W9- WBC DISORDERS Flashcards

1
Q

What is it called when these abnormal cells are present both in the circulation and bone marrow

A

Leukemia

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

What is it called when these abnormal cells are present ONLY in the bone marrow

A

Aleukemic leukemia

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

What are the risk factor in developing leukemia

A
  • Family history (genetic abnormalities, trisomy 21)
  • occupational hazards (benzene exposure carcinogenicin nature)
  • Ionizing radiation (rad dept)
  • Immunologic deficiency (
  • Autoimmune disease (e.g., SLE)
  • Idiopathic (Leukemia)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Criteria for diagnosing leukemia

A

WHO: >20% blasts

FAB french american british: >30% blasts

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

In this disorder, the leukocyte count is variable

  • DECREASE LAP/NAP score because of inactivity
  • leukocytosis (50-300,00 cumm)
A

leukemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q
  • Excessive leukocytic response
  • leukocytosis (50-100,000 cumm)
  • INCREASE LAP/NAP score because of an inflammation
A

Leukemoid reaction

-Increase LAP/ NAp cause by premature release of the maturation stage in the bone marrow towards the circulation

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

that involves GEMM(granulocyte, erythrocyte, monocyte, and megakaryocyte) also known as myeloproliferative

A

Myeloid

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

involving the B or T cell and may be leukemia or lymphoma (solid tumor)

A

lymphoid

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

the blast is greater than 30%

-days to weeks (3 months)

A

Acute leukemia

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

the blast is less than 10%

-more than a year (1-2 years)

A

Chronic leukemia

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

what classification of leukemia is Rapid and progressive

  • Affects all ages
  • Elevated proliferative rates
  • Blast are predominant
A

Acute leukemia

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

what classification of leukemia is Insidious

  • Adults are affected
  • Lower proliferative rates
  • Mature cells are predominant
A

Chronic leukemia

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

What is the most common type of leukemia for adults ?

-there are presence of AUER RODS

A

Acute myeloblastic leukemia

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

What is it called when Auer rods are present in a lot of cell ?

A

Faggot cell

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

What stain is use in differentiating AML (acute myelocytic leukemia) from ALL ( acute lymphoblastic leukemia) , it is present in granulocyte and monocyte

A

Peroxidase

-bluish black

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

of all the granulocyte present, the eosinophil is resistant. there is still an activity even if there is a presence of sodium cyanide in the peroxidase stain. that’s why your eosinophil of leukemia will be diagnose through this stain

A

Cyanide-resistant peroxidase (CRP)

-brown and granular

17
Q

it stains lipid component of cell

- it differentiate AML from ALL

A

Sudan black b (SBB)

- blask

18
Q

the stain is chroloacetate

-it differentiates granulocytic from monocytic leukemia

A
Specific esterase (SE)
-blue
19
Q

Differentiates monocytic from granulocytic leukemia

A

Non-specific esterase (NSE)

-bright red

20
Q

it stains glycogen and related substances anything carbohydrates -use in diagnosing your erythrocytic leukemia

A

periodic acid Schiff (PAS)

- reddish pink periphery

21
Q

uses tartaric acid

-helpful in diagnosis of Hairy cell leukemia

A
Acid phosphatase (AP) 
- orange red
22
Q

present in lymphoid lineage

differentiates ALL from AML

A

Terminal Deoxynucleotidyl transferase (TDT)

-fluoresecence

23
Q
A

AML - M1

24
Q
  • WITH MATURATION
  • <20% are monocytic lineage
  • > 3% of the blast stain POSITIVE with MPO and SBB
  • chromosome abnormality : t(8, 21)
  • the most common subtype of leukemia
  • may have Auer rods (altered primary granules )
A

AML- M2

25
Q
  • PROMYELOCYTIC leukemia
  • > 30% of blast are type I, II and III
  • abnormal promyelocyte Multiple auer rods (Faggot cell)
  • chromosome abnormality: t(15;17)
  • Associated with DIC (disseminated intravascular coagula) and hemorrhage
A

AML-M3

26
Q

-MYELOMONOCYTIC LEUKEMIA or naegeli monocytic leukemia

  • > 30% of the blast are type I and II with promonocytes
  • Peripheral monocytes: >5x10^9/L
  • High serum lysozyme
A

AML- M4

  • most common subtype of AML leukemia of the myeloid lineage
  • stains with (SE) specific esterase and (NSE) Nonspecific esterase,SBB, MBO
27
Q
  • MONOCYTIC LEUKEMIA or Schillings leukemia
  • > 30% monoblast, promonocyte, and myeloblasts
  • m5a: predominantly monoblast (>80%)
  • m5b: predominantly promonocytes (<80%)
A

AML-M5

-stains with (NSE) non specific esterase

28
Q
-ERYTHOLEUKEMIA or diguglielmo syndrome
bone marrow is hypercellular
->50% are erythroblast
->30% are types I, II and III blast
-immunophenotype: positive for glycophorin A
A

AML-M6

-positive for (PAS) periodic acid Schiff

29
Q
  • MEGAKARYOTIC LEUKEMIA
  • > 30% are megakaryoblast with myeloblasts
  • accompanied by atypical megarkaryocytes and the BONE marrow is often fibrotic
  • immunophenotype: Glycoproteins 1b95 (responsible for the adhesion of the platelets) and 2b llb/ 3bllIa (responsible for the aggregation of platelet to platelet )
  • EM ultracytochemical identifaction: Platelet peroxidase
A

AML-M7

  • it requires immunocytochem staining for accurate diagnosing
  • Factor A or 8? stain or antihemophilic factor
30
Q

What is the most common type of leukemia in CHILDREN

-positive for terminal Deoxynucleotidyl transferase

A

Acute lymphoblastic leukemia