Hema exam reviewer Flashcards

1
Q

Lymphocytes disorders

Deficiency of hexosaminidase A

A

Tay-sachs disease

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2
Q

Lymphocytes disorders

Reduced Immunoglobulins production in blood

A

Bruton Agammaglobulinemia

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3
Q

Lymphocytes disorders

Reduced production of Ig due to overactivity of t8 cells

A

Common variable hypogammaglobulin

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4
Q

Lymphocytes disorders

Underdevelopment of thymus

A

Nezelof’s syndrome

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5
Q

Lymphocytes disorders

Deletion of small piece of chromosome 22

A

Di Geroge’s syndrome

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6
Q

Lymphocytes disorders

Loss of Both T and B cells function

A

Swiss-type agammaglobulinemia

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7
Q

Lymphocytes disorders

Failure of T cell response

Only IgA and IgG are present, IgM is absent

A

Wiscott-aldrich syndrome

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8
Q

Lymphocytes disorders

Decreased T cell production
Spider veins

A

Ataxia Telangiectasia

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9
Q

Monocyte macrophage disorder

Deficiency of glucocerebrosidase

A

Gaucher’s disease

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10
Q

Most common lysosomal lipid storage disease

A

Gaucher’s disease

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11
Q

Monocyte macrophage disorder

Deficiency of sphingomyelinase

A

Niemann-Pick disease

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12
Q

Monocyte macrophage disorder

Macrophage with cholesterol overload due to increase in foam cells

A

Schiller-Christian disease

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13
Q

Function disorder

Random movement of phagocytes is NORMAL
Directional motility is IMPAIRED

A

Job’s syndrome

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14
Q

Function disorder

BOTH random and directional motility is impaired

A

Lazy leukocyte syndrome

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15
Q

Function disorder

Intracellular mechanism of granulocyte is defective

A

Chronic Granulomatous Disease

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15
Q

Function disorder

Have half the normal C3 Activity
Homozygous carriers fail to opsonize bacteria

A

Congenital C3 Deficiency

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16
Q

Function disorder

MPO is decreased or absent in PMN and monocytes

A

Myeloperoxidase deficiency

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17
Q

Nucleus disorder

Abnormal DNA synthesis

A

Hypersegmented neutrophil

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18
Q

Nucleus disorder

Decreased segmentation in neutrophil

Pince nez appearance

Defect mutation in Lamin B

A

Pelger-Huet anomaly

19
Q

Nucleus disorder

Has less dense nuclei with hypo granular cytoplasm

A

Pseudo Pelger-Huet anomaly

20
Q

Cytoplasm disorder

Accumulation of degraded mucopolysaccharides

A

Alder-reily anomaly

21
Q

Cytoplasm disorder

Has large peroxidase lysosomes inclusions that are deficient in enzymes for phagocytosis

A

Chediak-Higashi syndrome

22
Q

Cytoplasm disorder

Dohle bodies, Thrombocytopenia, Giant platelets, and leukopenia

Mutation in MYH9 gene

A

May-Hegglin anomaly

23
Q

Normal cell with a biconcave disk shape with increased surface

24
Cell with central area of hemoglobin surrounded by colorless area and a peripheral ring Caused by excessive cholesterol in the membrane or hemoglobin distribution imbalance
Targe Cells / Mexican Hat / Bull's eye cells/ Codocytes
25
RBC that lacks the central pallor Caused by spectrin deficiency
Spherocyte
26
Abnormal RBC with spines, spicules, or thorny projection Abnormal membrane defect caused by an increase spingomyelin and decrease in cholesterol and phospholipid
Acanthocyte / Spurr Cell / Thorny cell
27
Pocket book roll Cell membrane is folded
Biscuit cell / Folded RBC
28
Cell with irregularly spaced blunt processes, resembles crenated RBC Abonrmal lipid content of the membrane
Burr Cell
29
Cell with eccentric vacuoles due to the plucked-out HEINZ BODIES Defect is G6PD deficiency resulting to accumulation of Heinz bodies
Blister cell / Bite Cell
30
RBC with blunt or pointed, short projections that are usually evenly spaced over the surface of cell Have evenly spaced round projections; central pallor are present Defects: ATP deficiency due to prolong storage of anticoagulated blood Due to abnormal lipid content of the membrane
Echinocyte / Crenated Cell / Sea Urchin Cell
31
Cells appear in the shape of a teardrop or pear Abnormal maturation, squeezing and fragmentation during splenic passage
Tear drop cell / Dacrocyte
32
Sausage - shaped, oval, pencil form, egg shape, cigar - shaped Abnormal membrane due to defective spectrin and deficiency in band protein 4.1
Elliptocyte/Ovalocyte
33
Shape shows thin, elongated, pointed ends and will appear crescent shaped; lack a central pallor S,V,L shaped Crescent shape cell due to abnormal aggregation of Hb S which gives a tendency for the cell to assume the shape
Sickle cell / Drepanocyte / Menisocyte
34
Triangular shape, defragmented form Defects in cell fragmentation due to TRAUMA caused by PHYSICAL AND MECHANICAL AGENTS
Schistocyte / Helmet cell
35
Characterized by an elongated or slit-like area of central pallor Caused by osmotic changes due to cation imbalance
Stomatocyte / Hydrocyte / Mouth cells
36
Blue berry bagel appearance Punctuate basophilia due to deficiency in pyrimidine 5' - nucleotidase enzyme Content is precipitated RNA / Remnants of RNA
Basophilic stippling of RBC
37
Basophilic stippling of RBC most common associated disease
LEAD POISONING and PICA
38
Composed of Chromatin material (DNA) Not commonly seen in normal erythrocytes because it is pitted by splenic macrophages
Howell-Jolly bodies
39
Indicative of faulty IRON utilization in the synthesis of hemoglobin Composed of FERRIC IRON
Pappenheimer bodies / Siderotic granules
40
Indicative of disturbed hemoglobin synthesis and breakdown NOT VISIBLE TO WRIGHT STAIN Content is DENATURED HEMOGLOBIN
Heinz Bodies
41
Looped or figure of eight shape or ring with red-purple color arranged in linear pattern Indicative of DEFECTIVE REGENERATIVE ACTIVITY Composed of Remnant of mitotic spindles or microtubules
Cabot Rings
42
Caused by instability of Hb H Content is precipitated of Beta globin chains of hemoglobin
Hemoglobin H inclusion
43
Acute post hemorrhagic anemia Hemolytic anemia Marrow hypoplasia Aplastic anemia Marrow infiltration Kidney and liver disease Endocrine deficiencies Anemia of chronic disease
Normochromic normocytic anemia
44
Disorders of iron metabolism IDA Anemia of chronic disease Congenital hypochromic
Microcytic anemia
45
Cobalamin Deficiency (B12 def) Decreased ingestion Competitive parasite Fish tapeworm infestation Folate deficiency Lack of vegetable Alcoholism
Macrocytic anemia
46