Hematology Flashcards

1
Q

What is a neutrophil?

A

The Phagocyte
(Has anti-microbials, most abundant)

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2
Q

What is an Eosinophil?

A

The Parasite Destroyer
Also, an allergy inducer

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3
Q

What is a Basophil?

A

The Allergy Helper
(IgE receptor => histamine release)

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4
Q

What is a Monocyte?

A

The Destroyer = the MP
(Hydrolytic enzymes, coffee-bean nucleus)

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5
Q

What is a Lymphocyte?

A

The Warrior
= T, B, NK cells

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6
Q

What is a Platelet?

A

The Clotter
(No nuclei, smallest cells)

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7
Q

What is a Blast?

A

Baby hematopoietic cell

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8
Q

What is a Band?

A

Baby neutrophil

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9
Q

What does high WBC and high PMNs tell you?

A

Stress demargination

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10
Q

What does high WBC and <5% blasts tell you?

A

Leukemoid reaction
Seen in burn patients
(Extreme demargination, looks like leukemia)

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11
Q

What does high WBC and >5% blasts tell you?

A

Leukemia

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12
Q

What does high WBC and bands tell you?

A

Left shift => infection present

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13
Q

Hat does high WBC and B cells tell you?

A

Bacterial infection

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14
Q

What diseases have high eosinophils?

A

NAACP
- Neoplasm (lymphoma)
- Allergy/Asthma
- Addison’s disease (no cortisol -> relative eosinophilia)
- collagen vascular disease
- parasites

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15
Q

What disease have high monocytes? (>15%)

A

“STELS”
- syphilis: chancre, rash, warts
- TB: hemoptysis, night sweats
- EBV: teenager sick for a month
- Listeria: baby who is sick
- Salmonella: food

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16
Q

What do high reticulocytes (>1%) tell you?

A

RBC being destroyed peripherally

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17
Q

What is poikilocytosis?

A

Different shapes

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18
Q

What is anisocytosis?

A

Different sizes

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19
Q

What is the RBC lifespan?

A

120 days

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20
Q

What is the platelet lifespan?

A

7 days

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21
Q

What does “-penia” tell you?

A

Low levels
(Usually d/t virus or drugs)

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22
Q

What does “-cytosis” tell you?

A

High levels

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23
Q

What does “-cythemia” tell you?

A

High levels

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24
Q

What is the difference between plasma and serum?

