Exam 1 Week 1 Flashcards

1
Q

5 Types of WBC’s and precursors

A

Lymphocytes (lymphoid, B and T cells) Neutrophils (myeloid) Monocytes (myeloid) Eosinophils (myeloid) Basophils (myeloid)

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2
Q

Leukemia vs. lymphoma

A

Leukemia: arise from bone marrow, in blood Lymphoma: arise from lymph system, in lymph

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3
Q

Serum vs. plasma

A

Serum: blood without the clotting factors (post-clot) Plasma: blood without RBC, WBC, and platelets

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4
Q

Red part of CBC

A

Hemoglobin, Hematocrit, RBC count MCV, MCH, MCHC Platelet count, mean platelet volume Red cell distribution width (CV and SD) NRBC Percent, NRBC Absolute

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5
Q

White part of CBC

A

WBC count Segmented neutrophil % and abs Lymphocyte % and abs Monocyte % and abs Eosinophil % and abs Basophil % and abs

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6
Q

MCV MCH MCHC Red cell distribution width

A

MCV - average volume of RBC’s MCH - content (weight) of hemoglobin in average RBC MCHC - average concentration of hemoglobin in RBC vol RCW - variation of size of RBCs (histogram)

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7
Q

Calculate: MCV MCH MCHC

A

MCV = Hct/RBC x 10 (tallest peak on RCW histogram) MCH = Hgb/RBC x 10 MCHC = Hgb/Hct x 100

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8
Q

CBC lab techniques

A

Impedance (Coulter Principle) Light scattering techniques Flow cytometry/cytochemistry Platelet counting can be complicated by clumping

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9
Q

Scattergrams

A

Forward scatter: size Side florescent: type and quantity of nuc acids/organelles Side scatter: internal cell information Basophils/lymphocytes will be same scatter Basophils resistant to acid cyto stripping

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10
Q

Limitations of reference intervals

A

Based on patient populations 2 SD (p=.05) Normal can be abnormal and vice versa

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11
Q

CBC Differential

A

Automatic vs. manual (requested or flagged) 1. Make blood film 2. Examine at low power for obvious morphologic 3. Examine at high power for detail

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12
Q

RBC and Platelets on peripheral smear

A

RBC - little variation Platelets - small/fine granules, often clumped

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13
Q

WBC on peripheral smear

A

Neutrophils: distinct lobes, granules Lymphocytes: smaller, scant cyto with round nuc Monocytes: largest, irregular/lobed, vaculoes Eosinophils: bi-lobed, larger granules (red/orange) Basophils: large purple/black granules (obscure nuc)

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14
Q

PRR TLR PAMP DAMP

A

PRR: pattern-recognition receptor, on body cell TLR: toll-like receptor, subtype of PRR, ~10 PAMP: pathogen pattern, on foreign cell DAMP: damage pattern, on body cell

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15
Q

Most common/TLR final transcription factor

A

NF-kB

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16
Q

4+1 hallmarks of inflammation

A
  1. rubor (erythremia) 2. calor (warmness) 3. tumor (swelling) 4. dolor (pain) +1. Loss of function
17
Q

Dendritic cells

A

aka. antigen presenting cell Bridge between innate and adaptive immunity Located in skin, lung, mucus mmbr etc Immature DC take anything they can and travel

18
Q

6 Types of Immunopathology

A

Type I: immediate hypersensitivity, IgE, allergies Type II: autoimmunity Type III: antibodies against soluble antigen, tissue injury Type IV: T-cell mediated, bystander injury Chronic, frustrated immune response HIV/AIDS

19
Q

Anemia Flow Chart

A

Associated with other hematologic abnormalities? Appropriate reticulocyte response? What are red blood cell indices?

20
Q

Labs tests for anemia

A

CBC Wright’s stain to look at morphology Reticulocyte count (rate of production)

21
Q

Reticulocyte count

A

RC = % of 1000 RBC’s (0.4-1.7%) mRNA presence in RBC’s 3 days in marrow, 1 day in blood Marker of RBC production

22
Q

Absolute reticulocyte count

A

ARC = % RC x RBC count Determines relevance of RC >50,000/ul is high

23
Q

Reticulocyte index

A

RI = RC x (patient hgb/normal hgb) x (1/sf) Corrects for stress 1.0-2.0 2 = increased destruction

24
Q

Iron storage

A

Hemoglobin 65% Myoglobin 6% Herritin/hemosiderin (plasma) 25% Transferrin/ferroportin Enzymes

25
Q

Intralumenal factors for iron absorption

A

presence of amino acids (up) presence of vit c (up) more iron (up) phytates, oxalates, iron precipitates (down) less iron (down)

26
Q

Extralumenal factors for iron absorption

A

increased RBC creation (even if excess iron)

27
Q

Iron Cycle

A

Transferrin: made in liver, binds 2 ferric iron, receptor

RE Cycle: macrophage breakdown, ferritin store

Ferritin = hemosiderin, stores 4500 Fe

Hepcidin: negative regulator of Fe absorption

28
Q

Timeline of Iron Deficiency

A

Normal

Iron Deficiency

Iron Deficient Erythropoiesis

Iron Deficiency Anemia

29
Q

Iron Deficiency Anemia Lab Findings

A

Decreased Hgb, Hct, RC, RI

Later: decreased MCV, increased RDW

Elliptocytes, spherocytes, fragemented RBC, target cells

30
Q

Iron Overload Etiologies

A

Increased iron in diet

Increase iron absorption (HFE mutation, hemochromatosis)

Repeated transfusions (hemosiderosis)

31
Q

Iron Overload Effects and Treatment

A

Heart, liver, endocrine (pancreas) damage

Hemochromatosis = therapeutic phlebotomy

Hemosiderosis = iron chelators (desferal, exjade)