Multiple myeloma pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Multiple myeloma arises from post-germinal center B lymphocytes, that are normally involved in production of human immunoglobulins. Development of multiple myeloma is the result of multiple genetic translocation between the immunoglobulin heavy chain gene and oncogenes which leads to dysregulated multiplication of plasma cells. On microscopic histopathological analysis, abundant eosinophilic cytoplasm, eccentrically placed nucleus, and russell bodies bodies are characteristic findings of multiple myeloma.

Pathogenesis

• Multiple myeloma arises from post-germinal center B lymphocytes, that are normally involved in production of human immunoglobulins.
• Malignant plasma cell infiltrates haemopoietic locations such as the red bone marrow where they interfere with the production of normal blood cells.
• Distribution of multiple myeloma mirrors that of red marrow in the older individual, and thus this is mostly encountered in the axial skeleton and proximal appendicular skeleton:

1. vertebrae (most common)
2. ribs
3. skull
4. shoulder girdle
5. pelvis
6. long bones
7. extra skeletal structures (extraosseous myeloma): rare

• Abnormal antibodies are produced in multiple myeloma and are deposited in various organs around the body leading to multiple complication such as nephropathy,polyneuropathy, and cardiomyopathy.
• Production of cytokines (especially IL-6) by malignant plasma cells in multiple myeloma causes much of their localised damage, such as osteoporosis. The produced cytokines also increase angiogenesis and create a microenvironment in which the malignant plasma cells can thrive.
• Multiple myeloma may result in renal failure due to either glomerular deposition of amyloid or tubular damage from excretion of light chains called Bence Jones proteins. This can manifest as Fanconi syndrome (type II renal tubular acidosis).
• Immune deficiency occurs in multiple myeloma as the majority of the antibodies are ineffective monoclonal antibodies produced by malignant plasma cell. </ref>

Genetics

• The immune system keeps the proliferation of B cells and the secretion of antibodies under tight control. When chromosomes and genes are damaged, often through rearrangement, this control is lost.
• Often, a promoter gene moves (or translocates) to a chromosome where it stimulates antibody gene to overproduction.
• This genetic mutation results in dysregulation of the oncogene which is thought to be an important initiating event in the pathogenesis of multiple myeloma.
• The genes involved in pathogenesis of multiple myeloma include heavy chain gene (on the chromosome 14, locus 14q32), chromosome 13, and oncogenes (often 11q13, 4p16.3, 6p21, 16q23 and 20q11).
• A familial predisposition to myeloma exists. Hyperphosphorylation of the paratarg proteins, a tendency which is inherited in an autosomal dominant manner, appears a common mechanism in these families. This tendency is more common in African American patients with myeloma and may contribute to the higher rates of myeloma in this group.

Gross Pathology

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  Vertebras in multiple myeloma 
   (Image courtesy of Melih Aktan M.D.)
  

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  Calvarium in multiple myeloma. 
    (Image courtesy of Melih Aktan M.D.)
  

Microscopic Pathology

On microscopic histopathological analysis, multiple myeloma is characterized by the following:

• Abundant eosinophilic cytoplasm.
• Eccentrically placed nucleus.
• Clock face morphology of the nucleus due to chromatin clumps around the edges.
• Russell bodies which are eosinophilic, large (10-15 micrometres), homogenous immunoglobulin-containing inclusions.
• Dutcher bodies which are PAS stain +ve intranuclear crystalline rods.

• Shown below is a series of microscopic images seen in multiple myeloma:

• 

  Multiple Myeloma slide showing plasma cells with large nucleus and scant cytoplasm

• 

  Bone marrow aspiration in multiple myeloma.
  (Image courtesy of Melih Aktan M.D.)

• 

  Bone marrow biopsy in multiple myeloma.
  (Image courtesy of Melih Aktan M.D.)

• 

  Bone marrow in multiple myeloma.
  (Image courtesy of Melih Aktan M.D.)

• 

  Bone marrow in multiple myeloma.
  (Image courtesy of Melih Aktan M.D.)

References

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