PACES__Gastroenterology/nephrology Flashcards

(34 cards)

1
Q

Give two possible causes of oral ulceration

A
  1. IBD
  2. SLE
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Give 3 possible causes of macroglossia

A
  1. Hypothyroidism
  2. Acromegaly
  3. Amyloidosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Which immunosuppressant medication causes gingival hypertrophy?

A

Ciclosporin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is Troisiers sign?

A

Palpable lymph nodes in the left supraclavicular fossa indicative of proximal gastric cancer. Most likely adenocarcinoma of the stomach.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Give 6 causes of acanthosis nigricans

A
  1. Hyper/hypothyroidism
  2. Cushing’s syndrome
  3. T2DM
  4. Paraneoplastic syndrome
  5. Acromegaly
  6. Obesity
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the 3 most common causes of CLD in the west?

A
  1. Alcohol
  2. Viral
  3. Metabolic
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Name 7 complications of CLD

A
  1. Portal HTN
  2. UGIB
  3. Ascites
  4. SBP
  5. Hepatorenal syndrome
  6. Hepatopulmonary syndrome
  7. Hepatic encephalopathy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the definition of ESRF?

A

eGFR<15

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Name 3 barriers to transplantation

A
  1. Deep seated infection
  2. Malignancy
  3. Lack of donors
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Name side effects of steroids, ciclopsorin and tacromlimus

A
  1. Steroids: skin thinning, diabetes, proximal myopathy, adipose redistribution
  2. Ciclopsorin: hirsutism, gingival hyperplasia
  3. Tacrolimus: tremor
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the mode of inheritance of APKD? What gene is the defect located on?

A

Autosomal dominant
PKD1 and PKD2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the average age of symptom onset for APKD?

A

~40

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Name 2 common extra-renal manifestations of APKD

A
  1. Hepatic cyst
  2. Intracerebal berry aneurysm
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Name 2 disadvantages of peritoneal dialysis in APKD

A
  1. Risk of infected cyst
  2. Risk of increased peritoneal volume
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What score is used to assess need for liver transplant in chronic liver disease? What score is necessary to be considered for transplant?

A

UK-MELD
49

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the definition of acute liver failure?

A

A multisystem disorder in which a severe acute impairment of liver function with encephalopathy occurs within 8/52 of initial insult. There should be no evidence of underlying chronic liver disease.

17
Q

Name 6 variant syndromes may lead to liver transplantation?

A
  1. Intractable pruritis
  2. Diuretic resistant ascites
  3. Hepatopulmonary syndrome
  4. PCKD
  5. Chronic hepatic encephalopathy
  6. Recurrent cholangitis
18
Q

What values go in to calculating a UK-MLED score?

19
Q

What is the mode of inheritance of HH? What chromosome is the defective gene on and what gene is defective?

A

AR
Chromosome 6
HFE

20
Q

What cause of arthralgia is closely associated with HH?

21
Q

What is the inheritance pattern of hereditary spherocytosis?

22
Q

What is the triad of typical hereditary spherocytosis presentation?

A
  1. Jaundice
  2. Anaemia
  3. Splenomegaly
23
Q

Name 2 complications of hereditary spherocytosis

A
  1. Pigmented gallstones
  2. Aplastic crisis
24
Q

What is the diagnostic test for hereditary spherocystosis? (2 options)

A
  1. EMA binding test
  2. Osmotic fragility test
25
Give 5 crucial aspects of management of hereditary spherocytosis
1. Start folate 2. Consider splenectomy 3. Serial RBC transfusions 4. Pneumococcal and meningococcal vaccinations 5. Prophylactic antibiotics
26
What is the definitive diagnostic test for coeliac disease?
D2 biopsy showing total or sub-total villous atrophy
27
Where do transplanted pancreases typically drain?
Traditionally into the bladder Nowadays into the small bowel
28
What is the score for prognosis in CLD?
Child-Pugh score
29
What are the acute and chronic complications of pancreatitis?
Acute: ARDS, SIRS Chronic PV thrombosis, pseudocyst, compression of adjacent structures
30
What type of stent is used to drain pancreatic pseudocysts? How are pseudocysts accessed?
1. Axios stent 2. Via endoscopy
31
What percentage of pancreas exocrine function must be lost before becoming clinically apparent?
~90%
32
What must be remembered with the faecal elastase test?
It will only be low in moderate to severe disease
33
What electrolyte test is most valuable in assessing pancreas dysfunction?
Magnesium
34
What is the criteria for super urgent transplant in paracetamol overdose?
The King’s College Criteria pH < 7.3 or In a 24h period, all 3 of: INR > 6 (PT > 100s) + Cr > 300mmol/L + grade III or IV encephalopathy