Multiple Myeloma

MULTIPLE MYELOMA


MULTIPLE MYELOMA

  • It is a malignant neoplasm derived from plasma cells.

Pathology:

  • The neoplasm characteristically affects flat bones i.e.,
  1. the pelvis
  2. vertebrae
  3. skull, and
  4. ribs

It may occur as a:

  1. solitary lesion (plasmacytoma),
  2. multiple lesion (multiple myeloma),
  3. extra-medullary myelomatosis or diffuse myelomatosis.
  • The lesions are mostly small and circumscribed.
  • The bone is simply replaced by tumour tissue and there is no reactive new bone formation.
  • Grossly, the tumour is soft, grey and friable.
  • Microscopically, it consists of sheets of closely packed cells.
  • Typically, the tumour cells have an eccentric nucleus with clumped chromatin.

Clinical features:

  • The tumour affects adults above 40 years of age.
  • Men are affected more often than women.
  • Usual presentation is that of multiple site involvement.
  • Common presenting complaint is increasingly severe pain in the lumbar and thoracic spine.
  • Pathological fractures, especially of the vertebrae and ribs may result in acute symptoms.
  • The patient is weak, and will have loss of weight.
  • Neurological symptoms may result if the tumour presses on the spinal cord or the nerves in the spinal canal.

Investigations:

Radiological examination:

Characteristic radiological features are as follows:

  • Multiple punched out lesions in the skull and other flat bones.
  • Pathological wedge collapse of the vertebra, usually more than one, commonly in the thoracic spine.
  • Diffuse, severe rarefaction of bones.
  • Erosions of the borders of the ribs.

Other investigations:

Blood:

  1. Low haemoglobin,
  2. high ESR (usually very high),
  3. increased total protein,
  4. A/G ratio reversed,
  5. increased serum calcium,
  6. normal alkaline phosphatase.
  • Urine: Bence Jones proteins are found in 30% of cases.
  • Serum electrophoresis: Abnormal spike in the region of gamma globulin (myeloma spike) is present in 90% of cases.
  • Sternal puncture: Myeloma cells may be seen.
  • Bone biopsy from the iliac crest, or a CT guided needle biopsy from the vertebral lesion may show features suggestive of multiple myeloma.
  • Bone scan: This may be required in cases presenting as solitary bone lesion, where lesions at other sites may be detected on a bone scan.
  • Open biopsy: An open biopsy from the lesion may sometimes be required to confirm the diagnosis.

Treatment:

  • It consists of control of the tumour by chemotherapy, and splintage to the diseased part by PoP, brace etc.
  • Radiotherapy plays a useful role in cases with neurological compression, localised painful lesions, fractures and soft tissue masses.

Chemotherapy:

  • Melphalan is the drug of choice.
  • It is given in combination with Vincristine, Prednisolone, and sometimes Cyclophosphamide.

Exam Important

  • Most common primary malignant bone tumor Multiple myeloma.
  • Commonest site of lytic lesion in multiple myeloma is Vertebral column.
  • Bone marrow plasmacytosis in multiple myeloma is characteristically more than 30%.
  • Multiple myeloma will lead to increased viscosity of blood.
  • Multiple punched out lesions on X-ray is seen in Multiple myeloma.
  • Russell bodies are found in Multiple Myeloma.
  • Increased ESR is seen in Multiple myeloma.
  • Increased serum calcium is seen in Multiple myeloma.
  • The immunoglobulin least commonly involved in Multiple Myeloma is IgD.
  • The immunoglobulin most commonly involved in Multiple Myeloma is IgG.
  • The most common translocation seen in patients with Multiple Myeloma is t(11;14).
  • Excretory urography should be cautiously performed in Multiple myeloma.
  • Drugs used in chemotherapy of multiple myeloma is Melphalan is the drug of choice 
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