Hematology/ Oncology Flashcards

(49 cards)

1
Q

Macrocytic Anemia MCV

A

> 100

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2
Q

Causes of nonmegaloblastic Anemia

A

Liver disease
EtOH
Drugs
Metabolic

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3
Q

Causes of Megaloblastic Anemia

A

B12 or Folate deficiency

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4
Q

Drugs that cause a nonmegaloblastic anemia

A

5FU
Ara-C
AZT, Zidovudine

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5
Q

Causes of Microcytic Anemia

A

Thalassemia
Iron Deficiency
Chronic Inflammation
IDA

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6
Q

Thalassemia Hx, Dx, Tx

A
Anemia 
Dx: Iron studies normal 
Hgb Electropheresis 
find any other hemoglobin other than normal = beta thalassemia 
Tx: beta-transfusion 
for iron overload use defuroxamine
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7
Q

Normocytic anemia Dx

A

LDH elevated
Bilirubin Elevated
Haptoglobin Decreased
Means hemolysis

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8
Q

G6PD deficiency Hx, Dx

A

African American male taking Dapsone, TMP-SMX, Nitrofurantoin
Dx-Heinz bodies, Bite cells
Tx: Supportive
Avoid Stress

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9
Q

Sickle Cell Vasoocclusive Crises Dx and Tx

A
Acute chest-MI
Brain CVA- Exchange transfusion 
Priapism 
Dx: Hgb electrophoresis 
Smear- Sickled Cells 
Long term treatment hydroxyurea 
Acute- IVF, pain meds, O2
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10
Q

AHI Coombs test

A

IgM-cold type caused by mycoplasma and mono
IgG warm Type-AI, CA,
use steroids, rituximab, splenectomy

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11
Q

AML M3 Variant Treatment

A

All Transretnoic Acid

presence of Auer Rods

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12
Q

CML bone marrow biopsy finding

A

Philadelphia Chromosome t(9,22) BCR-ABL

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13
Q

Non-tender lymphadenopathy indicates?

A

Cancer

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14
Q

Hodgkins with B symptoms presentation

A

Night Sweats
Fever
Weight loss
LN pain with ingestion of alcohol

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15
Q

Hodgkins Tx

A

ABVD or BEACOPP

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16
Q

Non-Hodgkins Tx

A

Rituximab or R-CHOP

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17
Q

Reed Sternberg cells found in what disease and what are the markers

A

CD 15 , CD 30

Hodgkins

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18
Q

Adriamycin, Doxirubicin AE

A

Cardiotoxicity

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19
Q

Vincristine/Vinblastine

A

Peripheral Neuropathy

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20
Q

Bleomycin AE

A

Pulm Fibrosis

21
Q

Cisplatin AE

A

Ototoxicity

Nephrotoxicity

22
Q

Cyclophosphamide AE

A

Hemorrhagic cystitis

23
Q

which is worse hodgkins or non-hodgkins

24
Q

Plasma cell disorder presentation (Multiple Myeloma) CRAB

A

Hypercalcemia
Renal Failure
Anemia
Bone Pain

25
Multiple Myeloma Dx
Spep=M spike Upep=M-Spike Skeletal changes BMBx->10% Plasma
26
Multiple Myeloma Tx
>70, no donor=chemo | <70, donor-Stem cell transplant
27
MGUS Hx, Dx, Tx
Asx Dx- online Spep Positive BMBx <10% Plasma cells Tx: Monitor and observe
28
Waldenstroms Hx, Dx, Tx
``` Hyperviscosity with constitutional symptoms Dx: Spep positive Upep and skeletal negative BMBx- >10% plasma Tx: Rituximab Plasampheresis ```
29
TTP presentation | FATRN
``` Fever Anemia (microangiopathic) Thrombocytopenia Renal Failure Neuro Sxs ```
30
TTP Dx
Decreased platelets PT/PTT normal Fibrinogen Normal D-Dimer Normal
31
TTP Tx
Exchange transfusion
32
DIC Dx
Platelets decreased PT/PTT increased D-Dimer Increased Fibrinogen Decreased
33
``` Elevated T. bili LDH Decreased Haptoglobin ```
Hemolysis | perform Smear
34
Folate Deficiency Presentation
Pt: Tea and Toast Diet Dx: Folate level MMA normal Tx: Folic Acid
35
B12 Deficiency Presentation
``` Pt: Neuro Sxs Strict vegan Dx: Decreased B12 increased MMA Schillings Test Tx: PO- nutritional deficiency IM B12- Impaired Absorption ```
36
Schillings test
Give IM B12 then oral B12 if Urine (+) B12-nutritional def Urine (-) B12- Absorption
37
Iron Deficiency Anemia Presentation
``` Pt: Slow bleeds Old Male (+) Fecal Occult Blood Test Woman W/ Mennorrhagia Dx: Decreased Fe, Ferritin Increased TIBC Tx: replace, 324mg Iron Stool Softeners ```
38
Anemia of Chronic Disease Presentation
``` Pt: Chronic Inflammatory Disease (SLE, RA) Usually Asx Hgb >8 Dx: Increased Ferritin Decreased TIBC, Fe Tx: Usually nothing maybe EPO ```
39
Heriditary Spherocytosis Presentation
``` (Spectrin, ankryin, Pallidin) Pt: Hemolysis Smear shows Spherocytes Dx: Smear Osmotic Fragility Test Tx: Splenectomy ```
40
Paroxysmal Nocturnal Hemolglobinuria Presentation
Deficiency PIGA gene Dx: Flow cytometry showing deficiency CD 55 Tx: Supportive Ecluzimab
41
AML presentation
``` Pt: Acute 67 y.o. Exposure- Benzine, Radiation CML: Blast crisis transformation Dx: Smear Bone marrow Bx->20% blasts + Myeloperoxidase non-M3 Variant-Chemo ```
42
CML presentation
Pt: Asx with increase white count Dx: Bone marrow Bx- Philadelphia Chromosome t(9.22) BCR-ABL Tx: Imatinib can transform into AML (Blast Crisis)
43
ALL presentation
``` Pt: Acute, Young Patient Dx: Smear BMBx >20% blasts (Positive Tdt) Tx: Chemo ppx CNS with ARA-C ```
44
CLL Presentation
``` Pt: Chronic Older Patient Dx: Diff BMBx Tx: >65 +Asx= no treatment >65 + Sx = Chemo <65 +Donor = Stem Cell Transplant ```
45
Von Willebrand Disease Presentation
``` Decreased vWF and Factor 8 Pt: Platelet bleeding (superficial-Gums, vagina, petechiae) Normal platelet count Dx: vWF Tx: DDVAP Factor 8 ```
46
DIC Presentation
Very sick patient Sepsis, ICU Shock
47
Heparin Induced Thrombocytopenia Tx
Stop heparin Start Argatoban Bridge to Warfarin
48
HIT Presentation
Presents 7-14 days after starting
49
Idiopathi Thrombocytopenic Purpura Presentation, Tx
``` Usually a Female with AI Diagnosis of exclusion Tx: Steroids-Acute Critically Low- IVIg Splenectomy-Refractory Rescue therapy-Rituximab ```