hepatobiliary 3: more cholangitis, hepatic lipidosis, etc. Flashcards

1
Q

Lymphocytic Cholangitis cause

A
  • Cause unknown
  • Immune mediated?
  • Transient infection causing immune stimulation and hepatic inflammation?
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2
Q

Lymphocytic Cholangitis history

A

Often lengthy history of intermittent clinical signs, slowly progressive

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3
Q

Lymphocytic Cholangitis signalment

A

– any age, breed, sex

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4
Q

Lymphocytic Cholangitis Clinical signs

A
  • Clinical signs of long-term, low grade illness
    > Weight loss, decreased appetite, vomiting, PU/PD, lethargy
    >Possible icterus
    > Intermittent signs – might be BAR on presentation
  • Concurrent illness (pancreatitis, IBD) can be apparent
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5
Q

Lymphocytic Cholangitis: Presentation on PE

A
  • Poor body condition
  • Hepatomegaly
  • Ascites in 1/3 of cats (high protein fluid)
  • Possible signs of hepatic encephalopathy
  • Pyrexia not common
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6
Q

Lymphocytic Cholangitis: CBC

A

CBC generally normal
* Can see mild non regenerative anemia

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7
Q

Lymphocytic Cholangitis: biochem? vs neutrophilic cholangitis?

A
  • Increased ALT and/or ALP in ~50%
  • Hyperbilirubinemia ~ 30%
  • Hyperglobulinemia ~40-50%
  • Hypoalbuminemia ~ 10-30%
  • ALT and bilirubin tend to be of lower magnitude elevations than neutrophilic cholangitis
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8
Q

Lymphocytic Cholangitis: abdominal fluid

A
  • Can be moderate to marked
  • High protein content, small lymphocytes/inflammation
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9
Q

Aside from lymphocytic cholangitis, What’s another differential for high globulins, low albumin, abdominal effusion (high protein)?

A
  • Feline infectious peritonitis (FIP)
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10
Q

Lymphocytic Cholangitis: radiographs

A
  • Hepatomegaly, ascites evident on
    radiographs
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11
Q

lymphocytic cholangitis ultrasound findings

A

possible findings:
* Normal to coarse hepatic echotexture
* Abdominal lymphadenomegaly
* Ascites
* Gall bladder and biliary tracts: normal or dilated tracts, sludge GB
* Concurrent pancreatitis / enteropathy

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12
Q

Lymphocytic Cholangitis Clinical features can overlap with:

A

FIP, hepatic lymphoma, neutrophilic cholangitis

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13
Q

lymphocytic cholangitis Definitive diagnosis requires

A

Definitive diagnosis requires biopsy
* Portal lymphocytic infiltration
* Ductopenia
* Peribiliary fibrosis

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14
Q

Lymphocytic Cholangitis: Treatment

A

Supportive care:
* Hospitalization and nutritional support might be required
* Antiemetics, appetite stimulant
* Abdominocentesis if marked ascites (comfort)

If signs of HE:
* Lactulose, metronidazole

If signs of coagulopathy or biopsy considered: * Vitamin K
()
* Prednisolone 1-2 mg/kg/day
> No difference in outcome: 1 mg/kg/day versus 2 mg/kg/day in one study
* Ursodiol
> Can combine with prednisolone
> One small study – shorter survival when ursodiol used instead of prednisolone

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15
Q

Lymphocytic Cholangitis: Prognosis

A
  • Long term
    > Monitor liver values, clinical signs
    > Consider tapering prednisolone to ~1 mg/kg if starting higher
  • Complications not common
  • Reported survival times 2-3 years, but small studies
    > No cure, recurrence possible
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16
Q

Hepatic Lipidosis predisposing factors

A
  • Negative energy balance usually the predisposing factor
  • Clinically, 2-14 days of anorexia precedes HL
  • Obesity can predispose
17
Q

primary vs secondary hepatic lipidosis - what are they and which is most common?

