PPQs Flashcards
Elderly woman with C. diff colitis and profuse diarrhoea
Hypovolaemic hyponataraemia
Man with cough, SoB and weight loss. Hyponatraemia, low serum osmolality, urine Na and osmolality were inappropriately normal. Diagnosis?
- SIADH secondary to small cell lung cancer
Low plasma sodium, low urine sodium
- Psychogenic polydipsia
Man who has been in a car accident, raised sodium and plasma osmolality, low urine osmolality
- Cranial diabetes insipidus
Raised Na, low K, HTN but raised renin
- Renal artery stenosis
NOTE: RAISED RENIN MEANS RENAL ARTERY STENOSIS, if this was low would be Conn’s syndrome
Refractory, elevated levels of what ion are an indication for dialysis?
K+
Woman comes in with bitemporal hemianopia, 2cm mass, and a raised prolactin 1400
non functional macroadenomas can compress dopamine stalk and cause raised prolactin, they are most likely to cause visual defects
Woman comes in with no visual change, 4mm mass, and raised prolactin 1400
- Prolactinoma
Raised prolactin, raised TSH, raised T4
TSHoma
NOTE: Raised prolactin, raised TSH, raised T4
calcium high, PTH low
- Bone metastases
Calcium low, PTH low
- Hypoparathyroidism
Blood levels in osteoporosis
Normal
Order of investigations in acromegaly
Serum IGF then OGTT (diagnostic)
Gold line investigation for cushing’s disease
Inferior petrosal sinus sampling, do low dose dexmeth first
24 year old asymptomatic man with isolated rise in unconjugated bilirubin (all other results (ALT, ALP etc normal)
- Gilbert’s
- 22 year old student with two weeks anorexia, fever and malaise – ALT was most elevated, raised ALP + GGT
Viral Hepatitis
NOTE: ALT most elevated indicates viral hepatitis
A 57 year old man presents following hematemesis and is found to have high ALT + GGT, slightly raised ALP, and low Albumin
Cirrhosis
NTOE: albumin low indicates chronic liver disease
Deficiency of which enzyme leads to hyperuricemia?
- HGPRT
Which enzyme regulates the rate limiting step in the haem biosynthesis pathway?
- ALA synthase
enzyme that is raised in mumps
- Amylase-S
High calcium, normal phosphate, low PTH, high ALP, patient feels tired
- Metastatic disease
72 year old with headache: high CA, normal phosphate, normal PTH, high ALP
- Pagets
Baby with seizures: low Ca, low PTH
Hypoparathyroidism (e.g. du to DiGeorge syndrome)
Pt presents with low mood after renal transplant following longstanding renal disease: high Ca, high PTH
Tertiary hyperparathyroidism
10 year old with seizures: low Ca, high PO4, high PTH
Renal osteodystrophy
most common cause of acute pancreatitits
gallstones
Most common cause of chronic pancreatitis
alcohol
Which thyroid cancer most commonly metastasises to the lymph nodes?
Papillary
T1DM with hypoglycaemia, what is the management option if no IV access?
IM glucagon
enzyme that makes monosodium urate in gout, needle shaped aspirate with negative birefringence
- Xanthine oxidase
cause of dark urine with no blood on microscpy
- Myoglobin
Marker for heart failure
- NT-pro BNP
liver enzyme raised in heart attack
AST
PCSK9 inhibitor - evolucumab, what does it halve?
LDL levels
Which molecule takes cholesterol and moves it to liver and steroidogenesis organs?
HDL
Vitamin deficiency that causes megaloblastic anaemia and neural tube defect.
FOLATE - vitamin B9
What vitamin is folate?
B9
What herpes virus is EBV?
HHV4
- Rank the following in order of highest to lowest reticulocyte count
a. Anaemia secondary to low dose myelosuppressive chemotherapy
b. Hereditary spherocytosis
c. ITP
d. Occult GI blood loss
e. Severe aplastic anaemia
Hereditary spherocytosis: This is a hemolytic anemia where the bone marrow responds by producing more reticulocytes to replace the destroyed red blood cells. Therefore, it typically has a high reticulocyte count.
Occult GI blood loss: Chronic blood loss from the gastrointestinal tract stimulates the bone marrow to increase reticulocyte production to compensate for the lost red blood cells. Thus, it would have a moderately high reticulocyte count.
