Hematology Flashcards

(43 cards)

1
Q

ADAMTS13

A

It’s VWF cleaving enzyme and associated with TTP

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2
Q

TTP Symptoms

A
Fever
AKI
Neuro ( seizure , Stroke , delirium )
Low platelets
Hemolytic anemia
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3
Q

HUS

A
Fever ( diarrhea before due to E.coli )
AKI
Hemolytic anemia 
Low platelets 
NO NURO
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4
Q

TTP Vs HUS

A

HUS : diarrhea , No Neuro , AKI with higher creatinine

TTP : ADAMTS13 , With neuro , less AKI

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5
Q

Schistocytes seen in

A

DIC
TTP
HUS

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6
Q

Waldenstrom Macroglobulinemia

A

Disorder of the B-cell ( IgM )

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7
Q

Waldenstrom Macroglobulinemia presentation

A

Hyperviscosity ( High IgM )
Cryoglobulunemia ( Raynaud phenomenon )
Cold agglutinins disease

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8
Q

Waldenstrom Macroglobulinemia Dx

A

Bone marrow biopsy

Dutcher bodies +IgM

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9
Q

MUGS

A

Monoclonal gammopathy of undetermined significance
This is the precursor of two diseases
1. Multiple Myeloma ( IgG + IgA )
2. Walden storm macroglobulenemia

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10
Q

Amyloidosis Major sites of clinically important dispositions

A

Kidney
Heart
Liver

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11
Q

Amyloidosis DX

A

Tissue biopsy with Congo red staining.

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12
Q

Esophageal cancer

A

Barret - Adenocarcinoma

Plummer Vinson - Sqamous cell carcinoma

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13
Q

Prussian blue

A

It’s spider oblast is anemia

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14
Q

Bite cells + Hence bodies

A

G6PD

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15
Q

Coombs +

A

Autoimmune heamolysis

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16
Q

Reedstenberg

A

Hodgkin disease

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17
Q

High RDW

A

It’s only Iron deficiency Anemia

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18
Q

Aur rods

19
Q

Iron deficiency Anemia 2 only’s

A
  • High RDW.

- Low ferritin. ( ferritin t store t )

20
Q

hypersegmented neutrophils

A

Folate + B12 deficiency

21
Q

Target Cell

22
Q

All RBC production problems give you

A

Low retic count .. Either Folate + B12 or Thlasemia and iron def etc

No contents of the retic how we gonna make the retics

23
Q

The only Low MCV and High retic Count is

A

3 gene deletion

24
Q

Hypothyroidism Anemia is

A

Macrocytic Anemia
This Big MCV one
Also liver disease Macrocytic

25
Very Well known medication that cause Folate deficiency
Phenytoin
26
Reticulocytes
Larger Cells than RBs | They are retained placenta BIG ones
27
Very low Hematocrit | Very low Hgb
25-30 | 8-10
28
1 unit of Packed RBC
Raise the hematocrit (3 points) | Raise the Hgb ( 1 point )
29
Warfarin Overdose reversed by
PCC Prothrombin complex concentrate 2 7 9 10 NOT FFP
30
Tx. Hemophilia A&B VWD
Factor 8 or 9 / Desmopressin DDVAP | Factor 8 or / Desmopressin DDVAP
31
NOAC Overdose
Idarusizumab
32
FFP Replaces
Clotting Factors | It’s need blood type
33
Hepcidin
Keep in the iron Trapped in the Store so you can’t use it
34
Anisocytosis
Unequal RBC sizes
35
HIT
IgG AB Against PF4 4-10 days after heparin More than 50% drop in platelets count TX is stop heparin + foundaparinux / argatroban / lipirudin Complications: Arterial and venous thrombosis
36
Wells score
Risk assessment for DVT
37
Thalassemia minor labs
RBC count normal Hgb normal RDW normal EXCEPT Low MCV
38
Only thing change in the lab of thalassemia minors patient is
Low MCV .. It’s microcytic anemia
39
Thalassemia Chromosomes A thalassemia B thalassemia
Chr.16 | Chr.11
40
Most Accurate test for Thalasemia diagnosis
Genetic testing It’s autosomal recessive disease so A thalassemia Chr.16 B thalassemia Chr.11
41
Normal Adult Hemoglobin component
A :97% A2 : 2 % F: 1%
42
Disorder in the heme part of the Hgb is two
Heme - Iron def / Chronic disease | Protoporphyrin- Sideroblastic
43
Tumor lysis syndrome
Associated with hematologic malignancies After initiation of cytotoxic Chemotherapy 1. High P ( phosphate and Potassium ) + Uric acid 2.Low Calcium ( the phosphate bind the calcium so more phosphate with bind more Ca making it low ) Manage with: Fluids Allopurinol + Rasburcase “ lowers uric acid “ Monitor the Arrhythmia’s ( because of Ca + K abnormality )