Lymphoma/ Leukemias Flashcards

1
Q

What illness has

Low Hemoglobin (Hb) and platelets

High WBC count

auer rods

MPO+

A

AML

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2
Q

Patients with infectious _____ have flu-like symptoms, lymphadenopathy, and splenomegaly.

Atypical Lymphoblasts on smear

(weird shaped)

A

mononucleosis

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3
Q

Mucosal Pallor =

A

Anemia

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4
Q

This patient’s combination of pancytopenia, hypercoagulability (eg, hepatic vein thrombosis), and anemia are characteristic of

A

paroxysmal nocturnal hemoglobinuria (PNH).

Pancytopenia

N-emia

Hypercoagulability

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5
Q

PNH is caused by an acquired mutation of the ___ gene within a clonal population of multipotent hematopoietic stem cells.

This gene is involved in the synthesis of the _______ anchor, a glycolipid necessary for the attachment of several cell-surface proteins, including _____ (decay-accelerating factor) and _____ (MAC inhibitory protein). These proteins help inactivate complement and prevent the membrane attack complex from forming on normal cells.

COOMBS Negative Hemolysis

A

PIG-A

glycosylphosphatidylinositol (GPI)

CD55

CD59

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6
Q

Patients with ______ mutation are at increased risk of thrombotic events

A

factor V Leiden

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7
Q

Easy bruising =

A

impaired platelet plug formation

vWF deficiency

Hemophilia

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8
Q

Head and neck squamous cell carcinomas typically spread first to the ____ lymph nodes via the lymphatics.

A

anterior cervical

The involvement of anterior cervical lymph nodes affects the staging of the disease.

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9
Q

____ reactions are usually mild, hemolytic reactions that occur >24 hours after blood transfusion (recent hospital visit).

Occurs in patients previously exposed to a minor RBC antigen (eg, previous blood transfusion, pregnancy).

(+ Coombs)

(+/– ↑ indirect bilirubin or ↑ lactate dehydrogenase)

A

Delayed hemolytic transfusion

They are a type of anamnestic response (delayed immunologic response

Additional laboratory findings include anemia with compensatory reticulocytosis and evidence of hemolysis

(+/– ↑ indirect bilirubin, ↑ lactate dehydrogenase).

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10
Q

____ reactions occur within minutes of transfusion initiation and present with wheezing, angioedema, and hypotension, findings not seen in this patient.

This reaction can occur in patients with IgA deficiency due to the reaction of recipient anti-IgA antibodies against donor IgA.

A

Anaphylactic transfusion

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11
Q

Rifampin, phenobarbital, and phenytoin are potent enhancers of the cytochrome P-450 pathway; concurrent use of warfarin with these medications results in _______ efficacy of warfarin.

A

decreased efficacy

(Low INR)

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12
Q

The presence of rod-shaped intracytoplasmic inclusions known as Auer rods is characteristic of many forms of acute myeloblastic leukemia (AML). The ___ variant of AML, acute promyelocytic leukemia, is associated with the cytogenetic abnormality t(__;__).

A

M3

t(15;17)

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13
Q

Deletion of ____ is one of the molecular defects seen in chronic lymphocytic leukemia.

A

13q

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14
Q

Mantle cell lymphoma is a B-cell malignancy associated with

t(__;__)

This translocation results in activation of the _____ gene.

A

t(11;14)

cyclin D

(Clock on the Mantle 11:14)

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15
Q

With t(__;__), associated with Burkitt lymphoma, t

A

t(8;14)

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16
Q

In Burkitt’s Lymphoma there is a translocation between the ___ protooncogene on chromosome 8 and the _____ region on chromosome 14. This leads to increased production of the oncogene due to the frequency with which the Ig gene is transcribed.

A

cMyc

Ig heavy chain

17
Q

Translocation of the ABL gene from chromosome 9 to chromosome 22 is characteristic of _______. t(9;22) forms the “Philadelphia chromosome” and results in the formation of a new gene, BCR-ABL, whose product has constitutively active ______.

A

chronic myelogenous leukemia

tyrosine kinase activity

18
Q

t(9,22) is associated with

A

CML

19
Q

t(15,17) cytogenetic change represents a translocation between the _____ gene on chromosome 17 and the _______ gene on chromosome 15.

Fusion of these 2 genes produces a chimeric gene product, ____ which codes for an abnormal ____ receptor.

This abnormal fusion gene inhibits promyelocyte differentiation and triggers the development of APML.

Management is with ______.

A

retinoic acid receptor alpha (RARα)

promyelocytic leukemia (PML)

PML/RARα

retinoic acid

all-trans retinoic acid

20
Q

Associated with CD15 and CD30 markers

A

Hodgkins Lymphoma

21
Q

Associated with EBV

or Jaw Lesion

A

burkitt’s Lymphoma

Non-Hodkins

22
Q

Associated with waxing/waning Lympoadenopathy

A

(indolent) Follicular lymphoma

23
Q

Associated with t(11;14)

A

Mantle Cell Lymphoma

24
Q

Associated with t(11;18)

A

Marginal Zone lymphoma

25
Q

Associated with Sjrogrens

Chronic Inflammatory illnesses

A

Marginal Zone Lymphoma

26
Q

Associated with HIV/AIDS or EBV

AIDS defining illness

Ring Enhancing Lesion

A

Primary CNS lymphoma

27
Q

Associated with HTLV or IVDU

A

Adult T-cell lymphoma

28
Q

Associated with skin patches/ plaques

cerebrifrom nuclei

pautrier microabscess (tumor cell aggregates in skin)

A

Mycosis Fungosis

Sezary

29
Q

B Cell Leukemias (2)

A

CLL (B)

Hairy Cell (B)

30
Q

T cell Leukemias (1)

Granulocyte Leukemias (2)

A

ALL (T)

AML, CML (Granulocytes)

31
Q

NHL Neoplasms of Mature B cells (6)

A

Burkitt

Diffuse Large B cell

Follicular

Mantle

Marginal Zone

Primary CNA lymphoma

32
Q

NHL Neoplasms of Mature T cells (2)

A

Adult T cell (tokyo) Lymphoma

Sezary Syndrome (M. Fungioides)

33
Q

Most common Hodkin Lymphoma

Women > Men

A

Nodular Sclerosis

34
Q

Hodkins lymphoma

Eosinophilia

Immunocompromised

A

Mixed Cellularity

35
Q

Hodkins Lymphoma

Seen in immunocompromised

NO eosionphils

A

Lymphocyte depleted

36
Q

Hodkins lymphoma with best prognosis

A

Lymphocyte rich