ITP (Immune Thrombocytopenic Purpura): This condition primarily affects platelets, but if there is associated significant bleeding and resultant anemia, the bone marrow would respond by increasing reticulocyte production. However, the reticulocyte count would generally be less than in conditions with direct red cell destruction.
Anaemia secondary to low dose myelosuppressive chemotherapy: Chemotherapy suppresses bone marrow activity, leading to reduced production of all blood cells, including reticulocytes. Thus, the reticulocyte count would be low.
Severe aplastic anemia: In this condition, the bone marrow fails to produce sufficient blood cells, including reticulocytes. Therefore, it has the lowest reticulocyte count.
- 62 y/o woman attends GP with tachycardia and fatigue. FBC chows macrocytic anaemia, thrombocytopenia, and neutropenia. The blood film shows neutrophils have reduced granularity and lobation, and there is no polychromasia. Rank the following in likelihood of being the diagnosis:
a. Aplastic anaemia
b. Autoimmune thrombocytopenic purpura
c. B12 deficiency
d. Chronic lymphocytic leukaemia
e. Myelodysplastic syndrome
Myelodysplastic syndrome (MDS) - MDS often presents with pancytopenia (anemia, thrombocytopenia, neutropenia) and abnormal blood cell morphology, including neutrophils with reduced granularity and lobation. The lack of polychromasia (immature red blood cells) also suggests a problem with bone marrow function typical of MDS.
Aplastic anemia - This condition can also present with pancytopenia, but the blood film in aplastic anemia typically shows very few cells overall, without the specific morphological changes in neutrophils seen in this case.
Chronic lymphocytic leukemia (CLL) - CLL usually presents with lymphocytosis rather than pancytopenia. However, in advanced stages, it can lead to bone marrow failure and pancytopenia. The blood film in CLL typically shows an increased number of mature lymphocytes rather than the described changes in neutrophils.
Autoimmune thrombocytopenic purpura (ITP) - ITP primarily causes isolated thrombocytopenia and would not typically present with anemia and neutropenia or the specific morphological changes in neutrophils.
B12 deficiency - B12 deficiency causes macrocytic anemia and sometimes mild thrombocytopenia and neutropenia. However, it typically presents with hypersegmented neutrophils, not reduced granularity and lobation. Additionally, B12 deficiency usually causes polychromasia due to the ineffective erythropoiesis.
- Rank the cancers below from most to frequent as a cause of death of men in the UK
a. Breast
b. Colon
c. Head and neck
d. Lung
e. Prostate
Lung
Colon
Prostate
Head and neck
Breast
- Rank the following stages in evolution of oesophageal adenocarcinoma
a. High grade dysplasia
b. Adenocarcinoma
c. Low grade dysplasia
d. Reactive
e. Metaplasia
Reactive changes (d) - This stage involves the initial response of the esophageal lining to chronic irritation, such as from gastroesophageal reflux disease (GERD). These changes are non-neoplastic and are characterized by inflammation and reactive cellular alterations.
Metaplasia (e) - In this stage, the normal squamous epithelium of the esophagus is replaced by columnar epithelium with goblet cells, known as Barrett’s esophagus. This is a pre-neoplastic condition and a direct response to chronic irritation and inflammation.
Low grade dysplasia (c) - This stage involves early neoplastic changes in the metaplastic epithelium. The cells show abnormal growth and appearance but are not yet highly atypical or invasive.
High grade dysplasia (a) - This stage is characterized by more severe cellular abnormalities and a higher likelihood of progressing to invasive cancer. The cells exhibit significant atypia and architectural distortion.
Adenocarcinoma (b) - This is the final stage where the dysplastic cells have invaded beyond the basement membrane and formed an invasive malignancy.
- 72 y/o Afro-Caribbean woman is admitted with acute SOB. PMHx includes hypertension and T2DM. She takes Metformin, Atorvastatin, and Amlodipine. O/E BP is 148/96. Auscultation reveals a 3rd heart sound and bibasal crackles, but no murmurs.
Investigations:
Sodium 142
Potassium 3.5
Urea 12.4
Creatinine 126
Rank the following diagnoses from most to least likely:
a. Essential hypertension
b. Cushing’s syndrome
c. Conn’s syndrome
d. Phaeochromocytoma
e. Addison’s disease
Essential hypertension (a) - This is the most common cause of hypertension, especially in an older adult. The patient’s blood pressure is elevated, which can contribute to heart failure (indicated by the third heart sound and bibasal crackles).
