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PA H11 | Plasma Cell Dyscrasias (Multiple Myeloma) — Practice Quiz

Practice 10 questions · Untimed · Unlimited attempts

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Q1 PA20.3 1 pt

Multiple myeloma is best defined as a malignant neoplasm of:

A Immature B-lymphoblasts in bone marrow
B Terminally differentiated plasma cells secreting a monoclonal immunoglobulin
C Follicular centre B-cells in lymph nodes
D Natural killer cells in peripheral blood

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Q2 PA20.3 1 pt

Which set of findings constitutes the 'CRAB' criteria used to diagnose symptomatic multiple myeloma?

A Cough, Renal failure, Anaemia, Bone pain
B HyperCalcaemia, Renal insufficiency, Anaemia, Bone lesions
C HyperCalcaemia, Raised ESR, Albuminuria, Bone lesions
D Coagulopathy, Renal failure, Autoimmunity, B-symptoms

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Q3 PA20.3 1 pt

A 62-year-old man presents with back pain and fatigue. Serum protein electrophoresis (SPEP) shows a sharp, narrow peak in the gamma region. Which additional test best characterises the specific heavy- and light-chain class of this abnormal protein?

A Serum immunofixation electrophoresis
B Serum protein electrophoresis repeated with higher voltage
C Urine dipstick for proteinuria
D Flow cytometry of peripheral blood

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Q4 PA20.3 1 pt

Bence-Jones protein found in the urine of multiple myeloma patients consists of:

A Intact monoclonal IgG molecules filtered by the glomerulus
B Free monoclonal light chains (κ or λ) filtered by the glomerulus
C Albumin lost due to glomerular basement membrane damage
D β2-microglobulin shed from plasma cell surfaces

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Q5 PA20.3 1 pt

A peripheral blood smear from a suspected myeloma patient shows red cells arranged in long chains resembling a stack of coins. This finding is called:

A Spherocytosis
B Rouleaux formation
C Schistocytosis
D Target cell formation

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Q6 PA20.3 1 pt

Bone marrow examination is central to the diagnosis of multiple myeloma. The minimum percentage of clonal plasma cells required to diagnose myeloma (in the presence of end-organ damage) is:

A >2%
B >5%
C >10%
D >25%

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Q7 PA20.3 1 pt

Skeletal X-rays in multiple myeloma classically show:

A Sclerotic (dense) bony lesions throughout the axial skeleton
B Periosteal new bone formation (sunray appearance) at tumour margins
C Multiple 'punched-out' lytic lesions, most prominent in skull, spine, pelvis, and ribs
D Bilateral symmetric osteoarthritis of large joints

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Q8 PA20.3 1 pt

In multiple myeloma, serum β2-microglobulin (β2M) is used primarily as a:

A Diagnostic marker to confirm monoclonality
B Prognostic marker — elevated levels correlate with high tumour burden and worse survival
C Treatment response marker replacing serum-free light chains
D Screening test to distinguish MM from reactive plasmacytosis

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Q9 PA20.3 1 pt

A 58-year-old woman is found incidentally to have a serum M-protein of 1.8 g/dL (IgG-κ) on electrophoresis done for fatigue. Bone marrow biopsy shows 7% plasma cells. Haemoglobin is 13.2 g/dL, calcium is normal, renal function is normal, and skeletal survey shows no lytic lesions. The most accurate diagnosis is:

A Symptomatic multiple myeloma requiring immediate chemotherapy
B Monoclonal gammopathy of undetermined significance (MGUS)
C Waldenström macroglobulinaemia
D Smouldering multiple myeloma (asymptomatic myeloma)

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Q10 PA20.3 1 pt

A 70-year-old man with known multiple myeloma presents acutely with severe headache, blurred vision, and epistaxis. Blood film shows marked rouleaux. He has an IgM paraprotein of 5.8 g/dL on immunofixation (a finding atypical for standard MM). This clinical picture suggests complication by:

A Hypercalcaemic crisis requiring bisphosphonate infusion
B Hyperviscosity syndrome, most typically associated with Waldenström macroglobulinaemia and IgM paraprotein
C Acute renal failure due to cast nephropathy
D Spinal cord compression from a vertebral plasmacytoma

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