A

PrimaryHL:
* Healthy animal has decreased access to food / palatable food, decreased intake secondary to stress

Secondary HL (most common):
* Anorexiasecondarytounderlyingdisease
* E.g., pancreatitis, diabetes mellitus, primary hepatobiliary disease, IBD, neoplasia

18
Q

Hepatic Lipidosis: Pathophysiology, definition

A
  • Negative energy balance alters lipid metabolism
  • Triglycerides accumulate in liver
  • Defined by triglycerides in >80% of hepatocytes; >50% increase in liver weight
  • Functional impairment of liver, intrahepatic cholestasis
  • Nutritional deficiencies caused by anorexia can be important in lipid metabolism
    > Methionine, carnitine, taurine
    > Arginine can contribute to encephalopathy
19
Q

Common underlying or concurrent diseases for hepatic lipidosis

A

> Pancreatitis, diabetes mellitus, primary hepatobiliary disease, IBD, neoplasia

20
Q

Hepatic Lipidosis: signalment and risk factors

A
  • Any age, breed; often middle-aged to older
  • Risk factors: obesity, stressful event/illness
21
Q

Hepatic Lipidosis Clinical signs & examination

A
  • Lipidosis and inciting event can have similar signs
  • Icterus, vomiting
  • Signs of acute hepatic loss = encephalopathy (ptyalism in cats!)
  • Hepatomegaly, loss of muscle mass but retaining fat
22
Q

Hepatic Lipidosis: Diagnosis
- enzymes

A
  • Elevated bilirubin in almost all cases
  • Elevated ALT, AST, ALP very common
    > ALP elevation especially significant in cats (very short half-life, and no steroid-induced ALP in this species)
  • GGT often not elevated with purely HL
    > Could be elevated with concurrent biliary disease
  • Markers of liver dysfunction
    > Decreased urea most commonly (~50% of cases)
23
Q

Hepatic Lipidosis: Diagnosis
- electrolytes

A
  • Electrolyte derangements (low K, P, Mg)
24
Q

Hepatic Lipidosis: Diagnosis
- CBC

A
  • CBC: anemia common
25
Q

Hepatic Lipidosis: Diagnosis
- coagulopathy?

A

common

26
Q

Laboratory abnormalities for hepatic lipidosis can reflect what?

A

can reflect underlying disease
* E.g., elevated lipase with pancreatitis

27
Q

Hepatic Lipidosis: Diagnosis
- radiographs

A

Radiographs can show hepatomegaly

28
Q

Hepatic Lipidosis: Diagnosis
- ultrasound

A
  • Large hyperechoic liver
  • Signs of underlying disease
29
Q

Hepatic Lipidosis: Diagnosis usually based on?

A
  • Diagnosis usually based on history, clinical presentation, labwork and imaging
    > Not specific
30
Q

Hepatic Lipidosis: how to make a definitive diagnosis

A

Definitive diagnosis can be made:
* Liver cytology yielding lipid (can mask other disorders)
> Ill cats tend to accumulate lipid in liver
* Biopsy
> Often not ideal candidates for anaesthesia, biopsy

31
Q

Hepatic Lipidosis: Treatment

A
  • Supportive care
    > IV fluids and electrolyte correction
  • Nutritional support is cornerstone of treatment
    > Often nasogastric or nasoesophageal tube initially
    > Esophagostomy tube under anesthesia when more stable
    > Ideal diet high in protein, moderate in lipid, lower carbohydrate
    > Small frequent meals, gradual increase to meet RER
  • Vitamin K for potential coagulopathy
  • Consider antioxidant & nutraceuticals
    > SAMe, l-carnitine, Vitamin B12, taurine
    > Caution if too many oral medications
  • Treatment of underlying disorders
    > E.g., analgesia with opioids if pancreatitis
32
Q

Hepatic Lipidosis: Prognosis

A
  • Very good prognosis with nutritional support and absence of serious underlying disease
33
Q

Elevated neutrophils, pyrexia, liver enzyme activity
- differentials?

A
  • Neutrophilic cholangitis
  • Pancreatitis
34
Q

Elevated ALP (ALP&raquo_space; GGT) differentials?

A
  • Hepatic lipidosis
  • Cholangitis
  • Pancreatitis