Leukocyte Disorders part 1 & 2 Flashcards

(54 cards)

1
Q

Quantitative term in terms of decrease RBC, WBC, and platelets?

A

Pancytopenia

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2
Q

Absolute count of neutrophilia?

A

> 7.0 - 8.0 x 10^9/L

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3
Q

Treatment for neutrophilia?

A

Corticosteroids and lithium

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4
Q

Usually transient or short-term increase of WBC?

A

Physiologic neutropenia

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5
Q

Most common type of leukopenia?

A

Neutropenia

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6
Q

Felty’s syndrome is due to?

A

Neutropenia

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7
Q

A drug that induced neutropenia?

A

Amidopyrine and cephalosphorins

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8
Q

5 clinical manifestations of Felty’s syndrome?

A

“SANTA”
Spenomegaly
Anemia
Neutropenia
Thrombocytopenia
Arthritis

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9
Q

Absolute count of eosinophilia?

A

0.4 x 10^9/L

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10
Q

Increased when there is an allergic reactions, pulmonary disorders, gastrointestinal disorders, infections such as scarlet fever, HIV infection, and infestation of tissue-invading parasites?

A

Eosinophilia

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11
Q

Difficult to detect using routine differentials and total leukocyte count?

A

Eosinopenia

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12
Q

This is caused by ACTH administration or Thorn’s test?

A

Eosinopenia

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13
Q

This is a common cause in the presence of malignant myeloproliferative neoplasm?

A

Basophilia

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14
Q

This is associated and relatively a recovery from neutropenia?

A

Monocytosis

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15
Q

Absolute monocyte count of monocytosis?

A

> 0.9 x 10^9/L

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16
Q

A very rare condition of leukopenia that is found in patients receiving steroid therapy?

A

Monocytopenia

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17
Q

Hallmark of pernicious anemia?

A

Hyepersegmented neutrophil

> 2-5 lobes
polycyte and macropolycyte

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18
Q

Termed as disappearance of nucleus or smaller nucleus?

A

Pyknocyte

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19
Q

Virocyte or Atypical Lymphocyte is also known as?

A

Downey Type Cell and Turk Irritation Cell

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20
Q

This cell is activated to respond a viral infection?

A

Atypical lymphocyte

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21
Q

This cell is seen in acute myeloid leukemia (AML)

A

Reider cell

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22
Q

Usually signs of degeneration in severe infections, chemical poisoning, and leukemia?

A

Vacuolated cell

23
Q

This lymphocyte abnormality is seen in chronic lymphocytic leukemia (CLL)

A

Basket cell or Smudge cell

24
Q

Cell that can be seen in patients having Systemic Lupus Erythematosus?

25
PMN which had engulfed the nuclear material of another PMNs or a lymphocyte?
L.E. cell
26
A condition in which monocyte engulfed the nucleus of a lymphocyte or maybe whole lymphocyte itself and this strongly exhibits nucleophagocytosis?
Tart cell
27
This cell exhibits hairy cell leukemia and a type of lymphocyte with hair like cytoplasmic projections?
Hairy cell
28
This cell is commonly seen in a condition called Sezary syndrome and Mycosis fungoides?
Sezary cell
29
This abnormal inclusion body that is classified as always pathological and is spindle in shape and red-purple in color?
Auer bodies/Rods
30
Classified as azurophilic granules?
Auer bodies
31
This inclusion bodies are frequently seen in aplastic anemia and in myelosclerosis?
Toxic granules
32
Inclusion body that stains blue-gray and is usually seen in the periphery of the cytoplasm of neutrophils?
Dohle-Amato bodies
33
Remnants of free ribosomes and mostly seen in bacterial infections, severe burns, exposure to cytotoxic agents, and complicated pregnancies?
Dohle-Amato bodies
34
Inclusion body that is found in the cytoplasm if multiple myeloma and plasma cells after therapy with amidine drugs?
Snapper-Scheid bodies
35
Gamma-globulins bodies that gave a grape or berry or morula cell appearance?
Russel or Fuch's bodies
36
2 groups of leukocyte disorders?
Non-Neoplastic Disorders and Neoplastic and Related Disorders
37
Disorder of nucleus associated with abnormal DNA synthesis and is seen in megaloblastic anemia, it also causes shift to the right?
Hypersegmented neutrophil
38
Decrease segmentation of neutrophil and usually has "pinceness appearance"
Pelger-Guet anomaly
39
This is also known as true or congenital PHA and lamin-B receptor is defected.
Pelger-Huet anomaly
40
Pelger-Huet anomaly is commonly seen in conditions such as?
CML (chronic myelogenous leukemia) and CMDS (chronic myeloproliferative disorder or sydrome)
41
Anomaly that affect all WBC lineage in terms of nuclear shape and chromatin structure?
True-Pelger-Huet anomaly
42
Another type of anomaly that only affects the nucleus of neutrophils and has a less dense nuclei?
Pseudo-Pelger-Huet anomalu
43
Cytoplasm disorder that is usually seen in hunter's syndrome and hurter's syndrome?
Alder-Reily anomaly
44
This has large peroxidase lysosomes inclusions that are deficient in enzymes for phagocytosis. This is also associated with albinism as clinical condition?
Chdiak-Higashi syndrome
45
This is caused by the mutation in the MYH9 gene?
May-Hegglin anomaly
46
Functional disorder in which random movement of phagocytes is normal, but directional motility is impaired.
Job's syndrome
47
Functional disorder of leukocyte that is characterized by both random and directed movement of the cells are defective.
Lazy Leukocyte syndrome
48
Intracellular killing of granulocyte is then defective and usually seen in childhood?
Chronic Granulomatous disease
49
Type of Gaucher's disease characterized by a defect or change in acute neuronopathic and is associated with infancy?
Type 2 Gaucher's disease
50
Type of Gaucher's disease that is characterized by sub-acute neuronopathic and is associated with childhood type?
Type 3 Gaucher's disease
51
It is an inherited leukocyte disorder in which caused by a mutation in the lamin-B receptor?
Pelger-Huet anomaly
52
It is loss of both T and B cells function and is an autosomal recessive disorder?
Swiss-Type Aggamaglobulinema
53
Decrease T-cell production and associated in rare childhood disease and which affects the brain and other parts of the body?
Ataxia Talengiectasia
54
The expected CBC results for women in active labor would be?
High total WBC count with a slight shift to the left in neutrophils