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PA H4 | Macrocytic Anemias & B12/Folate — Practice Quiz

Practice 12 questions · Untimed · Unlimited attempts

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Q1 PA15.2 1 pt

A 54-year-old woman presents with progressively worsening fatigue, a sore, red tongue, and tingling in both feet. Her CBC shows Hb 7.2 g/dL, MCV 118 fL, and WBC 4.1 × 10⁹/L. Peripheral smear reveals macro-ovalocytes and neutrophils with 6-lobed nuclei. Serum B12 is 78 pg/mL (normal >200). Serum folate is normal. Which single additional investigation is MOST specific for confirming the underlying etiology of her B12 deficiency?

A Serum methylmalonic acid (MMA)
B Anti-intrinsic factor antibodies
C Schilling test (part I alone)
D Serum homocysteine
E Bone marrow biopsy

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Q2 PA15.1 1 pt

Intrinsic factor (IF), secreted by gastric parietal cells, is essential for B12 absorption. At which anatomical site does the IF–B12 complex bind to a specific receptor to enable absorption?

A Duodenum
B Proximal jejunum
C Terminal ileum
D Proximal ileum
E Caecum

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Q3 PA15.2 1 pt

A peripheral blood smear from a patient with macrocytic anaemia is shown. The key findings are oval macrocytes (macro-ovalocytes) and a neutrophil with 7 nuclear lobes. Which of the following is the MOST likely diagnosis?

A Iron-deficiency anaemia
B Megaloblastic anaemia
C Haemolytic anaemia
D Aplastic anaemia
E Myelodysplastic syndrome (MDS)

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Q4 PA15.3 1 pt

A 38-year-old vegan man presents with fatigue, glossitis, and MCV 122 fL. Serum B12 is low; serum folate is normal. Laboratory testing shows markedly elevated serum methylmalonic acid (MMA) and mildly elevated homocysteine. Which metabolic pathway explains the elevated MMA in B12 deficiency?

A B12 is required as a cofactor for methionine synthase, converting homocysteine to methionine; its absence blocks this step and MMA accumulates
B B12 (as adenosylcobalamin) is required for methylmalonyl-CoA mutase; its absence causes methylmalonyl-CoA to accumulate as MMA
C B12 deficiency impairs the conversion of propionyl-CoA to succinyl-CoA via a folate-dependent pathway, producing MMA
D Absent intrinsic factor prevents conversion of methylmalonyl-CoA in the stomach, causing systemic MMA accumulation

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Q5 PA15.2 1 pt

A 68-year-old woman with a history of total gastrectomy 5 years ago presents with fatigue and a haemoglobin of 8.1 g/dL, MCV 110 fL. Serum B12 is 60 pg/mL. Which mechanism BEST explains her B12 deficiency?

A Loss of dietary B12 intake due to post-gastrectomy food aversion
B Absent intrinsic factor due to removal of all gastric parietal cells
C Blind loop syndrome causing bacterial B12 consumption
D Terminal ileal damage secondary to anastomotic complications
E Increased B12 urinary losses due to altered renal handling

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Q6 PA15.3 1 pt

A patient has MCV 105 fL with macrocytic anaemia. Serum B12 is 180 pg/mL (borderline low). Serum folate is normal. Serum MMA is 0.28 μmol/L (normal <0.4). Serum homocysteine is 14 μmol/L (normal <15). Which is the MOST appropriate conclusion?

A B12 deficiency is confirmed; begin intramuscular B12 immediately
B Folate deficiency is the cause; check red cell folate
C Functional B12 deficiency is unlikely; investigate other causes of macrocytosis
D Subacute combined degeneration is imminent; urgent MRI spine required
E Homocystinuria must be excluded; request urine amino acids

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Q7 PA15.1 1 pt

A 35-year-old pregnant woman at 28 weeks gestation presents with fatigue and pallor. CBC: Hb 9.4 g/dL, MCV 108 fL, platelets 142 × 10⁹/L. Serum folate is markedly reduced; serum B12 is normal; MMA is normal; homocysteine is elevated. Which statement BEST explains why folate demands are increased in pregnancy?

