HEME AND ONC Flashcards

1
Q

hat are the macrocytic anemias? What would we see on a blood smear with these anemias?

A

B12 and Folate deficiency

Megaloblastic (hypersegmented neutrophils)

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2
Q

What would a pt have with B12 deficiency?

A

Peripheral neuropathy

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3
Q

What type of anemia may be secondary to alcoholism?

A

Folate deficiency

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4
Q

What type of anemia is associated with glossitis?

A

Folate (can also occur in B12)

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5
Q

What are the microcytic anemias? What consititues as microcytic?

A
*TICS*
              Anemia or chronic disease
              Iron def anemia
              Thalassemia
              Sideroblastic
              MCV is less than 80
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6
Q

What are the differences between Anemia of chronic dz and iron def anemia?

A

Both have LOW Serum Iron
Ferritin is NORMAL in ACD
Ferritin is LOW in IDA
IDA will also have a high iron binding capacity

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7
Q

What is the max amount of ferrous sulfate a person absorb/day?

A

Max = 4mg

Males require 1mg

Females require 2mg (more if preggo)

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8
Q

If the iron levels are normal but the MCV is still less than 80, what should you think of?

A

Thalassemia or sideroblastic

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9
Q

What is thalassemia?

A

Reduced or absent beta or alpha chain

*Normal hemoglobin is made up of two alpha globin & two beta globin chains

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10
Q

How do you diagnose a thalassemia?

A

Electrophoresis (Hgb A2 and F)

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11
Q

When would we see Beta thalassemia diagnosed?

A

Intermediate and Major occur between 4-6months when the switch from fetal hemoglobin to adult occurs

Minor is asymptomatic

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12
Q

How do we treat alpha vs beta thalassemia?

A

Alpha H – folic acid supplements, avoid iron supplements

Beta = transfusions, iron chelation

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13
Q

What is the MC cause of sideroblastic anemia? Dx?

A

Lead toxicity

Lead level followed by bone marrow biopsy

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14
Q

What would normocytic anemia be caused from? What are the MCV levels?

A

Acute blood loss, organ failure, or impaired marrow function.

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15
Q

What is hemolytic anemia?

A

HIT (hereditary, immune attack, and trauma to the RBCs); characterized by decreased RBC survival and increased cell lysis

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16
Q

What are some of the causes of hemolytic anemias?

A

spherocytosis, elliptocytosis, G6PD, thalassemias, and sickle cell

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17
Q

How might a patient present with hemolytic anemia?

A

Jaundice, delayed puberty (from sickle cell), hepatosplenomegaly, and petechiae and purapura

18
Q

Target cells are associated with what?

A

Thalassemias

19
Q

Heinz body or bite cells are associated with what?

20
Q

Howell-Jolly cells are associated with what?

A

Folate def (can also be seen in a Sickle cell smear)

21
Q

A pt presents with epistaxis, HA, dizzy. The pt notes extreme pururitis last night after bathing – dx?

A

Polycythemia vera

22
Q

What would be seen on labs with polycythemia vera?

A

Increased number of RBC’s and increased total blood volume

Thrombocytosis, leukocytosis, increased basophils and eosinophils, and increased number of large platelets

23
Q

How do we treat polycythemia vera?

A

Phlebotomy and low-dose aspirin

24
Q

What is the classification system for leukemias?

A

Acute or Chronic

Myelocytic or Lymphocytic

25
What type of leukemia MC occurs in young children?
ALL
26
What type of leukemia typically occurs in adults over the age of 60?
AML
27
What type of leukemia presents in young to middle aged adults?
CML
28
What type of leukemia has the worst prognosis?
CLL
29
Auer rods are associated with what type of leukemia?
AML
30
The Philadelphia chromosome is associated with what?
CML
31
Smudge cells are associated with what?
CLL
32
What is the standard of treatment for acute leukemias?
Chemotherapy *better prognosis in AML if under the age of 60
33
How do we treat CML? CLL?
Imatinib and allogeneic bone marrow transplantation CLL is palliative care
34
Reed-Sternberg cells are associated with what?
Hodgkin disease (along with enlarged spleen and liver)
35
What type of hodgkin’s is found in patients aged 15-45?
Hodgkin’s disease
36
How do we treat Hodgkin’s?
chemo and radiation
37
Which type of hodgkin’s has a better prognosis?
Hodgkin’s
38
A pt presents with bone pain and anemia – what dx? Workup?
Multiple myeloma Monoclonic spike on serum protein electrophoresis *Bence-Jones protein in urine Lytic lesions on xray
39
What is considered mild thrombocytopenia?
100,00 – 150,000 platelets
40
What is considered severe thrombocytopenia?
less than 50,000 platelets
41
When/how to we start treatment for thrombocytopenia?
start when platelets are less than 30,000 Start with glucocorticoids (+/- IVIG) Splenectomy