Hematology Flashcards

1
Q

How does anemia kill?

A

Myocardial ischemia

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2
Q

Additional tests for anemia include

A
retic count
haptoglobin
LDH
total/direct bilirubin]
TSH and T4
B12/folate levels
iron studies

also order urinalysis with microscopic analysis

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3
Q

Anemia of chronic disease shows what on Iron studies?

A

High/Normal ferritin
Low total iron binding content (TIBC)
Low iron
Normal or low Fe sat

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4
Q

Iron deficiency anemia shows what on Iron studies?

A
Low ferritin
High TIBC
Low Iron
Low Fe sat
ELEVATED RDW!!!
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5
Q

Elevated RDW? Think

A

iron deficiency

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6
Q

Iron levels will be high in

A

Alcoholic
Isoniazid
Lead exposure

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7
Q

Unexplained microcytic anemia in patient >50 is probably

A

Colon cancer

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8
Q

The only Anemia of chronic disease that responds to EPO is that caused by

A

end stage renal disease

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9
Q

What drug blocks B12 absorption?

A

Metformin! Fun fact!

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10
Q

Drugs that block GI absorption of folate are

A

alcohol
nitrofurantoin
estrogens
phenytoin

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11
Q

In B12 deficiency, the reticulocyte count is __ because of ineffective erythropoiesis

A

LOW; B12 deficiency destroys red cells early as they come out of the bone marrow

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12
Q

___ levels go up in both B12 and folate deficiency, but __ levels only go up in B12 deficiency

A

Homocysteine; methylmalonic acid

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13
Q

To discover the cause of B12 deficiency, check __ and __ levels

A

antiparietal cell antibodies and anti intrinsic factor antibodies!

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14
Q

What are four tests indicative of hemolysis?

A
LDH
Indirect bilirubin
Haptoglobin
Reticulocyte level
Also order a peripheral smear!
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15
Q

Watch for low __ after treating B12 deficiency!

A

Potassium

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16
Q

Fever in a patient with Sickle Cell Disease is an emergency because

A

the patient has no spleen!

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17
Q

If a fever is present in SCD patient, give

A

ceftriaxone

levofloxacin or moxifloxacin

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18
Q

When is the answer exchange transfusion for SCD?

A

Retinal infarction
pulmonary infarction leading to pleuritic pain and abnml xray
priapism
stroke

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19
Q

The only findings of sickle cell trait are

A

Renal manifestations (hematuria)

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20
Q

Syphilis causes __ with IVIG

A

cold agglutinins

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21
Q

Heinz bodies and bite cells can appear in patients with

A

G6PD Deficiency

22
Q

__ deficiency presents the same way as G6PD deficiency except it’s unclear what provokes the hemolysis

A

Pyruvate kinase deficiency

23
Q

The most accurate test for hereditary spherocytosis is

A

eosin-5-maleimide

24
Q

The treatment for hereditary spherocytosis is

A

splenectomy

25
Genetic loss of ankyrin and spectrin =
hereditary spherocytosis
26
Autoimmune hemolysis + Renal failure + Thrombocytopenia =
Hemolytic Uremic Syndrome
27
TTP is HUS +
fever + neurologic issues
28
What level is down in TTP?
ADAMTS-13
29
Do NOT give ___ in HUS or TTP!
platelets!
30
The purpose of plasmapheresis in the treatment of severe TTP is to
replace ADAMTS-13, a metalloproteinase that breaks down VWF
31
Treat severe paroxysmal nocturnal hemoglobinuria with
Eculizumab, an inhibitor of C-5 that prevents complement activation Treat mild dz with steroids
32
PNH can transform into
aplastic anemia | Acute myelogenous leukemia
33
HELLP syndrome stands for
hemolysis elevated liver function tests low platelets Deliver that baybay
34
Shortness of breath, clear lungs, brown blood =
methemoglobinemia treat with methylene blue
35
M3 acute promyelocytic leukemia is associated with
DIC
36
Treat M3 APL with
all trans retinoic acid
37
A special neutrophil in myelodysplasia with 2 lobes is called a
Pelger-Huet cell
38
The most common cause of death in myelodysplasia is
infection or bleeding
39
Best treatment for CML is
imatinib initially | Bone marrow transplant is the only cure but not initial
40
Smudge cells =
CLL
41
Best initial therapy for hairy cell leukemia is
cladribine (2-CDA)
42
Both hairy cell leukemia and myelofibrosis present with __ and __
pancytopenia and splenomegaly
43
EPO level is ___ in polycythemia vera
low
44
JAK2 mutation is found in__, __, and __
Myelofibrosis, polycythemia vera, and essential thrombocythemia
45
Daily aspirin should be given to patients with
polycythemia vera and essential thrombocythemia
46
The key feature of essential thrombocythemia is
markedly elevated PLATELET count | -Treat with hydroxyurea to lower the platelet count
47
The most frequent presentation of ___ is bone pain caused by fracture occurring under normal use
multiple myeloma
48
Treat multiple myeloma with
melphalan and steroids | Thalidomide, lenalidomide, or bortezomib may be added
49
The most effective therapy for multiple myeloma is
autologous stem cell bone marrow transplantation
50
Elevated protein level found in an elderly person =
monoclonal gammopathy of unknown significance
51
HIT is an ___ reaction characterized by a drop in platelets a few days AFTER the start of heparin
allergic
52
___ is safe in HIT
Fondaparinux