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
Q

Genetic loss of ankyrin and spectrin =

A

hereditary spherocytosis

26
Q

Autoimmune hemolysis + Renal failure + Thrombocytopenia =

A

Hemolytic Uremic Syndrome

27
Q

TTP is HUS +

A

fever + neurologic issues

28
Q

What level is down in TTP?

A

ADAMTS-13

29
Q

Do NOT give ___ in HUS or TTP!

A

platelets!

30
Q

The purpose of plasmapheresis in the treatment of severe TTP is to

A

replace ADAMTS-13, a metalloproteinase that breaks down VWF

31
Q

Treat severe paroxysmal nocturnal hemoglobinuria with

A

Eculizumab, an inhibitor of C-5 that prevents complement activation

Treat mild dz with steroids

32
Q

PNH can transform into

A

aplastic anemia

Acute myelogenous leukemia

33
Q

HELLP syndrome stands for

A

hemolysis
elevated liver function tests
low platelets

Deliver that baybay

34
Q

Shortness of breath, clear lungs, brown blood =

A

methemoglobinemia

treat with methylene blue

35
Q

M3 acute promyelocytic leukemia is associated with

A

DIC

36
Q

Treat M3 APL with

A

all trans retinoic acid

37
Q

A special neutrophil in myelodysplasia with 2 lobes is called a

A

Pelger-Huet cell

38
Q

The most common cause of death in myelodysplasia is

A

infection or bleeding

39
Q

Best treatment for CML is

A

imatinib initially

Bone marrow transplant is the only cure but not initial

40
Q

Smudge cells =

A

CLL

41
Q

Best initial therapy for hairy cell leukemia is

A

cladribine (2-CDA)

42
Q

Both hairy cell leukemia and myelofibrosis present with __ and __

A

pancytopenia and splenomegaly

43
Q

EPO level is ___ in polycythemia vera

A

low

44
Q

JAK2 mutation is found in__, __, and __

A

Myelofibrosis, polycythemia vera, and essential thrombocythemia

45
Q

Daily aspirin should be given to patients with

A

polycythemia vera and essential thrombocythemia

46
Q

The key feature of essential thrombocythemia is

A

markedly elevated PLATELET count

-Treat with hydroxyurea to lower the platelet count

47
Q

The most frequent presentation of ___ is bone pain caused by fracture occurring under normal use

A

multiple myeloma

48
Q

Treat multiple myeloma with

A

melphalan and steroids

Thalidomide, lenalidomide, or bortezomib may be added

49
Q

The most effective therapy for multiple myeloma is

A

autologous stem cell bone marrow transplantation

50
Q

Elevated protein level found in an elderly person =

A

monoclonal gammopathy of unknown significance

51
Q

HIT is an ___ reaction characterized by a drop in platelets a few days AFTER the start of heparin

A

allergic

52
Q

___ is safe in HIT

A

Fondaparinux