W4 lect7: myeloma and CLL Flashcards

1
Q

WHAT IS lymphoma?

A
  1. malignancy involving lymphoid cells
    - B-cell or T-cell, B-cell by far most common
  2. Involve lymph nodes and/or secondary lymphoid tissues (SLO), (spleen, thymus, Peyer’s patch, mucosal tissues)
  3. Spread to:
    * Bone marrow
    * Peripheral blood spill over
    * Other organs
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2
Q

what is leukamia?

A
  1. malignancies of the bone marrow +/- peripheral blood involvement
  2. > 20% malignant white cells in peripheral blood or
    bone marrow
  3. Clinical features due to:
    * Bone marrow infiltration (replacement of normal
    haemopoiesis)
    * High white cell counts (abnormal white cells)
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3
Q

why does classification matter?
*Leukaemia & lymphoma

A
  1. Disease will be detected by clinician in blood or LAD (most of the time)
  2. Requires appropriate supportive management, referral, and work-up
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4
Q

why does classification matter?
* Lymphoid vs myeloid

A
  • Flow cytometry on blood?
  • FISH studies?
  • BMAT?
  • Supportive investigations?
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5
Q

why does classification matter?
chronic vs acute

A
  • Aggressive vs indolent
  • Urgency of investigation and referral
  • Management until patient is transferred
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6
Q

what is the chronic lymphocytic leukaemia/ lymphoma?

A
  • Clonal (malignant) proliferation and accumulation of mature B-cells
  • Involving blood/BMA/lymph nodes
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7
Q

what is the epi. of CLL?

A
  • Most common adult leukaemia.
  • ~1-3 / 100 000 per annum (USA).
  • Disease of the elderly, most frequent >70 years.
  • Increased in males.
  • Genetic basis - seen more commonly in America and
    Europe&raquo_space; Asia and Africa. Seen in all population groups
    in South Africa.
  • Familial cases well described.
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8
Q

what is the M:F ratio?

A

1.9: 1

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9
Q

what is the clinical presentation of CLL?

A
  1. Asymptomatic with incidental raised WCC – due to lymphocytosis
    * Up to 50% patients
    * WCC > 10 x 109/L
    * Abs lymphocyte > 4 x 10
    9/L
  2. Other features of leukaemia/lymphoma:
    * +/- BMF symptoms – anaemia/neutropaenia/thrombocytopaenia
    * +/- LAD or HSM – Mass (abdominal or other)
    * +/- B-symptoms (more aggressive disease or due to splenomegaly
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10
Q

HOW do we investigate or diagnose?

A
  • cytometry
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11
Q

what myeloma/ plasma cell myeloma?

A
  • Plasma cell malignancy
  • Monoclonal plasma cells
  • Proliferate in bone marrow
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12
Q

where do we look for plasma cells?

A

bone marrow aspirate and trephine

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13
Q

what are the supportive investigations?

A
  • To look for end organ damage
  • Renal function
  • FBC
  • CMP
  • Skeletal survey
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14
Q

where do we look for paraprotein?

A
  • urine
  • blood
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15
Q

conquences of paraprotein collection?

A
  1. Overabundance monoclonal paraprotein (M protein)
    * Renal impairment
  2. Destruction of bone
    * Hypercalcaemia
  3. Displacement of other hematopoietic cell lines
    * Anaemia
    * Neutropaenia
    * Thrombocytopaenia
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16
Q

diagnoses of mml

A
  • blood screening
  • bone pain is the most prevalent presenting symptom
  • CRAB criteria: hypercalcaemia, renal imparment, anaemia, bone lesions
17
Q

diagnosis/ work- up?

A
  1. Serum protein electrophoresis
  2. Urine protein electrophoresis
  3. Baseline investigation for end organ damage
    * Renal function
    * FBC
    * CMP
    * Skeletal survey
  4. BMAT – for diagnosi
18
Q

Second commonest haematologic cancer in adults
after non-Hodgkin lymphoma

A

multiple myeloma

19
Q

common systoms assoc. with multiple myeloma

A
  • bone pain
  • weakness, malaise
  • anemia, bleeding
  • hypercalcemia
  • spinal cord compression
  • pathologic fractures
  • infections
  • neuropathies
20
Q

treatment of mml

A
  • drugs
  • bone marrow transplantation