A

Plasma: no RBC
Serum: no RBC or fibrinogen

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25
What is a Chronic granulomatous disease?
NADPH oxidase deficiency -> recurrent Staph/Aspergillus infections (Nitro blue Tetrazolium stain negative)
26
What does MPO deficiency cause?
Catalase pos infections
27
What is Chediak-Higashi?
Lazy leukocyte syndrome (Lysosomes are slow to fuse around bacteria)
28
What organ can make RBCs if the long bones are damaged?
Spleen (Leading to splenomegaly)
29
What causes a shift to the right in the Hb curve?
“all CADETs face right” - elevated CO2 - Acid/Altitude (= low pH) - elevated 2,3-Dpg - Exercise - Temp
30
How does CO poison Hb?
Competitive inhibitor of O2 on Hb Cherry-red lips Pinkish skin hue
31
How does cyanide poison Hb?
Non-competitive inhibitor of O2 on Hb Almond breath
32
What is MetHb?
Hb w/ Fe3+
33
What is acute intermittent porphyria?
Elevated porphyrin Elevated urine d-ALA Elevated porphobilinogen Abdominal pain Neuropathy Red urine
34
What is porphyria cutanea tarda?
D/t sunlight Skin blisters w/ porphyrin deposits Wood’s
35
What is erythrocytic protoporphyria?
Porphyria cutanea tarda in a baby
36
What is sickle cell disease?
Homozygous HbS (beta chain mutation at position 6: Glu -> Val) Vaso-occlusion Necrosis Dactylitis (painful fingers/toes) at 6 mo Protects against malaria
37
What is Sickle cell trait?
Heterozygous HbS Painless hematuria Sickle with extreme hypoxia (Cannot be pilot, fireman, diver)
38
What is HbC disease?
Hb mutation in beta chain at position 6 (Glu -> Lys) Still charged => no sickling
39
What is alpha thalassemia?
1 deletion: normal 2 deletions “trait”: microcytic anemia 3 deletions: hemolytic anemia, HbH (= 4 beta chains) 4 deletions: hydrops fetalis, HbBart (= 4 gamma chains)
40
What is beta thalassemia?
1 deletion = “beta minor” = HbA2 + HbF 2 deletions = “trait/intermedia/major” = only HbA2 and HbF => hypoxia at 6 mo
41
What is Cooley’s anemia?
See w/ beta-thalassemia major (no HbA => excess RBC production) Baby making blood from everywhere => frontal bossing, hepatosplenomegaly, long extremities
42
What is Virchow’s triad?
Thrombosis risk factors: - turbulent blood flow “slow” - hypercoaguable “sticky” - vessel wall damage “escapes”
43
What does acute hypoxia cause?
Shortness of breath
44
What does chronic hypoxia cause?
Clubbing of fingers/toes
45
What is intravascular hemolysis?
RBC destroyed in blood vv. -> low haptoglobin
46
What is extravascular hemolysis?
RBC destroyed in spleen (problem w/ RBC membrane) => splenomegaly
47
What enzymes need lead (Pb)?
d-ALA dehydratase Ferrochelatase
48
What does EDTA bind?
Any heavy metals with 2+ charge (Lead, Iron, Calcium, Magnesium)
49
What disease has a smooth philtrum?
Fetal alcohol syndrome
50
What disease has a long philtrum?
William’s Syndrome (Deletion on chromosome 7)
51
What disease has sausage digits?
Pseudo-hypoparathyroidism Psoriatic arthritis
52
What disease has 6 fingers?
Trisomy 13 (Patau Syndrome)
53
What disease has 2-jointed thumbs?
Diamond-Blackfan
54
What disease has painful fingers? (= “dactylitis”)
Sickle cell disease
55
What are the Microcytic Hypochromic anemias?
“FASTT LEAD” - Fe deficiency = elev TIBC, menses, GI bleed, koilonychia - Anemia of chronic disease = decr TIBC - Sideroblastic anemia = decr d-ALA synthase, blood transfusions - alpha-Thalassemia = AA, Asians (Chr 16 deletion) - beta-Thalassemia = Mediterraneans (Chr 11 point mutation) - Lead poisoning = decr d-ALA dehydratase, decr ferrochelatase, blue line on x-ray, eating old paint chips
56
What are the megaloblastic anemias?
Vit B12 deficiency Folate deficiency Alcohol
57
Megaloblastic anemia: Vit B12 deficiency
d/t tapeworms, vegans, Type A gastritis, pernicious anemia
58
Megaloblastic anemia: Folate deficiency
d/t old food, glossitis
59
Megaloblastic anemia: Alcohol
Seen w/ fetal alcohol syndrome - smooth philtrum - stuff doesn’t grow
60
