Bone marrow disorders Flashcards

1
Q

2 classes of bone marrow disorders

A
  1. bone marrow failure

2. myleoproliferative neoplasms

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2
Q

2 types of failure

A
  1. aplastic anemia

2. myelodysplastic syndrome

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3
Q

3 types of myleoproliferative disorders

A
  1. polycythemia vera
  2. essential thrombocythemia
  3. primary myelofibrosis
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4
Q

what is aplastic anemia

A
  • loss of stem cells
  • pancytopenia
  • mostly children and young adults
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5
Q

causes of aplastic anemia

A
  • autoimmune most common

- toxic (chemo, rads)

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6
Q

presentation of aplastic anemia (5)

A
  1. pancytopeina
  2. progressive over weeks to months
  3. anemia - fatigue
  4. leukopenia - infections
  5. thromobpenia - bruising
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7
Q

how to treat aplastic anemia (2)

A
  1. regen. stem cells - immunosuprese: ATG

2. replace stem cells - transplant

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8
Q

what is myleodysplastic syndrome (MDS)

A
  • clonal stem cell disorder
  • takes over marrow
  • progeny are defective
  • cytopenia
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9
Q

presentation of MDS

A
  • cytoenias - slow and progressive

- anemia most common

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10
Q

2 tests for MDS

A
  1. blood film
  2. bone marrow aspirate
    - blast count
    - cytogenetics
    - iron stain
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11
Q

what are 2 risk stratifications of MDS

A

some stay stable and chronic, some rapid to AML

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12
Q

what is treatment for high and low risk MDS

A

low - fix cytopenia to ammeliorte Sx
high - delay or prevent AML
- azitothiprizine
- transplant

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13
Q

what are features of myeloproliferative neoplasms

A
  • clonal stem cell disorders
  • overproduce on lineage
  • may enter fibrotic phase
  • older patients
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14
Q

what is polycythemia vera

A
  • too much RBC
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15
Q

Sx of poly vera

A

think blood leads to

  • H/A
  • visual dist.
  • bleeding
  • pruritis
  • red
  • splenomegaly
  • thrombosis
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16
Q

what is mech of most vera

A

Jak2 self activates without epo and get unrestrained erethropoisis
- see mech

17
Q

4 treats of vera

A
  1. reduce RBCs
  2. phlebotomy
  3. oral chemo
  4. Jak2 inhib
18
Q

what is essential thrombocytopenia

A

too much platelelts

19
Q

Sx of ET

A
  • usually asymtomiatic
  • may bleed
  • thrombosis
  • may spelnomegaly
20
Q

what is ET mech

A

similar to Vera, but instead of EPO, JAK2 without TPO

21
Q

treatment of ET

A
asymptomiatic - observe
if thrombosis 
- ASA
- hydroxyurea
if bleeding
- hydroxurea
22
Q

what is primary myelofibrosis

A
  • marrow replaced by fibrosis
  • extramedularry hematopoesis
  • early: increaed bloods
  • late: decreased
23
Q

3 diagnositic tests

A
  1. marrow and blood - dry tap!
  2. JAK2 in 75%
  3. CALR in 25%
24
Q

4 treatments

A
  1. transfusions
  2. splenectomy - risky
  3. stem cell transplant - can be cure
  4. JAK2 inhib.
25
Q

see cases

A

if you will