Conn’s syndrome (Primary hyperaldosteronism) (c) - This condition involves excessive production of aldosterone, leading to hypertension and hypokalemia. However, the patient’s potassium level is normal, making this less likely but still a consideration due to the hypertension.
Cushing’s syndrome (b) - Cushing’s syndrome can cause hypertension and other metabolic abnormalities. However, it is less common and typically presents with other features such as central obesity, purple striae, and a moon face, which are not mentioned in this case.
Phaeochromocytoma (d) - This is a rare cause of hypertension due to excessive catecholamine secretion from an adrenal tumor. It typically presents with paroxysmal episodes of hypertension, palpitations, sweating, and headache, none of which are mentioned in the history.
Addison’s disease (e) - Addison’s disease typically presents with hypotension, hyponatremia, and hyperkalemia due to adrenal insufficiency. This patient’s blood pressure is elevated, and electrolyte levels are normal, making Addison’s disease the least likely diagnosis.
- Rank the following in order of efficacy at reducing LDL:
a. Atorvastatin
b. Bezafibrate
c. Evolocumab
d. Prednisolone
e. Simvastatin
Evolocumab (c) - Evolocumab is a PCSK9 inhibitor, which significantly reduces LDL levels, typically by around 60% or more. It is among the most potent agents available for lowering LDL cholesterol.
Atorvastatin (a) - Atorvastatin is a high-potency statin, and it can reduce LDL levels by about 40-60%, depending on the dose.
Simvastatin (e) - Simvastatin is a moderate-potency statin, and it can reduce LDL levels by about 20-40%, depending on the dose.
Bezafibrate (b) - Bezafibrate is a fibrate, which primarily reduces triglycerides but has a modest effect on lowering LDL cholesterol, generally around 5-20%.
Prednisolone (d) - Prednisolone is a corticosteroid and does not lower LDL cholesterol; in fact, it can increase LDL levels.
- 55 y/o woman develops dry mouth and eyes alongside fatigue and arthralgia of the small joints in her hands. Investigations:
Urate normal
ESR 64 (raised)
IgG 22 (raised)
Rheumatoid factor 120 (raised)
Anti-CCP antibody 0.9 (negative)
Speckled anti-nuclear antibody titre 1:640 (raised)
Rank the following diagnoses by likelihood:
a. Gout
b. Osteoarthritis and keratoconjunctivitis sicca
c. Osteogenesis imperfecta
d. Primary Sjogren’s syndrome
e. Rheumatoid arthritis
Primary Sjogren’s syndrome (d) - The combination of dry mouth, dry eyes, fatigue, and arthralgia strongly suggests Sjogren’s syndrome. The elevated ESR, IgG, and positive anti-nuclear antibody with a speckled pattern further support this diagnosis. Sjogren’s syndrome often presents with these symptoms and laboratory findings.
Osteoarthritis and keratoconjunctivitis sicca (b) - Osteoarthritis typically presents with joint pain and stiffness, but it does not usually cause systemic inflammation or elevated IgG and ESR. Keratoconjunctivitis sicca (dry eyes) could be present, but it does not explain the other systemic findings.
Rheumatoid arthritis (e) - Although rheumatoid factor is elevated, the negative anti-CCP antibody makes rheumatoid arthritis less likely. RA typically presents with small joint involvement and systemic symptoms, but anti-CCP is a more specific marker for RA.
Gout (a) - Gout usually presents with acute, episodic joint inflammation and is associated with elevated urate levels, which are normal in this case. It does not cause dry mouth and eyes, elevated IgG, or anti-nuclear antibodies.
Osteogenesis imperfecta (c) - Osteogenesis imperfecta is a genetic disorder characterized by brittle bones and frequent fractures. It does not present with dry mouth and eyes, elevated inflammatory markers, or positive autoimmune serology.
- 22 y/o woman presents with mild SLE. Rank the following test results by likelihood of appearing in this case:
a. Absent IgG
b. Low complement C3
c. Positive ANA
d. Positive C3 nephritic factor
e. Positive ds-DNA
Positive ANA (c) - The antinuclear antibody (ANA) test is the most sensitive for SLE, with a positivity rate of over 95% in patients with the condition. It is almost always positive in cases of SLE.
