EXAM #2: CANCER & HEMATOLOGICAL MALIGNANCY Flashcards

1
Q

What is the definition of a Leukemia?

A
  • Unregulated growth of WBCs (leukocytes) in the bone marrow

Note that this can leads to either increases or decreases of WBCs in the peripheral blood AND bone marrow failure i.e. pancytopenia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the broad definition of a Lymphoma?

A

Discrete tumor masses in the lymph nodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the difference between a Leukemia and Lymphoma?

A

Leukemia= neoplasm of the bone marrow

Lymphoma= neoplasm of the lymph nodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the general difference between an acute and chronic leukemia?

A

Acute= will kill within weeks without treatment

Chronic= patient may survive for years without treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What do the terms myeloid, myelogenous, and myeloproliferative refer to?

A

Tumors involving the:

  • Granulocytes
  • RBCs
  • Platelets

And their progenitors*

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What do the terms lymphoid, lymphocytic, lymphoblastic, and lymphoproliferative refer to?

A

Tumors involving the:

  • B-cells
  • T-cells
  • NK-cells

And their progenitors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the two types of acute leukemia?

A
Acute myeloblastic (AML) 
Acute lymphoblastic (ALL)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the root of symptoms for patients with ALL and AML?

A

Pancytopenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the difference between ALL-B and ALL-T?

A

Cell of origin is B vs. T cell in “Acute Lymphoblastic Leukemia”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the general feature of all AMLs?

A

Undifferentiated myeloblasts accumulating in the bone marrow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the most common acute leukemia in adults?

A

AML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the basis for the FAB categorization of AML?

A

Appearance of cells under microscope

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the basis of the WHO categorization of AML?

A

Pathology, cytogenetics, and molecular characteristics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the two types of ALL? Which is more common?

A

B-ALL* (B-cell)
T-ALL (T-cell)

This is the most common type of all ALL cases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the most common acute leukemia in children?

A

ALL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the difference between a myeloproliferative neoplasm and AML?

A

Myloeproliferative neoplasm can lead to AML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

List the major myeloproliferative neoplasms.

A

1) Polycythemia vera
2) Essential thrombocytpoenia
3) Primary myelofibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is polycythemia vera?

A

RBC overproduction i.e. Hct >55%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is the mutation associated with polycythemia vera?

A

JAK2 mutation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is Essential Thrombocythemia?

A

Overproduction of megakaryocytes/ abnormal platelets

21
Q

What mutations are associated with Essential Thrombocythemia?

A

JAK2 or MPL

22
Q

What is Primary Myelofibrosis?

A

Fibrosis that obliterates the bone marrow and produces atypical megakaryocytes

23
Q

What is the genetic mutation associated with Primary Myelofibrosis?

A

JAK2 or MPL

24
Q

What is CML?

A

Overgrowth of granulocytic and megakaryocytic precursors in bone marrow due to BCR-ABL fusion gene

Can convert to AML

25
Q

What is myelodysplastic syndrome?

A

Class of stem cell disorders that result in ineffective hematopoiesis; causes defects in cell maturation of all non-lymphoid lineages

Can convert to AML

26
Q

What viral infection causes the predominance of B-cell Lymphoid malignancies?

A

EBV

27
Q

What cells is ALL typically derived from?

A

Immature B-cells

28
Q

In CLL and lymphoma, what is the malignant cell population?

A

Mature B-cells

29
Q

What is the difference between the locations of malignant cells in CLL and lymphoma?

A

CLL= blood

Lymphoma= lymph node or other tissues

30
Q

What cells are malignant in myeloma?

A

Plasma cells

31
Q

What do malignant plasma cells in myeloma produce?

A

Monoclonal immunoglobulin

32
Q

What is the difference between Hodgkin and Non-Hodgkin Lymphoma?

A

Presence of absence of Reed-Sternberg cell

33
Q

What are Reed-Sternberg cells, and what are the characteristics of Reed-Sternberg cells?

A

These are tumor giant cells seen in Hodgkin’s Disease. Characteristics include:

  • Large size
  • 2+ nuclei (bilobed) that give an “OWL EYE” appearance
  • Eosinophilic nucleolus
  • CD15 and CD30+
34
Q

Describe the progression of Hodgkin Lymphoma.

A
  • Hodgkin Lymphoma is localized to a single group of lymph nodes
  • Spread is contiguous and predictable
35
Q

What is the prognosis for Hodgkin Lymphoma?

A

60-90% cure rate with radiation and chemotherapy i.e. GOOD PROGNOSIS

36
Q

What are the three categories of Non-Hodgkin Lymphoma?

A

Indolent
Aggressive
V. aggressive

37
Q

What are the characteristics of CLL?

A
  • Increased small round lymphocytes
  • Smudge cells

Smudge cells are fragile cells that break on PBS–causing a smudge*

38
Q

What the major plasma cell disorders.

A
  • Multiple myeloma
  • Plasmacytoma
  • Primary Amyloidosis
  • MGUS
  • POEMS Syndrome
  • Waldenstrom Macroglobinemia
39
Q

What is Multiple Myeloma?

A

Mature B-cell (plasma cell) cancer

40
Q

What PBS features is characteristic of Multiple Myeloma?

A

Rouleaux formation, which is RBCs stacked like poker chips on PBS

41
Q

What lab features are characteristic of Multiple Myeloma?

A

Increased immunoglobulin (IgG or IgA) in serum or urine

42
Q

What is a Solitary Plasmacytoma? What lab feature is characteristic of this disease?

A

This is a plasma cell tumor characterized by a single plasma cell tumor in the bone marrow.

  • NO or low immunoglobulin in the blood
43
Q

What is Primary Amyloidosis?

A

Plasma cells secrete monoclonal light chains

  • These are misfolded and form fibril deposits in tissue
  • Disrupts organ function
44
Q

What is MGUS?

A

“Monoclonal Gammopathy of Undetermined Significance”

  • This is the ASYMPTOMATIC PRECURSOR of mutiple myeloma see with production of immunoglobulin detected in serum or urine

**Only 1-2% of patients with MGUS progress to Multiple Myeloma per year; hence the “undetermined significance”

45
Q

What lab value is associated with Waldenstrom Macroglobulinemia?

A

IgM

Associated with hyperviscosity syndrome*

46
Q

How is Leukemia diagnosed?

A

PBS

Bone marrow biopsy

47
Q

What is lymphoma diagnosed?

A

Lymph node biopsy

48
Q

How are plasma cell neoplasms diagnosed?

A

Bone marrow biopsy