Paper I
2022 February (2019 Scheme) · 100 marks · 180 min

Question

8gm%. A bone marrow examination was ordered the next day.  What is the most likely possibility in such a situation  What are the findings expected in a bone marrow examination  What are the laboratory investigations you will do to arrive at a diagnosis and what are the expected results  What are the complications of this disease (2+3+6+4)

Q310 marksEssays

Answer

This is a continuation of the clinical case in printedNumber 1 of this paper (elderly man with fatiguability, bone pain, decreased urination, pallor, Hb 8 g%, normal TLC/platelets, marked rouleaux formation, ESR 110 mm/1st hour) — the most likely diagnosis being Multiple Myeloma.

Most likely possibility

  • Multiple myeloma (plasma cell neoplasm)

Expected bone marrow findings

  • Increased plasma cells (>10% of marrow cellularity, often much higher)
  • Plasma cells showing atypical/abnormal morphology — binucleation, prominent nucleoli, perinuclear hof loss, eccentric nuclei, “flame cells”
  • Sheets or clusters of plasma cells replacing normal haematopoietic tissue

Laboratory investigations and expected results

  • Serum protein electrophoresis: M-spike (monoclonal band, usually IgG or IgA)
  • Urine Bence Jones protein: Positive (free monoclonal light chains, kappa or lambda)
  • Serum free light chain assay: Abnormal kappa/lambda ratio
  • Skeletal survey/imaging: Multiple punched-out lytic lesions (skull “raindrop skull,” vertebrae, pelvis, long bones)
  • Serum calcium: Elevated (hypercalcaemia from osteolysis)
  • Serum creatinine/renal function: Elevated (myeloma kidney/cast nephropathy)
  • Beta-2 microglobulin: Elevated (prognostic marker)
  • Peripheral smear: Rouleaux formation (as already noted), normocytic normochromic anaemia

Complications of multiple myeloma

  • Renal failure (“myeloma kidney” — cast nephropathy, hypercalcaemia-related nephrotoxicity, AL amyloidosis)
  • Recurrent bacterial infections (functional hypogammaglobulinaemia despite high total immunoglobulin)
  • Pathological fractures (from lytic bone lesions)
  • Hypercalcaemia (weakness, confusion, polyuria, constipation)
  • Hyperviscosity syndrome (bleeding, visual disturbances, neurological symptoms)
  • Amyloidosis (AL type, from light chain deposition)
  • Spinal cord compression (from vertebral involvement/collapse)

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