Positive ds-DNA (e) - Anti-double-stranded DNA (anti-dsDNA) antibodies are highly specific for SLE and are present in about 50-70% of patients with the disease. They are often associated with disease activity and severity, but can also be present in mild cases.
Low complement C3 (b) - Complement levels, particularly C3 and C4, can be low in SLE due to consumption during the immune response. This is more commonly seen in active or severe disease but can also be present in mild cases.
Positive C3 nephritic factor (d) - C3 nephritic factor is associated with certain types of glomerulonephritis and is not commonly seen in SLE. It is less likely to appear in a mild SLE case.
Absent IgG (a) - Absence of IgG is not characteristic of SLE. In fact, patients with SLE often have elevated levels of immunoglobulins due to chronic immune system activation. An absent IgG would suggest a different condition, such as a primary immunodeficiency.
- A 20 y/o woman presents w 2 days of dysuria, increased urinary frequency, and suprapubic pain. Rank the organisms by likelihood of being causative:
i. Proteus mirabilis
ii. Acinetobacter baumanii
iii. Candida albicans
iv. Escherichia coli
v. Staphylococcus saprophyticus
Escherichia coli (iv) - E. coli is by far the most common cause of uncomplicated UTIs, responsible for 70-90% of cases.
Staphylococcus saprophyticus (v) - This is the second most common cause of UTIs in young sexually active women, accounting for about 5-15% of cases.
Proteus mirabilis (i) - Proteus species are less common but still a notable cause of UTIs, particularly in individuals with urinary tract abnormalities or those who are catheterized.
Candida albicans (iii) - Candida species are typically associated with fungal infections, and Candida albicans is more likely in patients with indwelling catheters, diabetes, or immunosuppression. It is not a common cause of uncomplicated UTIs in otherwise healthy individuals.
Acinetobacter baumanii (ii) - Acinetobacter species are uncommon causes of community-acquired UTIs and are more typically associated with hospital-acquired infections, particularly in patients with prolonged hospitalization or indwelling catheters.
- A neonate develops meningitis at 36 hours old. Rank the organisms by likelihood of being causative:
i. Escherichia coli
ii. Group B Strep
iii. Cryptococcus neoformans
iv. Pseudomonas aeruginosa
v. Listeria monocytogenes
Group B Streptococcus (ii) - Group B Streptococcus (GBS) is the most common cause of early-onset neonatal meningitis. It is typically acquired during delivery from the mother’s genital tract.
Escherichia coli (i) - E. coli, particularly strains that express the K1 antigen, is another common cause of early-onset neonatal meningitis. It is also acquired from the maternal genital tract during birth.
Listeria monocytogenes (v) - Listeria is a less common cause of neonatal meningitis but is still significant. It can be transmitted vertically from the mother to the neonate during childbirth.
Cryptococcus neoformans (iii) - Cryptococcus is an extremely rare cause of neonatal meningitis and is typically seen in immunocompromised individuals. It is not a typical cause of early-onset neonatal meningitis.
Pseudomonas aeruginosa (iv) - Pseudomonas is a rare cause of neonatal meningitis and is more commonly associated with hospital-acquired infections. It is unlikely in a healthy neonate presenting with early-onset meningitis
- At what temperature can platelets be stored for transfusion for 7 days?
20-24 degrees
Name of LMWH
Enoxaparin
What does this image show?
Reed sternberg cells - owel eyes
- 45 y/o man attends GP with fatigue and easy bruising. He has recently returned from India where he had a self-resolving episode of jaundice and malaise. Blood tests show a pancytopenia with low reticulocytes. What is the most likely diagnosis?
Aplastic anaemia due to parvovirus B19
- What naturally occurring antibody will be in the serum of an A negative person?
Anti-B IgM
- An O negative pregnant woman undergoes amniocentesis. What intervention does this indicate?
Anti-D immunoglobulin
- Venetoclax is a BCL2 inhibitor used for B-cell CLL. Which cellular process does this act on?
Venetoclax acts on the cellular process of apoptosis
- A 55 year old man attends his GP with severe fatigue and back pain. Investigations:
Creatinine 635 (high)
IgG 3.5 (low)
IgM 0.3 (low)
Serum protein electrophoresis – no paraprotein
Kappa light chains 0.9 (low)
Lambda light chain 1970 (very high)
K/L ratio 0.0005 (low)
What is the cause of the renal failure?
Monoclonal gammopathy of renal significance
NOTE: Elevated Creatinine: The elevated creatinine level indicates renal dysfunction.
