Lecture 10: Leukemia and Lymphoma Cases Flashcards

1
Q

What is Myelodysplastic Syndrome?

A
  • age-related acquired genetic damage to hematopoietic cells marked by cytopenias and dysmorphic RBCs
  • considered pre-leukemic
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2
Q

What are Gram (+) cocci and Gram (-) rods we should be concerned about getting an infection from if in a hospital? What is a common fungal infection and what stain is used to see it?

A

Gram (+) - staphylococcus/streptococcus

Gram (-) - E. Coli/pseudomonas

Fungus –> Candida (silver stain)

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3
Q

How is Candida Sepsis treated?

A

voriconazole and amphotericin B

  • replace any central caths that caused the infection
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4
Q

What is a diagnostic finding and a confirmatory finding of Acute Promyelocytic Leukemia?

A

diagnostic - Auer Rods (in circulating blasts)

confirmatory - positive for t(15;17)

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5
Q

What molecules are expressed by Acute Promyelocytic Leukemia cells?

A

express Tissue Factor (activates Factor X) and Annexin II receptors (convert plasminogen into plasmin)

  • both HIGHLY expressed on APL cells
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6
Q

What is the specialized chemotherapy treatment given to patients who suffer from Acute Promyelocytic Leukemia?

A

ATO - arsenic trioxide

ATRA - all-trans retinoic acid (Vitamin A derivative)

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7
Q

What are two life-threatening outcomes of APL?

A

massive cerebral and pulmonary hemorrhage

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8
Q

What does the LAP score tell us about WBCs?

A

positive LAP staining (red/blue) is seen in REACTIVE conditions = Leukemoid RXN

absent LAP staining = abnormal myelocyte population –> NEOPLASM

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9
Q

What are Pseudo-Gaucher Cells?

A
  • macrophages that blue-green cytoplasm typically seen in CML
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10
Q

What does Imatinib (Gleevec) do?

A
  • tyrosine kinase inhibitor (controls ATP-dependent processes by binding where ATP should and blocks it from activating the kinase)
  • pts. with Philadelphia chromosome t(9;22) have this tyrosine kinase problem
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11
Q

How can we test for the Philadelphia chromosome?

A

Cytogenics, FISH, PCR

  • PCR is the most sensitive (shows 1 in 100.000 cells vs 1/20 for cytogenics and 1/200 in FISH)
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12
Q

Hematologic Response vs Molecular Response

A

HR - where white cell count begins to normalize

MR - negative for BCR-ABL PCR

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13
Q

Why is monitoring CML so important?

A

CML can progress to Accelerated phase (10-19% blasts, thrombocytopenia, basophilia)

AP can progress to Blast phase (circulating blasts are 20% or higher)

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14
Q

What are 4 common findings with Chronic Myeloid Leukemia?

A
  1. HIGH WBC count (mature granulocytes/LAP negative)
  2. Splenomegaly
  3. Hypercellular bone marrow
  4. Philadelphia chromosome
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15
Q

What are 3 things that are suspicious for metastatic lymph node cancer?

A
  1. subclavian LAD
  2. fixed and hard LAD
  3. lymph node is > 4cm
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16
Q

What is the only biopsy method that can diagnose Hodgkins lymphoma? What is the diagnostic cell that we are looking for?

A

Excision Biopsy (also best way to diagnose lymphoma)

  • looking for Reed-Sternberg cells (look like owls)
  • fine needle aspiration/needle biopsy not enough
17
Q

What is Tumor Lysis Syndrome and what problems can it cause?

A
  • when bulky tumors breakdown due to chemotherapy and dump their metabolic products
  • efflux of potassium and uric acid crystal buildup can lead to arrythmias and acute renal failure
18
Q

What lymphoma is likely to have a rapidly enlarging mass?

A

Burkitt Lymphoma

  • CNS and bone marrow involvement MORE likely with this lymphoma than other NHL
  • CNS involvement = INTRATHECAL chemotherapy (get chemotherapeutics into CSF via Lumbar Puncture)
19
Q

What is Hodgkins Lymphoma?

A

neoplastic lymphoid proliferation with scattered B-derived Reed Sternberg cells in an ABUNDANT background of T lymphocytes, eosinophils, and other inflammatory cells

  • chemotherapy VERY effective
20
Q

What are the 3 typical ways that Hodgkins Lymphoma presents?

A

lymphadenopathy, constitutional symptoms (“B” symptoms), or incidentally on chest x-ray

21
Q

What is Chronic Lymphocytic Leukemia also known as and how does it typically manifest?

A

also known as Small Lymphocytic Lymphoma

  • peripheral disease is typically what manifests (monoclonal B cells) –> typically diagnostic of what is happening in LNs