L31/32:Hem Flashcards

1
Q

An older adult comes into clinic with bone pain, anemia, and elevated creatine. They state they have felt they keep getting sick lately. Which condition is this?

A

Multiple Myeloma

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2
Q

In plasma cell disorders, the monoclonal plasma cells produce monoclonal immunoglobulins that is identified on serum protein electrophoresis as a monoclonal spike, also known as…
A. IgG
B. M protein
C. IgM
D. IgA

A

B. M protein

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3
Q

Which test is used to identify the subtype of immunoglobulin and the light chain (kappa/lamda) present on the immunoglobulin responsible for the monoclonal spike seen on serum protein electrophoresis?

A

Serum immunofixation

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4
Q

True or False: Monoclonal immunoglobulins are found in serum of patients with multiple myeloma and Wldenstroms macroglobulinemia

A

True

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5
Q

Clonal bone marrow plasma cells ≥10% or biopsy-proven bony/
extramedullary plasmacytoma suggests a dx of…

A

multiple myeloma

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6
Q

Waldenstrom Macroglobulinemia is a malignancy of lymphoplasmacytoid cells that secrete ___

A

IgM

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7
Q

Unlike multiple myeloma, in Waldenstrom Macroglobulinemia, patients present with ____ and ____

A

lymphadenopathy and hepatosplenomegaly

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8
Q

True or False: There are no lytic lesions in Waldenstrom Macroglobulinemia

A

True

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9
Q

____: Bone marrow infiltration by IgM plasma cells and lytic bone lesions

A

IgM Myeloma

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10
Q

True or False: Hyperviscosity is a symptom of multiple myeloma

A

False - symptom ov Waldenstrom Macroglobulinemia

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11
Q

Monoclonal IgM on serum protein electrophoresis (SPEP) test, as well as Rouleaux formation in peripheral blood RBC suggests….

A

Waldenstrom Macroglobulinemia

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12
Q

_____: Clonal stem cell disorder that occurs in patients who have the Philadelphia chromosome (translocation between chromosome 9 and 22)

A

Chronic Myeloid Leukemia

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13
Q

True or False: Chronic Myeloid Leukemia results in abnormally low expression of tyrosine kinase gene and abnormal proliferation of granulocytes

A

False -
1) while yes, there is abnormal proliferation of granulocytes
2) there is tyrosine kinase that is “on”

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14
Q

A 55 y/o patient presents with fatigue, night sweats, sternal tenderness, and splenomegaly. Which condition do they have?
A. Waldenstrom Macroglobulinemia
B. Chronic Myeloid Leukemia
C. IgM Myeloma
D. Multiple Myeloma

A

B. Chronic Myeloid Leukemia

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15
Q

True or False: Leukocytosis with left shift + hypercellular bone marrow with left shift suggests Multiple Myeloma

A

False - suggests Chronic Myeloid Leukemia

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16
Q

Three stages of CML? Features?

A

1) Chronic Phase: Increased WBC - due to granulocyte proliferation
2) Accelerated: blast count 10-20%
3) Blast phase: Blast >20% in blood/bone marrow

17
Q

Treatment for CML?

A

Tyrosine kinase inhibitors

18
Q

_____: Elevated red cell mass in the absence of a secondary condition

A

Polycythemia Vera (PV)

19
Q

Mutation in auto-inhibitory, pseudokinase domain of tyrosine kinase JAK-2 is most closely associated with which condition…

A

PV (polycythemia vera)

20
Q

Expanded blood volume and hyperviscosity are clinical features of polycythemia vera. How does this manifest?

A

1) Headaches
2) Fatigue
3) Blurred vision

21
Q

True or False: General pruritus occurs in polycythemia vera, as well as hepatomegaly and engorged retinal veins

A

False - all true, except there’s splenomegaly (not hepato)

22
Q

Increased Hb and Hematocrit, decreased erythropoietin, as well as (+) JAK2 mutation suggests which condition….
A. MM
B. PV
C. Chronic Myeloid Leukemia

A

B. PV

23
Q

How do you decreased blood viscosity and improve oxygenation in PV patients?

A

Phlebotomy

24
Q

Which type of bone marrow transplantation is prone to graft vs. host disease vs. rejection?
A. Autologous
B. Syngeneic
C. Allogeneic

A

C. Allogeneic

25
Q

Indications for Bone marrow transplant?
BOM NAH

A

Breast CA
Ovarian CA
Myeloma

Non-Hod Lymp
Hod Lymph
AML

26
Q

Which of the following receives granulocyte colony stimulating factor?
A. Bone Donor
B. Bone Recipient

A

A. Bone Donor

27
Q

What are the two types of Acute Leukemias?

A

Acute Myeloid Leukemia (AML)

Acute Lymphoblastic Leukemia (ALL)

28
Q

____: A hematologic malignancy characterized by an increase in the number of myeloid cells in the marrow and ARREST in their maturation, frequently resulting in hematopoetic insufficiency WITH/WITHOUT leukocytosis

A

Acute Myeloid Leukemia (AML)

29
Q
A
30
Q

Pancytopenia with circulating blast cells is a hallmark of which condition?

A

AML

31
Q

Auer rods suggest bone marrow ___

A

AML

32
Q

_____: Surface marker molecules that are cell membrane proteins (glycoproteins) or receptors (antigens) – allows for identification of MULTIPLE cell lines

A

Cluster Differentiation antigens (CD)

33
Q

__ ___ helps to identify if blast cells are
myeloid or lymphoid or bi-phenotypic in acute
leukemia based on cluster differentiation
antigens

A

Flow cytometry

34
Q

True or False: APL (AML M3) is the most curable subtype of AML but DIC is a complication

A

True