Low IgG and IgM: While not specific, low levels of immunoglobulins (IgG and IgM) can be seen in disorders associated with dysregulation of the immune system, such as monoclonal gammopathies.
Elevated Lambda Light Chains: The markedly elevated lambda light chain level and very low kappa light chain level, along with a significantly decreased kappa/lambda (K/L) ratio, indicate monoclonal gammopathy.
No Paraprotein Detected: The absence of a detectable paraprotein on serum protein electrophoresis does not rule out monoclonal gammopathy, as some patients with LCPT may not have detectable paraproteins.
- Why is sickle cell anaemia not symptomatic for the first 3 months of life?
sickle cell isn’t symptomatic till > 3months as fetal Hb deosn’t contain beta Hb chains
- Most common cause of constrictive pericarditis in developing world?
Tuberculosis
- What is the most common cause of myocarditis
Viral infection (coxsackie B)
- What is the most common cause of portal vein thrombosis
Cirrhosis of the liver
- What is the most common primary breast cancer?
invasive ductal carcinoma
Most common type of oesophagael cancer in the UK
Adenocarcinoma - Barrets
SCC - smoking - superfical (most common worldwide)
- What is the most likely cause of a mobile mass in a young woman’s breast?
Fibroadenoma (aka breast mouse)
- Which underlying pathology is commonly associated with nephrotic syndrome in adults
Membranous glomerulonephritis
- What is the most common primary tumour of the heart?
Myxoma
- What is the equivalent of a dysgerminoma in a testis?
Seminoma
- Intestinal metaplasia in Barrett’s oesophagus is most commonly due to the presence of which cell?
Simple columnar epithelial cells
- What type of emphysema is associated with smoking and chronic bronchitis?
Centrilobular (centriacinar) emphysema
- Which vascular tumour is associated with HHV8?
Kaposi sarcoma
- Which virus causes encephalitis that particularly affects the temporal lobes?
HSV 1
What is the most common cause of hypocalcaemia in the community? What is the most common cause of hypercalcaemia in the community
Vit D deficiency, Hypereparathyroidism
- Which blood test may confirm a diagnosis of acute pancreatitis?
Diagnosis ofa cute pancreatitis MAY be confirmed by amylase, but definitely confirmed with lipase (more sensitive)
- Deficiency of which plasma protein occurs in patients with movement disorder and liver disease?
Careulopasmin
- Name a hormone that increases urinary phosphate excretion
PTH - phosphate trashing hormone
- Which liver enzyme is associated with obstructive jaundice?
ALP
- Which condition occurs in MEN 1 and 2a?
Parathyroid adenoma
- A patient presents in Addisonian crisis with a systolic BP of 90, which fluid should be given?
0.9% saline
- A hypertensive patient has hypokalaemia and raised aldosterone with suppressed Renin, what is the likely diagnosis?
Conn’s syndrome
NOTE: Raised renin would be renal artery stenosis
- Which vitamin deficiency causes pellagra?
B3 - Niacin
- Which hormone released from fat cells has hypothalamic receptors?
The hormone released from fat cells (adipocytes) that acts on hypothalamic receptors is leptin.
NOTE: Leptin is a hormone primarily synthesized and secreted by adipocytes in response to energy stores in the body. Its levels increase with the accumulation of fat and decrease with fat loss. Leptin acts on receptors in the hypothalamus, specifically in the arcuate nucleus, to regulate appetite, energy expenditure, and body weight.
In the hypothalamus, leptin inhibits hunger (appetite suppression) and stimulates energy expenditure, thereby playing a crucial role in the regulation of body weight and energy balance. Leptin signaling in the hypothalamus helps to maintain homeostasis by modulating food intake and energy expenditure in response to changes in adipose tissue mass and energy stores.
- A 35 y/o woman presents with neck pain worse on swallowing, she had an URTI 2 weeks prior. Investigations show low TSH, and high T3 and T4. Technetium scanning shows low thyroid uptake. What is the likely diagnosis?
Viral thyroiditis - low thyroid uptake
- Which enzyme level or activity should be measured before giving azathioprine?
TPMT
- A young man with periodic fevers has an MEFV mutation. What is the diagnosis?
FMF
- What condition does JC virus reactivation cause in an immunosuppressed person?
PMFL
- CAR-T cells against CD19 treat haematological malignancy of what cell type?