What are the Intravascular Hemolytic anemias?
G6PD deficiency Cold autoimmune Problem w/ IgM
61
Intravascular Hemolytic anemia: G6PD deficiency
d/t sulfa drugs, moth balls, fava beans See a sudden drop in Hb
62
Intravascular Hemolytic anemia: Cold autoimmune
Seen with: - mononucleosis - mycoplasma infections - RBC agglutination
63
What are the Extravascular Hemolytic anemias?
Spherocytosis Warm autoimmune Paroxysmal cold autoimmune Sickle cell anemia Problem w/ IgG
64
Extravascular Hemolytic anemia: Spherocytosis
Defective spherin or ankyrin Pos osmotic fragility test
65
Extravascular Hemolytic anemia: Warm autoimmune
Anti-Rh Ab Dapsone PTU Anti-malarials Sulfa drugs
66
Extravascular Hemolytic anemia: Paroxysmal cold autoimmune
Bleeds after cold exposure Donath-Landsteiner Ab
67
Extravascular Hemolytic anemia: Sickle cell anemia
Crew haircut on X-ray Avascular necrosis of femur Short fingers
68
What are the Production Anemias?
Diamond-Blackfan Aplastic anemia
69
Production anemias: Diamond-Blackfan
No RBCs 2-jointed thumbs
70
Production anemias: Aplastic anemias
Pancytopenia Autoimmune d/t benzene, AZT, CAM, radiation
71
What is basophilic stippling?
Lots of immature cells Incr mRNA d/t lead poisoning
72
What is a burr cell (=echinocyte)?
Seen in: - Pyruvate kinase deficiency - liver disease - post-splenectomy
73
What is a Bite cell (= basket cell)?
Seen in: - unstable Hb inclusions (such as G6PD deficiency)
74
What is Cabot’s ring body?
Seen in: - vit B12 deficiency - lead poisoning
75
What is a Doehle body?
Seen in: PMN leukocytosis - infection - steroids - tumor
76
What is a Drepanocyte?
Seen in: Sickle cell anemia
77
What is a Helmet cell?
Fragmented RBC Seen in: hemolysis - DIC - HUS - TTP
78
What is a Heinz body?
Hb precipitates and sticks to cell membranes Seen in G6PD deficiency
79
What is a Howell-Jolly body?
Spleen or bone marrow should have removed nuclei fragments - hemolytic anemia - spleen trauma - cancer
80
What is a Pappenheimer body?
Iron precipitated inside cell Seen in: sideroblastic anemia
81
What is a Pencil cell (= cigar cell)?
Seen in iron deficiency anemia
82
What is a Rouleaux formation associated with?
Multiple myeloma
83
What is a Schistocyte?
Broken RBC Seen in: DIC & artificial heart valves
84
What is a sideroblast?
Macrophages pregnant w/ Fe (d/t genetic or multiple transfusions)
85
What is a spherocyte?
Old RBC
86
What is a spur cell (=acanthocytes)?
RBCs covered in lipids (High serum lipids)
87
What is a stomatocyte associated with?
Liver disease
88
What does a target cell (= codocyte) indicate?
Less Hb - thalassemias - Fe deficiency
89
What is a teardrop cell (= dacrocyte)?
RBCs squeezed out of bone marrow Seen in hemolytic anemia, any diseases that make RBCs come out of bone marrow too fast)
90
What is the purpose of the clotting cascade?
How the body stops bleeding
91
What clotting factors use Vitamin K as a cofactor?
2, 7, 9, 10, protein C, protein S
92
What do platelet problems cause?
Bleeding from skin and mucosa
93
What do clotting factor problems cause?
Bleeding into cavities
94
What causes increased PTT and bleeding time?
Von Willebrand disease Lupus
95
What is Bernard-Soulier?
Baby w/ bleeding from skin and mucosa Big platelets Low Gp 1b
96
What is Glanzmann’s?
Baby w/ bleeding from skin and mucosa Low Gp 2b/3a
97
How does Factor 13 deficiency present?
Umbilical stump bleeding (1st time baby has to stabilize a clot)
98
What is Factor V Leiden?
Protein C can’t break down Factor V => more clots
99
How does Von Willebrand disease present?
Heavy menstrual bleeding Easy bruising Petechiae Bleeding of gums Prolonged bleeding from minor injuries
100
What are the types of vWD?
Type 1 (AD): decr vWF production Type 2 (AD): decr vWF production (pos Ristocetin aggregation test) Type 3 (AR): no vWF
101
What is a hemophilia A?
Defective Factor VIII (<40% activity) => bleed into cavities (head, abdomen, etc.)
102
What is Hemophilia B?