A Renal folate wasting increases due to glomerular hyperfiltration in pregnancy
B Foetal growth requires rapid cell division in placenta and foetal tissues, dramatically increasing folate demand for DNA synthesis
C Increased gastric acid in pregnancy destroys dietary folate before it can be absorbed
D Oestrogen competitively inhibits intestinal folate transport, reducing absorption by 60%

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Q8 PA15.2 1 pt

A 62-year-old man with a 30-year history of heavy alcohol use presents with MCV 104 fL. His peripheral smear shows round macrocytes but NO hypersegmented neutrophils and NO macro-ovalocytes. Serum B12 and folate are both normal. LFTs show elevated GGT and AST. Which is the MOST likely cause of macrocytosis in this patient?

A Occult folate deficiency not detected by serum assay
B Non-megaloblastic macrocytosis due to alcoholic liver disease
C Autoimmune haemolytic anaemia causing reticulocytosis
D Hypothyroidism secondary to alcohol-related autoimmune disease
E Myelodysplastic syndrome caused by chronic alcohol toxicity

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Q9 PA15.2 1 pt

A 45-year-old woman is found to have B12 deficiency on routine screening. She has no neurological symptoms. She is vegetarian but not vegan and eats eggs and dairy products regularly. Anti-parietal cell antibodies are weakly positive; anti-intrinsic factor antibodies are negative. Serum B12 is 142 pg/mL. What is the MOST likely cause of her B12 deficiency?

A Classical pernicious anaemia with established gastric atrophy
B Dietary insufficiency due to lacto-ovo-vegetarian diet
C Food-cobalamin malabsorption (gastric achlorhydria/hypochlorhydria)
D Crohn's disease affecting the terminal ileum
E Fish tapeworm (Diphyllobothrium latum) infestation

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Q10 PA15.3 1 pt

A 58-year-old man known to have pernicious anaemia presents to the emergency department with acute onset of bilateral leg weakness, loss of vibration sense at the ankles, and a positive Romberg sign. His B12 injections were stopped 18 months ago when he 'felt better.' Hb is 10.2 g/dL, MCV 116 fL. Which condition BEST explains his neurological findings?

A Peripheral neuropathy due to folate deficiency
B Subacute combined degeneration of the spinal cord
C Wernicke's encephalopathy from nutritional thiamine deficiency
D Multiple sclerosis presenting with posterior column symptoms
E Cerebellar degeneration due to autoimmune paraneoplastic syndrome

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Q11 PA15.3 1 pt

A laboratory workup on a 48-year-old woman with macrocytic anaemia returns: serum B12 = 120 pg/mL (low), serum folate = normal, MMA = markedly elevated, homocysteine = markedly elevated. A second patient has: serum B12 = normal, serum folate = low, MMA = normal, homocysteine = markedly elevated. Which statement about the biochemical differences between these two patients is CORRECT?

A Both patients have identical biochemical defects because both pathways converge on homocysteine
B Patient 1 (B12 deficient) has elevated MMA because the adenosylcobalamin-dependent pathway is impaired; Patient 2 (folate deficient) has normal MMA because folate does not participate in the MMA pathway
C Patient 2 (folate deficient) will also develop elevated MMA over time as folate deficiency worsens
D Elevated MMA in Patient 1 is caused by impaired thymidylate synthesis, not a cofactor deficiency

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Q12 PA15.1 1 pt

A second-year MBBS student studying a bone marrow aspirate from a patient with B12 deficiency notes very large erythroid precursors with open, lacy (sieve-like) nuclear chromatin, even though the cytoplasm is well haemoglobinised. The granulocyte precursors are also very large ('giant metamyelocytes'). Which cellular mechanism BEST explains these findings?

A Increased erythropoietin driving accelerated erythroid differentiation without adequate iron
B Nuclear–cytoplasmic dissociation: DNA synthesis is impaired (nuclear maturation lags), while RNA/protein synthesis and haemoglobin production proceed normally (cytoplasmic maturation is preserved)
C Mitochondrial dysfunction causing failure of haem synthesis in late erythroblasts
D Apoptosis of late normoblasts producing large pale ghost cells on the aspirate

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