B cell
- Which condition features involvement of kidneys and upper and lower airways, and is associated with cANCA with cytoplasmic staining pattern and specificity for proteinase 3?
Granulomatosis with polyangiitis
- A 3 y/o child with recurrent bacterial and fungal infections has a negative dihydrorhodamine test (does not oxidise). What is the diagnosis?
Chronic granulomatous disease
- CD40 mutation is associated with which immunodeficiency?
Hyper IgM syndrome
- What is the name of a fully differentiated B-cell that makes antibodies?
Plasma cell
- What type of lymphocyte is deficient in an individual with bare lymphocyte syndrome and an HLA class II mutation?
CD4
- A 5 m/o baby has recurrent infections and an IL2RG (interleukin 2 common gamma chain mutation), what is the diagnosis?
X linked SCID
- 29 y/o man returns from charity work in Yemen with profuse watery diarrhoea that “looks like water after you cook rice in it”. What is the causative organism?
Vibrio Cholera
- 43 y/o receiving chemotherapy for leukaemia has ongoing fever and raised inflammatory markers after broad spectrum antibiotic therapy with Meropenem and Amikacin. CT chest shows nodules with surrounding hypoattenuation (halo signs). What is the most likely causative organism?
Aspergillus fumigatus
- 18 y/o man with 1 day history of headache, neck stiffness, and photophobia, but no confusion or other signs of encephalitis. HSV1 detected in CSF PCR. What antiviral treatment would you recommend?
Aciclovir
- 42 y/o man returns from India with high fever and abdo pain but no diarrhoea. Blood cultures grow Gram negative bacilli and Malaria rapid test is negative. What is the most appropriate initial antibiotic therapy?
Ceftriaxone
- Which Herpes virus causes post-transplant lymphoproliferative disorder?
EBV (AKA HHV4)
- 37 y/o woman with hot swollen, painful left knee has Gram positive cocci in clusters on joint aspirate. NKDA and MRSA screen is negative: which narrow spectrum antibiotic is most appropriate here?
Fluclox
- This vaccine-preventable disease presents with headache, fever, and parotid swelling. Can cause epididymo-orchitis in adults and sometimes even meningitis. What is the causative organism?
Mumps orthorubulavirus
- 73 y/o woman with headache, confusion, photophobia, and fever. Gram positive rods are found in her CSF, what is the likely causative organism?
Listeria Monocytogenes
- Name an antibiotic class with concentration-dependent killing and prolonged persistent effects where the goal is to maximise the concentration above the Minimum Inhibitory Concentration (Peak>MIC)
Aminoglycosides
- 78 y/o woman has loose green mucoid stool after a week of I.V. Ceftriaxone. What is the causative organism?
- Clostridium Difficile
- 64 y/o man with poorly controlled T2DM develops periorbital oedema, headache, sinus pain, purulent nasal discharge, and orbital cellulitis. The symptoms started yesterday and he is taken to theatre as an emergency. What anti-fungal should be started immediately?
- Amphotericin B
- Which stage of pregnancy has the highest risk of VTE?
a. 1st trimester
b. Post-amniocentesis
c. 2nd trimester
d. 3rd trimester
e. Post-partum
Post partum
- Which of the following is not usually found in multiple myeloma?
a. Anaemia
b. Humoral immune dysfunction
c. Osteolytic bone lesions
d. Renal impairment
e. Splenomegaly
SPLENOMEGALY
- What cell type mediates acute graft vs. host disease in allogeneic stem cell transplant?
a. Donor B cells
b. Donor T cells
c. Recipient B cells
d. Recipient NK cells
e. Recipient T cells
Donor T cells
- What is the first-line treatment for chronic phase CML?
a. Ibrutinib (Bruton tyrosine kinase inhibitor)
b. Imatinib (ABL 1 tyrosine kinase inhibitor)
c. Rituximab (Anti-CD20 antibody)
d. Thalidomide (Anti-angiogenic)
e. Toilizumab (Anti-IL6 antibody)
Imatinib
- 55 y/o starts Rivaroxoban, what monitoring is required?
a. Anti XA assay
b. aPTT
c. INR
d. No monitoring
e. Platelet count
DOACS need no monitoring
- A PET scan of a Hodgkin lymphoma patient shows involvement of nodes in the supraclavicular fossa, mediastinum, inguinal region, and of the spleen. What stage disease is this?
