Case studies in Leukemia and Lymphoma Flashcards

1
Q

Myelodysplastic syndromes (MDS) occurs due to age-related acquired genetic damage to?

It is marked by what blood cell conditions?

A

1) Hematopoietic cells

2) Cytopenias and dysmorphic blood cells

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2
Q

What symptoms may we find on physical examination that point towards acute myeloid leukemia?

A

1) Petechiae

2) Conjunctival pallor

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3
Q

What lab values may we acquire that point towards acute myeloid leukemia?

A

1) Elevated WBC

2) Low platelet count

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4
Q

What would a Peripheral blood smear show for suspected acute myeloid leukemia?

A

Large cells with large nuclei and visible nucleoli

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5
Q

What would flow cytometry show for suspected acute myeloid leukemia?

Where would it be highest?

A

1) Myeloid blasts

2) Bone marrow

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6
Q

A patient with AML arising from MDS with have what presentation?

A

1) Anemia
2) Thrombocytopenia
3) Neutropenia

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7
Q

When starting chemotherapy on an AML patient, what should the process be?

A

1) 2 week course based on AML subtype and genetic profile

2) Recheck bone marrow at 2 weeks

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8
Q

What can cause fever in a patient that has AML?

A

Severe neutropenia leading to infection

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9
Q

What do you treat a neutropenic patient with to get their count back up?

A

GM-CSF

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10
Q

What is Induction chemo?

What is Consolidation chemo?

What is Maintenance chemo?

A

1) Initial chemo to induce a remission
2) Intensifying chemo to make sure no cancer cells are left in the body
3) Longer term therapy to maintain the remission and prevent relapse for certain cancers

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11
Q

What symptoms may we find on physical examination that point towards acute promyelocytic leukemia?

A

1) Purpura

2) Conjunctival pallor

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12
Q

What lab values may we acquire that point towards acute promyelocytic leukemia?

A

1) Low WBC
2) Low platelet
3) High PT/aPTT time
4) Low fibrinogen
5) High D-dimer

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13
Q

In Disseminated Intravascular Coagulation (DIC), endothelial injury and anticoagulant dysfunction cause?

A

Widespread thrombin release

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14
Q

What is a significant histological finding seen in acute promyelocytic leukemia?

A

Auer rods

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15
Q

What genetic finding confirms diagnosis of Acute Promyelocytic Leukemia?

A

t(15;17)

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16
Q

In Acute Promyelocytic Leukemia, the leukemic cells express?

What does each do?

A

1) Tissue Factor which activates factor X

2) Annexin II which converts plasminogen into plasmin

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17
Q

Patients with Acute Promyelocytic Leukemia with DIC are immediately treated with?

A

1) Platelet transfusion

2) Factor replacement

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18
Q

What is comprised of the special chemotherapy tailored to Acute Promyelocytic Leukemia?

A

1) Arsenic trioxide

2) All trans retinoic acid (vitamin A derivative)

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19
Q

What are two fatal consequences of Acute Promyelocytic Leukemia with DIC?

A

1) Pulmonary hemorrhage

2) Cerebral hemorrhage

20
Q

What physical findings can be found on exam in patients with chronic myeloid leukemia?

A

Splenomegaly

21
Q

What lab findings can be found in patients with chronic myeloid leukemia?

A

1) Normocytic anemia
2) Very high WBC (leukocytosis)
3) Low Leukocyte Alkaline Phosphatase

22
Q

As WBC count gets closer to 100, what condition should be your first thought?

23
Q

What will the buffy coat look like in a centrifuged sample for a patient with leukemia?

A

Thick buffy coat layer

24
Q

When is positive Leukocyte Alkaline Phosphatase (LAP) staining seen?

A

Leukemoid reactions

25
What does absent LAP staining indicate?
Neoplasm
26
What bone marrow findings do we see in patients with CML?
1) Hypercellularity of white cells 2) Pseudo-Gaucher cells (blue-green macrophages) 3) t(9:22) Philadelphia chromosome
27
In the Philadelphia chromosome, what rearranged gene creates a protein that causes a constitutively active tyrosine kinase?
BCR-ABL
28
What is the treatment for CML? What is its MOA?
1) Imatinib (Gleevec) | 2) Tyrosine kinase inhibitor
29
What do you use to monitor CML? With what testing?
1) BCR-ABL | 2) Fluorescence in-situ hybridization (FISH) or PCR
30
So what defines successful treatment for CML?
1) White count normalizes (Hematologic response) | 2) Negative BCR-ABL PCR (Molecular response)
31
What do we see in the accelerated phase (CML-AP)?
1) Circulating blasts 10-19% 2) Thrombocytopenia 3) Basophilia
32
What do we see in the blast phase (CML-BP), aka “Blast crisis”?
Circulating blasts 20% or higher
33
What symptoms and findings should raise suspicion for malignant lymphadenopathy and should be biposed?
1) Subclavian LAD 2) Fixed, hard LAD 3) Lymph node >4 cm
34
A tender LAD is often categorized as?
Benign
35
Flow cytometry works best for what conditoin?
Non-Hodgkin's lymphoma
36
What is the only way to diagnose Hodgkin Lymphoma? Why?
1) Excision/excisional biopsy | 2) To be able to view diagnostic Reed-Sternberg cells
37
Burkitt lymphoma is an example of a lymphoma that is likely to present with a what type of mass?
Rapidly enlarging mass
38
What is the translation for Burkitt lymphoma? The genes invovled?
1) t(8;14) | 2) IGH/MYC
39
What chemotherapy is used for Burkitt lymphoma with CNS involvement?
Chemo with intrathecal administration
40
What condition causes the patient’s urine output decreases dramatically and there are increases in potassium, serum creatinine, and BUN? It is successfully treated with?
1) Tumor lysis syndrome | 2) Aggressive hydration
41
Involvement of what tissue/system are more likely with this lymphoma than other NHL types?
CNS and bone marrow
42
Pruritus and chest pain from taking a drink are symptoms of what condition?
Hodgkin Lymphoma
43
What is very effective in treating Hodgkin Lymphoma?
Chemo
44
When may a Hodgkin Lymphoma not produce any symptomatology?
When its limited to a mediastinal mass
45
What physical findings can be found in a patient with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL)?
1) Conjunctival pallor 2) Petechiae 3) Axillary and cervical LAD
46
CLL/SLL often presents as? It is found and diagnosed in?
1) Asymptomatic | 2) Peripheral blood
47
If CLL/SLL begins to progress what happens?
1) Bone marrow involvement | 2) Richter’s transformation (transition to high grade lymphoma)