W9- WBC DISORDERS Flashcards

(30 cards)

1
Q

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

A

Leukemia

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2
Q

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

A

Aleukemic leukemia

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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)
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4
Q

Criteria for diagnosing leukemia

A

WHO: >20% blasts

FAB french american british: >30% blasts

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5
Q

In this disorder, the leukocyte count is variable

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

leukemia

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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

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7
Q

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

A

Myeloid

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8
Q

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

A

lymphoid

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9
Q

the blast is greater than 30%

-days to weeks (3 months)

A

Acute leukemia

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10
Q

the blast is less than 10%

-more than a year (1-2 years)

A

Chronic leukemia

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11
Q

what classification of leukemia is Rapid and progressive

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

Acute leukemia

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12
Q

what classification of leukemia is Insidious

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

Chronic leukemia

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13
Q

What is the most common type of leukemia for adults ?

-there are presence of AUER RODS

A

Acute myeloblastic leukemia

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14
Q

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

A

Faggot cell

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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

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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
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 )
25
- 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
AML-M3
26
-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
AML- M4 - most common subtype of AML leukemia of the myeloid lineage - stains with (SE) specific esterase and (NSE) Nonspecific esterase,SBB, MBO
27
- MONOCYTIC LEUKEMIA or Schillings leukemia - >30% monoblast, promonocyte, and myeloblasts - m5a: predominantly monoblast (>80%) - m5b: predominantly promonocytes (<80%)
AML-M5 | -stains with (NSE) non specific esterase
28
``` -ERYTHOLEUKEMIA or diguglielmo syndrome bone marrow is hypercellular ->50% are erythroblast ->30% are types I, II and III blast -immunophenotype: positive for glycophorin A ```
AML-M6 | -positive for (PAS) periodic acid Schiff
29
- 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
AML-M7 - it requires immunocytochem staining for accurate diagnosing - Factor A or 8? stain or antihemophilic factor
30
What is the most common type of leukemia in CHILDREN -positive for terminal Deoxynucleotidyl transferase
Acute lymphoblastic leukemia