a. Stage 0
b. Stage 1
c. Stage 2
d. Stage 3
e. Stage 4
Stage 3 - spleen doesn’t count for stage 4
- Which of the following describes the pathophysiology of beta thalassaemia major?
a. Decreased alpha globin chain production
b. Decreased beta globin chain production
c. Decreased gamma globin chain production
d. Increased alpha globin chain production
e. Increased beta globin chain production
beta thalassaemia major has decreased beta globin chain production
- 73 y/o woman presents to GP with fever and productive cough. Auscultation reveals a pleural rub. Her WCC is elevated at 15 and there is neutrophilia. Her haemoglobin is slightly low at 110, CRP is elevated at 98, and platelets are 210. The blood film shows left-shift and toxic granulation. What is the most likely diagnosis?
a. Acute myeloid leukaemia
b. Aplastic anaemia
c. Chronic myeloid leukaemia
d. Infectious mononucleosis
e. Reactive neutrophilia
Reactive neutrophillia, common finding in viral infections such as infectious mononucleosis
- A bleeding patient has a prolonged aPTT and PT, but normal platelets and fibrinogen. Which blood component should they be given?
a. Albumin
b. Anti-D
c. Cryoprecipitate
d. Fresh frozen plasma
e. Platelets
Fresh frozen plasma contains various clotting factors, including factors II (prothrombin), V, VII, VIII, IX, X, XI, and XII, as well as proteins C and S. It is used to correct coagulation factor deficiencies in patients with bleeding disorders or those requiring urgent reversal of anticoagulant effects.
- A 75 y/o woman develops neutropenic sepsis secondary to myelodysplasia. Her FBC is significantly worse than 6 weeks prior, with marked pancytopenia. Blood film shows numerous large cells of primitive appearance. What is the most likely diagnosis?
a. Development of aplastic anaemia
b. Development of iron deficiency
c. Progression to acute myeloid leukaemia
d. Progression to chronic myeloid leukaemia
e. Progression to myelofibrosis
Progression to AML
Myelodysplastic syndromes (MDS) are a group of clonal hematopoietic stem cell disorders characterized by ineffective hematopoiesis leading to peripheral cytopenias. MDS can progress to acute myeloid leukemia (AML) in some cases, particularly when there is increased blast percentage (>20%) in the bone marrow or peripheral blood. The development of neutropenic sepsis and worsening pancytopenia may indicate disease progression to AML.
- Which of the following decreases during pregnancy?
a. Factor 8
b. Fibrinogen
c. Plasminogen activator inhibitor 1
d. Protein S
e. Von Willebrand factor
Protein S decreases in pregnancy
- 55 y/o male smoker on furosemide has the following test results:
Hb 178 (high)
Hct 51% (high
Red cell mass 25 (low end of normal)
Plasma volume 26 (low)
What is the most likely diagnosis?
a. High affinity haemoglobinipathy
b. Polycythaemia vera
c. Primary polycythaemia
d. Relative polycythaemia
e. Secondary polycythaemia
D – low red cell mass and low plasma volume – likely relative polycythaemia due to diuretic use
- A 25 y/o woman with acute leukaemia needs an allogeneic stem cell transplant. She is of mixed Afro-Caribbean and European heritage with one sibling – what is the chance of that sibling being HLA identical?
a. 1:1
b. 1:1000
c. 1:2
d. 1:4
e. 1:100
siblings have 1 in 4 chance of being HLA identical
- Which virus is associated with nasopharyngeal carcinoma?
a. Epstein-Barr virus
b. Hepatitis B virus
c. Hepatitis C virus
d. HHV8
e. HPV16
EBV
- What is the most common type of skin cancer?
a. Basal cell carcinoma
b. Keratoacanthoma
c. Melanoma
d. Metastatic cancer
e. Squamous cell carcinoma
BCC
- An extradural/ epidural haemorrhage is caused by damage to which blood vessel?
a. Berry aneurysm
b. Bridging veins
c. Internal carotid
d. Middle cerebral artery
e. Middle meningeal artery
Middle meningeal artery
- Which type of necrosis is associated with a myocardial infarction?
a. Abscess formation
b. Caseous necrosis
c. Coagulative necrosis
d. Fat necrosis
e. Liquefactive necrosis
coagulative necrosid
- What is the most common glial cell of the CNS?
