heme Flashcards

1
Q

what substances are known for causing hemolytic anemia in G6Pd def

“Spleen purges nasty inclusiong from damaged cells”

A

Sulfonamides

Primaquine

Nitrofrantoin

Isoniazid

Fava beans

Dapsone

Chloroquine (antimalarial)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

whats the life span of a platelet (including after transfusion)

A

8-10 days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what molecule is expressed on the surface of a platelet after the platelet is activated by binding of ADP to P2Y12?

A

Gpllb/llla

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

most common inherited coagulation (bleeding) disorder?

A

von Willebrand disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

tx and diagnostic findings for

von willebrand disease

A

(DDAVP) Desmopressin

PT-, BT inc, .PT - , PTT -/ inc

use Ristocetin cofactor assay

if no VWF then no platelet aggregation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what platelet disorder

Anti-gpllb/llla antibodies

A

ITP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what platelet disorder

ADAMTS -13 def

A

TTP

(DIT says alos HUS)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what platelet disorder

gp lb defect

A

bernard-soulier syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what platelet disorder

gpllb/llla defect

A

Glanzmann’s thrombasthenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what platelet disorder

VWF defect

A

von willbrand disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what platelet disorder

wide spread activation of platelets and coagulation cascade

A

DIC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what platelet diseases are chronic

A

genetic:

  • VWD (Autosomal dom)
  • Bernard soulier syndrome
  • glanzmanns thrombasthenia

non-genetic: anti-gpllb/llla

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

mc leukemia in children

A

ALL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

mc leukemia in adults in the us

A

CLL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

chracteristic Auer rods

A

AML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

MYELODYSPLASTIC syndromes have a tendency to progress to?

17
Q

more than 20% blasts in the marrow indicates?

A

acute leukemia

18
Q

leukemia with more mature cells and < 5% blasts

A

chronic leukemia

19
Q

TdT (+) acute leukemia

20
Q

COMMONLY presents with BONE pain

21
Q

numerous basophils, splenomegaly

and negative for leukocyte alkaline phospahtes* (LAP)

22
Q

always positive for the

Philadelphia chromosome t(9,22)

23
Q

Acute leukemia postive for peroxidase (myeloperoxidase)

24
Q

solid sheets of lymphoblasts in marrow

25
always associated with the ***BCR-ABL*** gene
**CML**
26
**SMUDGE cells**
**CLL**
27
Reddish-pink rods in the Cytoplasm of leukemic blasts
Auer rods (AML)
28
what disease is associated with these findings ## Footnote **punched out lytic bone lesions**
**multiple myeloma**
29
what disease is associated with these findings RBCs clumped together like a stack of coins
Multiple myeloma
30
what disease is associated with these findings ## Footnote **plethora + Pruritus + Headache**
**polycythemia vera**
31
**HYPERcalcemia** **back pain** **anemia** **renal insufficiency**
**Multiple myeloma**
32
what disease is associated with these findings ## Footnote **teardrop shaped RBCs**
**Myelofibrosis**
33
what disease is associated with these findings ## Footnote **monoclonal antibody spike**
**multiple myeloma** **MGUS** **Waldenstrom macroglobulinemia** (no "CRAB" symptoms)
34
pt is diagnosed with Multiple myeloma what will be seen on urinalysis (UA)?
**no proteinuria on routine urinalysis** must get UPEP to see monoclonal antibody spike..
35