Multiple Myeloma and Lymphoid Leukemias Flashcards

1
Q

B-lymphocyte general

A

Recognize epitopes of antigens by way of antibody molecues on their surface
First produce IgM
Isotype switching (IgG later)

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2
Q

Immunoglobulin structure

A

2 heavy chains - greater molecular weight, have Fc that is recognized
2 light chains - lighter

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3
Q

Define monoclonal gammopathy

A

Pathological clonal expansion of a single B or plasma cell leading to the excessive production of a homogeneous monoclonal immunoglobulin or a polypeptide subunit of the immunoglobulin

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4
Q

Define paraproteinemia

A

Implies that there is a structural abnormality in the immunoglobulin (ie incomplete Ig)

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5
Q

M-protein

A

Monoclonal protein

Does not imply anything structurally about the molecule other than its homogeneous nature

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6
Q

Cryoglobulins

A

Abnormal proteins that precipitate at temperatures below body temperature

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7
Q

Define multiple myeloma

A

Clonal origin: malignancy of B lymphocyte plasma cell lineage
Arises in bone marrow
Systemic disease
Production of immunoglobulin

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8
Q

Incidence and Signalment of Multiple myeloma

A

Rare in cats, not found in bone; usually liver and spleen

More common in dogs, tends to cause bone lesions and is found in marrow

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9
Q

Pathology and natural behavior of multiple myeloma

A
Immunoglobulin production
- M component
- Paraprotein
- Usually complete Ig
 . Just light chains Bence Jones
 . Just heavy chains heavy chain disease
- Cryoglobulins insoluble <37 degrees Celsius
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10
Q

Sequelae of M component

A
Infection
- Decreased production of normal Ig
- Immunologic cripples
Hypersensitivity syndrome
- Increased total protein
- Hypervolemia
Organ or bone infiltration with neoplastic cells
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11
Q

Hyperviscosity syndrome

A
Heart failure
- Increased perfusion pressure and hypervolemia lead to cardiomyopathy
- Myocardial hypoxia
Neuro signs
- Poor perfusion
- Seizure, lethargy, abnormal mentation
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12
Q

Renal failure

A
High protein content in filtrate
Tubular obstruction - Bence Jones proteinuria
Amyloidosis
Ascending pyelonephritis
Tumor infiltration
Decreased perfusion
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13
Q

Ophthalmic abnormalities

A

Dilated and tortuous retinal vessels
Retinal hemorrhage
- Acute hemorrhage

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14
Q

Hemorrhagic diathesis

A

Decreased platelet adhesion
Interference with coagulation cascade and fibrin polymerization
Consumption of coagulation factors
Myelophthisis and thrombocytopenia

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15
Q

Other signs of multiple myeloma

A
Severe skeletal pain
Pathologic fracture
Spinal cord compression
Myeloma induced osteolysis
- Osteoclast activation
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16
Q

Hx in MM

A

Nonspecific signs: weakness, PU/PD, pain, lethargy, inappetence
More specific signs: Epistaxis, gingival bleeding, blindness
- Compressive lesion/fracture
- Neuro abnormalities

17
Q

MM Criteria

A

Hyperglobulinemia and monoclonal gammopathy (tick-borne diseases are polyclonal)
>10-20% plasma cells in bone marrow or >5% neoplastic cells
Immunoglobulin light chain (Bence-Jones) proteinuria (never done)
Radiographic evidence of multifocal osteolytic lesions

18
Q

Diagnostic tests

A
CBC
- Anemia, thrombocytopenia, leukopenia
Chem panel
- Hyperglobulinemia
- Hypercalcemia
- Renal failure
Urinalysis and culture
- UTI
19
Q

Monoclonal gammopathies

A
Multiple myeloma
Primary macroglobulinemia
B cell chronic lymphocytic leukemia
B cell lymphoma
Extramedullary plasmacytoma
Plasma cell leukemia
Idiopathic of "of unknown significance" (MGUS)
20
Q

Hyperglobulinemia

A
Elevation in globulins (not specific)
- Divided into alpha 1, alpha 2, beta, and gamma
 . Acute phase proteins
Separation of proteins
- Molecular weight and charge
- Gamma globulin peak
 . Immunoglobulins
 . Polyclonal versus monoclonal
21
Q

Diagnostic tests

A
Bone marrow aspirate
- 5% plasma cells normal
- >10% plasma cells supports MM
Urine
- Bence Jones proteins
 . Dipstick NOT reliable
Survey rads
- Axial skeleton
22
Q

Prognostic factors

A

Reported negative prognostic factors

  • Hypercalcemia
  • Bence Jones proteinuria
  • Extensive osteolytic bone lesions

Don’t be a fortune teller

23
Q

Therapies directed at complications

A
Hyperviscosity syndrome
- Fluid therapy
- Plasmapheresis
Infections
- Antimicrobials
Malignant bone pain
- Analgesics
- Bisphosphonates
- Fx stabilization
- Coarse-fractionated radiation therapy
24
Q

Conventional therapies

A
Alkylating agents
- Cyclophosphamide
- Melphalan
Steroids
- Prednisone
- Dexamethasone
25
Q

Felines

A

Myeloma related disorder

Survival not as good

26
Q

Lymphocytosis

A

True lymphocytosis
- Chronic inflammation/infection
. Viral infection elicits transient lymphocytosis
- Neoplasia
. Lymphoid leukemias
PARR
- Polymerase chain reaction for antigen receptor rearrangements
- Diagnostic test to assess “clonality” of lymphocytes

27
Q

Acute lymphoblastic leukemia

A
Associated with cytopenias
Special stains to differentiate cell of origin
- Lymphoid versus myeloid
All w/ LN involvement vs LSA w/ leukemia
- Which is bigger disease
- Treat the same
CD34+ is a negative prognostic factor
Cell counts <30,000 do better
28
Q

Acute vs chronic leukemia

A

Chronic: a lot of normal looking lymphocytes
Acute: crazsy cells

29
Q

Chronic lymphocytic leukemia

A
Prolonged survival (>2 y)
Usually incidental finding
Start oral chlorambucil and pred
- Organ involvement
- Cytopenias
- Lymphocytes >80,000