a. Astrocytes
b. Endothelial cells
c. Ependymal cells
d. Microglia
e. Oligodendrocytes
Astrocytes
- What is the most common cause of mitral valve stenosis?
a. Congenital
b. Infective endocarditis
c. Pulmonary hypertension
d. Rheumatic heart disease
e. Systemic lupus
Rheumatic heart disease
- What is the mechanism behind pulmonary oedema due to liver disease?
a. Decreased osmotic pressure
b. Direct injury to the alveolar wall
c. Increased hydrostatic pressure
d. Indirect injury to the alveolar wall
e. Lymphatic obstructio
Pulmonary edema due to liver disease, known as hepatopulmonary syndrome (HPS), primarily occurs as a consequence of the altered pulmonary vascular dynamics resulting from liver dysfunction. The correct mechanism is:
c. Increased hydrostatic pressure.
In liver disease, particularly in cirrhosis, there is increased resistance to blood flow through the liver, leading to portal hypertension. This elevated pressure in the portal venous system causes congestion and dilation of the pulmonary vasculature, increasing hydrostatic pressure within the pulmonary capillaries. As a result, fluid transudates from the capillaries into the interstitial space of the lungs, leading to pulmonary edema.
- Which of the following occurs near the surface of the brain and is frequently asymptomatic?
a. Glioblastoma multiforme
b. Haemangioma
c. Meningioma
d. Oligodendroglioma
e. Schwannoma
Meningioma
- What is the most common cause of acute respiratory distress syndrome?
a. Aspiration
b. Drug reaction
c. Pancreatitis
d. Sepsis
e. Trauma
Sepsis
- Which valve is classically involved in infectious endocarditis in I.V. drug users?
a. Aortic
b. Mitral
c. Prosthetic
d. Pulmonary
e. Tricuspid
Tricuspid
- Which of the following is a characteristic of hypercalcaemia?
a. Diarrhoea
b. Easy bruising
c. Hypotension
d. Polyuria and polydipsia
e. Tetany
Polyuria and polydipsia
- 25 y/o man brought to A&E with abdominal pain followed by collapse. His blood pressure shows he is in shock and his blood gas results are:
Na+ 120 (low)
K+ 6.2 (high)
HCO3 10.1 (low)
Urea 9.4 (high)
Creatinine 146 (high)
Glucose 2.5 (low)
pH 7.2 (low)
pCO2 3.0 (low)
What is the most likely cause of the abnormal potassium?
a. Renal loss of sodium
b. Vomiting
c. Renal failure
d. Perforated appendix
e. Dehydration
Renal failure
- Which of the following is found in haemolytic jaundice?
a. Raised AST
b. Raised CK
c. Normal bilirubin
d. Pale stools
e. High urobilinogen in urine
High urobilinogen in urine
In hemolytic jaundice, there is an increased breakdown of red blood cells (hemolysis), leading to an elevated production of bilirubin. Bilirubin is a breakdown product of heme from hemoglobin and is normally conjugated in the liver and excreted in bile. However, in cases of increased hemolysis, the liver may become overwhelmed, leading to an accumulation of unconjugated bilirubin in the bloodstream.
As a result of increased bilirubin production, there is an elevation in the levels of bilirubin in the blood (hyperbilirubinemia), leading to jaundice (yellowing of the skin and eyes). Additionally, excess unconjugated bilirubin may be excreted in the urine as urobilinogen, resulting in high levels of urobilinogen in the urine (urobilinogenuria).
- Increased insulin sensitivity causes low plasma glucose, and features in which of the following?
a. Acromegaly
b. ACTH deficiency
c. Cushing’s disease
d. Phaeochromocytoma
e. PCOS
ACTH deficiency
In ACTH deficiency, also known as secondary adrenal insufficiency, there is a deficiency of adrenocorticotropic hormone (ACTH) from the pituitary gland, leading to decreased cortisol production by the adrenal glands. Cortisol is a counter-regulatory hormone to insulin, meaning it opposes the action of insulin and helps maintain blood glucose levels. In the absence of cortisol due to ACTH deficiency, there is decreased gluconeogenesis (glucose production) and increased insulin sensitivity, which can result in lower plasma glucose levels, leading to hypoglycemia.
- Which of the following stimulates receptors in the adrenals and leads to aldosterone release?
a. ACTH
b. Angiotensin 2
c. Calcium
d. Renin
e. Sodium
Angiotensin 2