HemeOnc Flashcards

1
Q

What are some RBC morphogies we may see on the boards?

A

Spherocytes- autoimmune/drug-induced
Schistocytes- DIC, TTP
Bite cells- G6PD deficiency

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2
Q

What are the endpoints of an MTP?

A

Hemodynamic stability and adequate tissue oxygenation
Hgb 7-9
INR <1.5x normal
Plts 50-100k
fibrinogen >150

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3
Q

What are the platelet targets for various procedures?

A
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4
Q

What are some of the buzzwords for leukemias?

A

AML: gingival hyperplasia, rash, LAD
APL: bleeding, thrombosis (DIC, hyperfibrinolysis)
ALL: LAD, organomegaly, CNS, bone pain, tumor lysis
TCell leukemia: hypercalcemia, bone lesions

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5
Q

What are the features of APL differentiation syndrome?

A

15-25% of patients treated with ATRA, 2-47days post treatment
Due to cytokine release, increased APL adhesion (beta2 integrins)
Fever, leukocytosis, pulm infiltrates, effusions, rapidly improves with dexamethasone

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6
Q

How is hyperleukocytosis treated?

A

Leukopheresis, dexamethasone, cranial irradiation

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7
Q

How is TLS prevented and treated?

A

Low risk: fluid status and look at labs for allopurinol?
Intermediate risk: 7 days allopurinol and crystalloids
High risk: rasburicase (unless G6PD deficiency), crystalloid
Febuxistat in allopurinol hypersensitivity

Rasburicase in established TLS
HD for refractory cases

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8
Q

When to consider NSGY versus radiation for brain mets?

A
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9
Q

How is spontaneous splenic rupture managed?

A

Embolization. US has 90% specificity for splenic rupture

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10
Q

What are some side effects of dasatinib?

A

Second generation TK inhibitor
Cytopenias, pleural effusions, bleeding (decreases platelet function)

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11
Q

Recall shapes of TEG results and what they mean

A
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12
Q

What complications can be triggered by chimeric antigen receptor Tcell treatment?

A

Cytokine release syndrome
will see fever, multiorgan dysfunction, shock and hypoxemia
Tx with anti IL-6 (tocilizumab)

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13
Q

How is refractory TTP treated?

A

PLX, steroids, rituxumab, and caplacizumab (vWF monoclonal antibody fragment)

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14
Q

What are the features of vaccine-induced immune thrombocytopenia?

A

IgG antibodies that recognize platelet factor 4 but with different epitpoe than HIT. 5-10 days post adenovirus vector vaccine
Will have thrombocytopenia around 50, has disproportionate cerebral/splanchinic involvement compared to HIT
Can still use heparin despite the similarities with HIT

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15
Q

What is the Pelger-Huet anomaly signify on peripheral smear?

A

Neutrophils with fewer lobes than normal.
Seen in COVID, leukemia, myelodysplasia, myxedema, malaria, or drugs. May also be inherited

Iron deficiency can cause hypersegmentation FYI

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16
Q

In hyperleukocytosis, is SpO2 or PaO2 more accurate?

A

SpO2, as leukocytes in blood gas sample use up oxygen

17
Q

In hemorrhagic shock, is whole blood or parts preferred?

A

Parts, 1:1:1 ration is equal to 2:1:1

18
Q

How do steroids help in treating hypercalcemia

A

Decreases extrarenal calcitriol production (lymphoma/myelomas)
Increase renal excretion, inhibit osteoclastic absorption