oral glucose tolerance test

Biopsy: rectal, intestinal, liver, kidney

Laparoscopy, laparotomy

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3
Q

Prolif and inflamm bowel diseases Phys exam:

A

Malabs and maldigestion: this is why we do oral glucose

Chronic weight loss

Parameters may be normal (apart from BCS)

Chronic Dx

Ventral edema (because of protein loss)

Tissue mass in rectum (tumours in the abd?)

SI abnormalities could impact LI function

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4
Q

Prolif and inflamm bowel diseases lab tests

A

No typical abnormalities to be looking out for!!

Anaemia- normocytic and normochromic (caused by chronic inflamm in this case)

Neutrophilia

Hypoproteinaemia

Hypoalbuminaemia

Abdominocentesis: usually not diagnostic!! in case of abd tumout only a 50-60% chance the sample will contain tumour cells

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5
Q

Prolif and inflamm bowel diseases: US

A

Thickened walls or segments of walls

Dilation

Tissue mass

Could help localize btw small and large

Abd fluid: quantity and quality

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6
Q

Prolif and inflamm bowel diseases: rectal biopsy

A

Simple- biopsy forceps but results could be contradicting!!

Diagnosis in only 50%

Laparoscopy/laparotomy could be more useful

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7
Q

Prolif and inflamm bowel diseases: functional intestinal tests

A

Only for carbs

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8
Q

Oral glucose tolerance tests

A

Gives info on SI abs!!

  • fast for 12-16 hrs
  • 1g/kg glucose in 20% soln(via NG tube)
  • Measure blood prior to glucose admin and every 30 mins until 180 mins
  • NB times are 90 mins and 180 mins: peaks
  • Normal: >85% elevation until 120 mins
  • Partial malabs: 15-95% elevation
  • Total:<15% elevation

Sometimes results contradicting e.g if delayed abs or delayed gastric emptying

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9
Q

D-xylose absorption test

A

V. similar to glucose but less impacted by hormones therefore more reliable!!

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10
Q

Granulomatous enteritis

A

young,2-3 yrs

Standardbreds

Mycobact avium?? Aluminium?

Granulomatous sensitivity reaction- where the antigen could be feed, parasite or bacteria

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11
Q

Granulomatous enteritis clinical signs

A

Malabs

Enlarged mesenteric ln’s- rectal palp

Normal or decr TP, hypoalbuminaemia

WBCs may increase or decr slightly

Sometimes, increased biliary enzymes (ALKP and GGT)

rarely Dx

Anaemia

**Rectal biopsy!

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12
Q

Granulomatous enteritis Therapy

A

Corticosteroids- improves the clinical signs but doesn’t impact long term prognosis

Surgery in localised lesions

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13
Q

MEED- multisystemic eosinophilic epitheliotropic disease

A

aetiology unknown- hypersensitivity, parasite??

Eo infiltration of: GIT, liver, pancreas, ln’s and skin

Eosinophilic: gastroenteritis, granulmatosis, dermatitis

BUT systemic eosinophilia is rare!! i.e rarelt in the blood, therefore must take biopsy for diagnosis

More common than granulomatous enteritis

Young standard and thoroughbreds

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14
Q

MEED- multisystemic eosinophilic epitheliotropic disease: Clinical signs

A

Dx

Hyperkeratosis of stomach

Lesions in SI: prox duo try and take biopsy with scope, dist ileum can only take biopsy via surgery

Granulomatous lesions and ulcers

Fibrosis of Colon

Skin: exudative derm and ulcerative coronitis

Abs tests: DELAYED peak conc

Biochem: Hypoalbumin, incr bile enzymes as before with granulomatous enteritis

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15
Q

MEED- multisystemic eosinophilic epitheliotropic disease: diagnosis and treatment

A

Biopsy: rectum, skin, liver, lymph nodes- if Eo infiltration in all of them then poor prognosis

Therapy: Corticosteroids, AB’s, larvicides

Guarded prognosis

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16
Q

Eosinophilic enterocolitis

A

Differs from the other conditions! don’t confuse with gastroenteritis

Idiopathic

Not multisystemic

Usually no malabs therefore normal BCS

Often diagnosed during colic surgery

Bight red, v inflammed segmental lesions in the int wall- may be able to perform resection, treat with corticosteroids after surgery. if not, treat with NSAID’s

Fair prognosis

17
Q

Lymphocytic-plasmacytic enteritis

A

Rare

Inflamm cell infiltration

No specific signs

Rectal biopsy

Treatment is ineffective

Guarded prognosis

18
Q

Sidenote:

A

It is NB to change diet with all of these diseases

Hay/grass ad lib

More freq and smaller feeds

Oil- can provide E

19
Q

Proliferative Enteropathy

A

This is the only one where there is a known cause!!

Weanlings 3-8mnths (because weaning is stressful)

Predisp: prev AB therapy, overcrowding

LAWSONIA IC!!

  • Obligate IC
  • in crypts of ep of jejunum and ileum- causes tissue prolif!
20
Q

Proliferative Enteropathy: Clinical Signs

A

Lethargy, fever

Sudden weight loss

VENTRAL EDEMA: because loss of protein

Colic signs

Dx in 50%

Dull, rough haircoat

These signs may not always be present

21
Q

Proliferative Enteropathy: Diagnosis

A

Abd US: V thickened small intestinal walls- almost no lumen!!

History, age and clinical signs

Severe hypoalbuminaemia

Faecal PCR

Serology: IMPA

22
Q

Proliferative Enteropathy: lab findings

A

Leucocytosis

Hypoalbuminaemia and proteinaemia

Hyperfibrinogenaemia

Maybe: hyponatraemia, kalaemia, chloraemia

elevated CK

23
Q

Proliferative Enteropathy: treatment

A

AB’s for 2-4 weeks

  • Erythomycin and rifampin
  • Azithro, clarithro
  • Oxytet, Doxy
  • Metronidazole
  • Chloramphenicol

Supportive therapy:

Fluids, electrolytes, colloids, plasma

NSAIDS if fever (give also Ranitidine in younger or omeprazole)

Good prognosis!

24
Q

Alimentary Lymphosarcoma

A

Lymphoma= most common neoplastic condition of haemolymphatic system!!

4 anatomical forms: General, intestinal, mediastinal and dermal

Lymphocytic leukemia is rare

Typically btw 5-10 yrs (alimentary 2-4 yrs)

Unknown aetiology

Often chronic and progressive but could manifest acute signs

Lymphocytosis is rare

25
Q

Alimentary lymphosarcoma: clinical signs

A

Malabs

Weight loss

Enlarged mesenteric lymph nodes: rectal exam

US: thickened intestinal walls

Anaemia

Neutropenia or neutrophilia

Thrombocytopenia

Normal/elevated TP

Hypoalbuminaemia or hyperglobinaemia– losing albumin BUT incr globulins! therefore TP stays the same

26
Q

Alimentary lymphosarcoma: Diagnosis

A

Rectal biopsy, abdominocentesis (38-50%)

Diagnostic laparotomy, biopsy

27
Q

Alimentary lymphosarcoma: treatment

A

Immunosupp drugs or chemo

28
Q
A