Non-Malignant Granulocyte Disorders Flashcards

1
Q

How are WBC values different in newborns?

A

Newborns will have a higher WBC count, Neutrophil %, and absolute count

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2
Q

What is referred to as ‘reverse ratio’ or ‘inverted diff’?

A

It is the fact that by one year of age, the lymphocyte % is almost double the neutrophil %

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3
Q

What the differences in the CBC of a person older than 65 compared to one younger than 65?

A

People older than 65 have a slightly lower WBC. RBC, HGB, and PLTS and have a slightly higher MCV

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4
Q

What are some benign reasons for an absolute neutrophilia?

A

Stress, trauma, labour, strenuous exercise, shock, burns, or an increase in epinephrine

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5
Q

What pathological condition causes absolute neutrophilia?

A

Infection

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6
Q

What is a left shift?

A

An increased number of immature cells - which indicates infection

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7
Q

What types of cells are usually increased in a left shift?

A

Bands, metamyelocytes (and possibly myelocytes)

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8
Q

What is a leukemoid reaction?

A

A reactive leukocytosis above 50 x 10^9/L with neutrophilia and a marked left shift

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9
Q

What kinds of cells are present in a leukemoid reaction?

A

Bands and often metas/myelos with a rare Pro or Blast

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10
Q

What causes leukemoid reactions?

A

Severe and/or chronic infection (e.g. TB, pneumonia)
Metabolic disease
Inflammation
Response to a malignancy

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11
Q

What is meant by a Leukoerythroblastic picture?

A

The presence of immature neutrophils, nucleated RBCs, and teardrop RBCs in the same sample

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12
Q

What kind of issue do Leukoerythroblastic reactions point to?

A

The possibility of space-occupying lesion in the bone marrow (e.g. metastatic tumor, fibrosis, lymphoma, leukemia)

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13
Q

What are 5 causes of absolute neutropenia?

A
  1. Increased rate of removal or destruction
  2. Decreased production or ineffective hematopoiesis
  3. Decreased ratio of circulating vs marginal pool
  4. Depletion of BM storage pool
  5. BM suppression - decreased production/impaired release
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14
Q

What are some causes of Eosinophilia?

A

Allergies (asthma)
Parasitic infection
Some auto-immune disorders (HIV)
Fungal infections
Some malignancies (ALL)

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15
Q

What are some non-malignant causes of basophilia?

A

Bee stings
Food/drug hypersensitivity
Chronic infections
Hypothyroidism
Chronic inflammation
Radiation therapy

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16
Q

What is a malignant cause of basophilia?

A

Chronic myelogenous leukemia

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17
Q

What kinds of acquired granulocyte nuclear anomalies are there?

A

Hyposegmentation
Hypersegmentation
Pyknotic & Necrobiotic forms

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18
Q

What kinds of acquired granulocyte cytoplasmic anomalies are there?

A

Toxic granulation
Degranulation
Vacuolization (with or without engulfed matter)
Dohle bodies

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19
Q

What can cause hypersegmented nuclei?

A

Chronic infections
Megaloblastic anemia
Drugs

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20
Q

What can cause hyposegmented nuclei?

A

Myelodysplastic syndromes
Asynchrony of nuclear maturation (very clumped chromatin with no segmentation)

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21
Q

Where are mitotic cells usually only seen?

A

In the bone marrow

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22
Q

Should you count mitotic cells in a diff?

A

No, just comment if several are seen

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23
Q

What kind of reactive morphologic changes in neutrophils are there?

A

Toxic granulation, Dohle bodies, and cytoplasmic vacuoles

24
Q

What is toxic granulation a response to?

A

Infection/inflammation

25
Q

Is toxic granulation clinically significant?

A

Yes, it’s a marker for inflammation

26
Q

Do you report toxic granulation?

A

Yes with WBC morphology (occ/some/many)

27
Q

What does toxic vacuolization in neutrophils indicate?

A

Phagocytosis, may contain bacteria and other material
Often seen with toxic granulation

28
Q

Do you report toxic vacuolization?

A

Yes with WBC morphology (occ/some/many)

29
Q

What do Dohle bodies look like?

A

Pale blue, oval inclusions at periphery only in neutrophils

30
Q

What are Dohle bodies?

A

Remnants of ribosomal RNA

31
Q

What conditions are Dohle bodies associated with?

A

Bacterial infection
Sepsis
Pregnancy

32
Q

Do you report Dohle Bodies?

A

Yes with WBC morphology (occ/some/many)

33
Q

What is an LE cell?

A

A mature neutrophil which has phagocytized a spherical, homogenous-appearing inclusion

34
Q

What is the inclusion that is inside an LE cell?

A

Nuclear material of degenerating leukocytes coated with an antinuclear antibody

35
Q

Are LE cells seen in a PBS normally?

A

No, unless the sample is manipulated. It’s only naturally seen in body fluids

36
Q

Why does the inclusion in an LE cell appear homogenous?

A

Because the protein in the engulfed nucleus is depolymerized by the antibody

37
Q

Is an Auer rod a malignant change?

38
Q

In which condition are Auer rods typically seen?

A

Only in blasts (in myeloblasts only, not lymphoblasts) and promyelocytes in acute leukemia

39
Q

What are Auer rods?

A

Fused primary granules

40
Q

What do Auer rods look like?

A

Azurophilic rods

41
Q

How do you report Auer rods?

A

With WBC morphology (occ/some/many)

42
Q

What is the characteristic WBC morphology in Pelger-Huet Anomaly?

A

Hyposegmentation of neutrophil nucleus

43
Q

What type of genetic disorder is Pelger-Huet Anomaly?

A

Autosomal Dominant

44
Q

What symptoms are associated with Pelger-Huet Anomaly?

A

It’s asymptomatic

45
Q

What is the difference between heterozygous and homozygous Pelger-Huet Anomaly?

A

The heterozygous state has a bi-lobed nucleus and the homozygous state has a round/oval nucleus with no segmentation

46
Q

How many neutrophils are affected in Pelger-Huet anomaly?

47
Q

In which kinds of conditions are pseudo-Pelger-Huet forms seen?

A

Can be induced by certain drugs
HIV, TB, mycoplasma pneumonia, and severe bacterial infections
Secondary to MDS, acute leukemias, and chronic myeloproliferative disorders

48
Q

What are the differences between true vs pseudo Pelger-Huet forms?

A

In true PH, all WBCs are affected whereas in pseudo PH, usually only neutrophils are affected and they are accompanied by other abnormal changes

49
Q

When do you report Pelger-Huet forms in the comments?

A

If all the neutrophils are affected with classic bi-lobed or single-lobed forms

50
Q

When you report hyposegmented neutrophils in the WBC morph section?

A

If the neutrophils have mature chromatin but no segmentation

51
Q

What type of genetic disorder is Alder-Reilly Anomaly?

A

Autosomal recessive

52
Q

What is the key characteristic of Alder-Reilly Anomaly?

A

Abnormally large metachromatic granules in the cytoplasm of: granulocytes, monocytes, and lymphocytes

53
Q

What is the cause of the granules in Alder-Reilly Anomaly?

A

Mucopolysaccharide deposits

54
Q

Is leukocyte function affected in Alder-Reilly Anomaly?

55
Q

What type of genetic disorder is May-Hegglin Anomaly?

A

Autosomal dominant

56
Q

What are the key characteristics of May-Hegglin Anomaly?

A

Leukopenia with large basophilic inclusions
Variable thrombocytopenia with giant forms