Heme/Onc Questions + Formatives Review Flashcards

1
Q

Immune Deficiency Linked to Increased Lymphomas

A

Wiskott Aldrich (T-Cell) - X-Linked

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2
Q

Teenage Mass with CD2 and CD7

A

Lymphoblastic Lymphoma - T-Cell + Teenager + Thymus

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3
Q

Follicular Lymphoma - Sample Markers (2) + Translocation

A

CD5 -
CD10 +
t:18:14 - Bcl2

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4
Q

CLL - Markers (3) + Smear vs. ALL

A

Markers - CD5+ / CD19+ / CD20+

Smear = Smaller more mature cells - Also usually smudge cells

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5
Q

Russell Bodies - 2 Disease + Key Difference

A

Russell Bodies - Multiple Myeloma + Waldenstrom-Macroglobulinemia (Lymphoblastic Lymphoma)

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6
Q

Anaplastic Large Cell Lymphoma (4)

A

ALK
2,5 Trans-location
Horseshoe Shaped Cells
CD-30

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7
Q

Drugs interacting with Methotraxate (4)

A

1) Aspirin
2) NSAIDS
3) Penicillins
4) Cephalosporins

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8
Q

HER2 Breast Cancer Drugs (3)

A

1) Tratsuzumab
2) Lapatinib
3) Peruzumab

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9
Q

Drug Correlated with Rash Efficacy (1) - 3 Keys

A

Erlotinib - EGFR Tyrosine Kinase Inhibitor

Used for Non-Small Cell Lung Cancer
CYP3A4

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10
Q

HPV - Carcinogenesis Pathway

A

Blocks Rb protein - No Rb protein = no inhibition of Cyclin D1 - Easy progression from G1-S

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11
Q

Von Hipple Lindaue - Genetics + Mechanism

A

1) Autosomal Dominant

2) Loss of VHL allows stabilization of HIF = Allows tumor angiogenesis

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12
Q

ATRA Syndrome - Cause + Findings (4)

A

ARTA - Used for 15/17 translocation in AML-M3

Cytokine storm - Causes hypotension + pleural effusions + respiratory distress + can be deadly

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13
Q

5-FU - Key Deficiency

A

Dihydropyrimidine dehydrogenase

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14
Q

Pneumocystis Carini - Key Immune Deficiency

A

Hyper IgM - Defective CD40 - X-Linked Recessive

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15
Q

AML - Poor Prognosis Markers (4)

A

1) 9:22 + 9:11 + Loss of Chromosomes

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16
Q

LAD-1 - Inheritance + Missing Marker + Triad

A

Autosomal Recessive

Missing CD18

Delayed Separation of the Umbilical Cord

17
Q

Job’s Syndrome - 4 Keys

A

1) Hyper IgE Syndrome (B-Cell) - Eosinophilia
2) Triad - Eosinophilia + Eczema + Recurrent Sinopulmonary Infactions
3) Autosomal Dominant
4) JAK/STAT3 Over-activation

18
Q

Myeloperoxidase Deficiency - 3 Keys

A

Loss of Conversion of H2O2 to HOCl

Increased Candida Infection

Normal Nitro Blue Test

19
Q

LAP Stain - Uses (2)

A
LAP+ = Leukemoid Reaction (Acute Infection
LAP- = CML

CML = Basophils vs. Acute Leukemoid = Neturophils

CML - Lots of granulocytes (lots of lobs)

20
Q

CML Keys

A

1) Classicly presents just with elevated WBC/Hb/Platelet and Enlarged Spleen
2) t(9:22) BCR-Abl - RIsk of AML/ALL Progression
3) Treatment = Busulfan

21
Q

Heriditary Spherocytosis - Key Points (3)

A

1) Red Spherocytes - Normocytic + Extravascular
2) Autosomal Dominant
3) Spectin/Anykin
4) Osmotic Fragility Test

22
Q

Major Tests for Heme/Onc (8)

A

1) Nitro Blue - Chronic Granulomatous Disease
2) D-Dimer - DIC
3) Schilling Test - B12
4) Metabisulfite Test - HbS - Trait/Disease
5) Osmotic Fragility - Heriditary Spherocytosis
6) Sucrose Test - PNH + CD55 Follow-Up
7) Ristocetin Test - Benard Soulier + vWF Disease
8) Mixing Test - Lack of a Factor vs. Ab against a Factor

23
Q

3 Transfusion Issues Prevented by Leukodelpletion

A

1) TRALI
2) Febrile Reaction
3) CMV infection

24
Q

TRALI - Keys (4)

A

1) 1-2 Hours After Transfusion
2) Severe Hypotension + Pulmonary Edema

3) Antibodies against donor HLA - Antibodies cause massive immune reaction with endothelial damage and fluid leak (pulm. edema)
4) #1 Cause of Transfusion Death

25
Q

Mantle Cell Lymphoma - CD Marker + Translocation

A

CD5 Positive

t:11/14 - Cyclin D1

26
Q

Horseshoe Shaped Nuclei

A

ALK - T-Cell + CD30 + 2,5 Trans

27
Q

Cloverleaf Cells - Disease + Findings (2)

A

A-TALL - Aggressive + HLTV-1 Infection

28
Q

Diseases with Large Platelets

A

1) ET
2) ITP
3) Bernard Soiler

29
Q

High Uric Acid - Class of Diseases

A

Myeloproliferative

30
Q

Darocytes

A

Tear Drop Cell - Myelofibrosis - Fibrosis of bone marrow with intravascualr hemolysis and atypical megakarocytes - extramedullay hematopoesis