Factor IX deficiency => bleed into joints (knee, etc.)
103
What diseases have low LAP?
CML PNH
104
What has high LAP?
Leukemoid reaction
105
What is the difference between acute and chronic leukemias?
Acute - started in bone marrow - squeezes RBC out of marrow Chronic - started in periphery - not constrained => will expand
106
What is the difference between myeloid and lymphoid leukemias?
Myeloid - elev RBC - elev WBC - elev platelets - elev macrophages - decr lymphocytes => do bone marrow biopsy Lymphoid - elev NK cells - elev T cells - elev B cells - decr myeloid cells => do lymph node biopsy
107
What defines ALL?
<15 yo males Bone pain PAS stain positive TdT stain positive
108
What defines AML?
15-30 yo males Sudan stain Auer rods
109
What defines CML?
30-50 yo females t(9;22) “Philadelphia chromosome” Bcr-abl Decr LAP
110
What defines CLL?
>50 yo males w/ lymphadenopathy “Soccer ball” nuclei Smudge cells
111
What defines Hodgkin’s lymphoma?
EBV May have Reed-Sternberg cells
112
What are the B-cell Non-Hodgkin’s lymphomas?
Follicular - t(14;18) - bcl Burkitt - t(8;14) - c-myc - starry sky MP - American kids: abdominal mass - African kids: jaw mass
113
What are the T-cell Non-Hodgkin’s Lymphomas?
Mycosis fungoides - total body rash Sezary syndrome - cerebreform nuclei
114
What is polycythemia Vera?
Hct >60% Decr Erythropoietin Seen with Budd Chiari Plethoric “pruritus after bathing
115
What is essential thrombocythemia?
Very high platelets Stainable Fe Decr c-mpl
116
What are characteristics of myelofibrosis?
Megakaryocytes Fibrotic marrow => teardrop cells Extramedullary hematopoiesis
117
What are plasma cytomas?
Produce lots of Ab
118
What are manifestations of Waldenstrom macroglobulinemia?
IgM Hyperviscous
119
How does monoclonal gammopathy of undetermined significance (MGUS) present?
Old person w/ gamma spike
120
What are manifestations of multiple myeloma?
Serum M protein (IgG) Bence-Jones protein in urine Rouleaux formation Punched-out lesions
121
What is heavy chain disease?
Increased IgA Infiltration of bowel wall
122
What are manifestations of histocytosis X?
Kid w/ eczema Skull lesions Diabetes insipidus Exophthalmus
123
What does the Coombs test tell you?
Ab involved against RBC
124
What does the direct Coombs test tell you?
Ab on surface of RBCs => hemolytic anemias
125
What does the indirect Coombs test tell you?
Ab in serum
126
What is a “type and cross”?
So you know you can use that blood, and then save it for a specific patient
127
What is a “type and match”?
Type it, and then wait
128
What is forward typing?
“FABulous” Uses Ab to detect Ag
129
What is backward typing?
Uses Ag to detect Ab
130
What does blood type A tell you?
Have the A antigen
131
What does blood type O tell you?
Have no antigens Universal donor
132
What does blood type AB tell you?
Have both antigens Universal recipient
133
What does Rh+ tell you?
Has D antigen
134
What does Rh- tell you?
Does not have D antigen
135
What is Hemolytic Disease of the Newborn?
Rh neg mother Placenta tears => 100cc baby’s blood sees mom/produces Ab => attacks fetus
136
What is RHOGAM?
Anti-D IgG
137
When do you give RHOGAM?
1st dose: after delivery of 1st baby 2nd dose: week 28 of any subsequent pregnancy
138
What is the most common transplant?
Blood
139
What is a syngenic transplant?
Twin-to-twin
140
What is an autograft?
Self-to-self transplant
141
What is an allograft?
Human-to-human transplant
142
What is a xenograft?
1 species to another species
143
What is hyperacute rejection?
Within 12 hours (d/t preformed Ab)
144
What is acute rejection?
4 days to years later (d/t T-cells and macrophages)
145
What is chronic rejection?
>7 days (See fibroblasts)
146
What is graft vs. host disease?
Bone marrow transplants reject (d/t cytotoxic T cells, macrophages)
147
What are immunoprivileged sites?
No lymphatic flow => no Ag => easy to transplant (brain, cornea, thymus, testes)
148
What is INR?
Measured PT/Control PT