Leukemia and Lymphoma Flashcards

(47 cards)

1
Q

Leukopenia is a WBC count less than…

A

< 4.5k

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2
Q

leukocytosis is a WBC count…

A

> 11K

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3
Q

This leukemia:

is the most common acute leukemia in adults

Average age is 65 yo

rare and rarely fatal,

A

acute myeloid leukemia (AML)

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4
Q

A 65 yo patient w/ a hx of benzene exposure complains of anemic sxs, neutropenic sxs (fever), bleeding, and ophthalmic changes.

What do you suspect based off this hx?

A

AML

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5
Q

For a pt. you suspect of AML, what should you expect to see on CBC with Diff and in the peripheral smear

A

+ pancytopenia
+ 20% blasts
+ Auer Rods on peripheral smear

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6
Q

For a pt. you suspect of AML, what would a CMP show? What two other labs might help with a dx?

A

elevated creatinine, liver fxn, increased potassium, calcium

elevated Uric Acid and elevated LDH

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7
Q

Can auer rods be seen in disorders other than AML?

A

Yes, they are pathognomonic only of myeloblasts

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8
Q

You suspect a patient has AML.

Labs indicate the following:

+ pancytopenia
+ elevated LDH, Uric Acid
+ elevated calcium and potassium
+ Auer Rods

What test do you want ot order to confirm you dx?

A

bone marrow aspiration and biopsy showing 20% blasts

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9
Q

Induction tx for AML includes what?

A

chemotherapy for 6 mo

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10
Q

consolidation therapy for AML includes what?

A

stem cell transplant

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11
Q

What is a common progression to AML?

A

Myelodysplastic syndromes

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12
Q

This disease is characterized by abnormal cell maturation, and ineffective blood cell production leading to pancytopenia.

it is commonly asymptomatic and found incidentally on CBC

Cure is via bone marrow transplant

It can progress to AML?

A

myelodysplastic syndrome

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13
Q

This disease occurs 12-24 hours after cytotoxic therapy

is associated with high mortality

and occurs when massive tumor cells lyse to release contents (K, PO3, nucleic acid)

A

tumor lysis syndrome

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14
Q

What should you expect to see on labs in tumor lysis syndrome?

A

hyperkalemia, hyperphosphatemia, hypocalcemia, hyperuricemia

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15
Q

how do you treat TLS?

A

prevention, monitor cardiac fx

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16
Q

This leukemia is associated with the BCR-ABL1 fusion gene, the philadelphia chromosome and tyrosine kinase activation…

A

chronic myeloid leukemia (CML)

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17
Q

A 50 yo male pt. presents c the following after routine blood work. Pt. appears asymptomatic:

  • hx of ionizing radiation
  • profound leukocytosis (WBC > 100k)
  • B sxs
  • Splenomegaly
  • fatigue

What do you suspect?

A

CML

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18
Q

When a patient c CML is in blast crisis, what would be present?

A

20% blast cells

fatigue, fever, extramedullary blasts, splenomegally

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19
Q

How do you diagnose a pt. you suspect of CML?

A

identification of philadelphia chromosome or BCR-ABL gene

20
Q

CML can be treated with…

A

Tyrosine Kinase Inhibitors

Monoclonal Abs

Chemo

Allogenic Stem Cell Transplant

21
Q

Complications of CML include…

A

tumor lysis syndrome

hyperleukocytosis

hyperviscosity syndrome

Tx with leukapheresis/plasma exchange

22
Q

A 2 year old male patient of caucasian descent c NF1 presents c. the following…

Hx:
+ Fever, Fatigue, Pallor, Bone pain
+ hx genetic disorders

PE:
+hepatosplenomegaly, nontender LAD

Labs:
+ Neutropenia, anemia, thrombocytopenia
+ elevated LDH

Peripheral smear:
+ 20% lymphoblasts

What do you suspect, and what test do you want to Dx?

A

suspect ALL

Get bone marrow biopsy

23
Q

70-80% of childhood ALL is what subtype?

A

precursor B-Cell ALL

24
Q

Precursor B-Cell ALL has a favorable or unfavorable prognosis?

25
80% of this type of ALL express CD10
Precursor B-Cell ALL
26
What type of ALL has the following features... Hyperleukocytosis at Dx Older age mediastinal mass intramedullary disease
T-Cell ALL
27
This type of ALL is also called burkitt cell lymphoma it presents with CNS sx and bulky extramedullary disease
Mature B-Cell ALL
28
Standard treatment for ALL is...
2 year course of chemotherapy
29
This type of leukemia has the following characteristics... Median age of 70 yo, only adults + B cell lymphocytosis organomegaly Skin changes (leukemia cutis, macules, papules, etc) may be treated with observation if early stage 1
CLL
30
A pt. presents c the following: Painless cervical LAD Mediastinal mass on CXR Pain after EtOH B Sxs Fatigue Pruritus s rash This presentation is concerning for what?
hodgkins lymphoma
31
A patient is positive for the following: supraclavicular LAD splenomegaly hepatomegaly Reed-Sternberg cells. This is concerning for what?
Hodgkins lymphoma
32
You are concerned a pt. may have hodgkins lymphoma. What can confirm the diagnosis? What do you need to stage the disease?
Dx via lymph node biopsy showing + Reed Sternberg cells Get CT/PET to stage
33
Describe the treatment options for HL.
Chemo, very effective Radiation in bulky disease stem cell transplant for relapse or persistent disease
34
A patient c. HL presents with bilateral cervical LAD, bulky disease, distant spread. How should this affect prognosis?
worse prognosis
35
90% of non-hodgkin lymphoma is derived from...
B lymphocytes
36
A pt. presents c. the following on H&P: - Diffuse, painless, persistent LAD - Mediastinal mass - B sxs - Extra lymphatic sites like bone marrow. This is concerning for what?
NHL
37
Diffuse large B cell lymphoma burkitt lymphoma adult t cell leukemia-lymphoma precursor B and T lymphoblastic leukemia/lymphoma These conditions are associated with what...
aggressive NHL B Sxs Elevated LDH, Uric Acid
38
Dx for NHL is done via...
lymph node biopsy CT/PET Bone Marrow aspiration
39
A patient with slow growing indolent NHL is treated with...
radiation alone
40
Aggressive, intermediate or high grade NHL is treated with...
chemo + immunotherapy + autologous stem cell transplant
41
this disease is a malignancy of plasma cells.
multiple myeloma
42
when performing protein electrophoresis on a patient suspicious for multiple myeloma, what you expect ot find?
paraproteins, M-Spike
43
A patient presents c. the following on H & P: Fatigue, back pain, weakness, parasthesia in LE, incontinence, weight loss. What is this concerning for?
multiple myeloma
44
A pt. presents with the following lab findings: M-Spike on protein electrophoresis + bence-jones proteins in urine + lytic lesions and osteoporosis on X-Ray This is concerning for what?
multiple myeloma
45
CRAB stands for what? It is concerning for what disease?
Calcium > 10.5 Renal Insufficiency Anemia Bone Lesions concerning for multiple myeloma
46
Tx of multiple myeloma...
hem/onc combination chemo Iv bisphosphonates to prevent bone loss autologous hemopoietic cell transplant
47
Pt. presents with bone pain in spine and ribs recurrent infections hypercalcemia anemia kidney failure. What does this concern for?
Multiple myeloma. Bones BREAK in multiple myeloma (Bone pain, Recurrent infx, Elevated calcium, Anemia, Kidney failure)