Hematology l Flashcards

1
Q

what is TIBC
if high
if low

A

% transferrin saturation; total iron binding capacity
high - iron xu anemia, pregN
low - anemia of chronic dz, sideroblastic anemia, hemochromatosis

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2
Q

ferritin elevates during when

A

inflamma and cancer

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3
Q

right shift can be due to

A

b12 olae xu, hypersegmentation of neutrophils

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4
Q

MCV low =

A

iron xu, thalassemia, lead poisoning

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5
Q

microcytic hypochromic anemia dt

A

iron xu, severe protein xu, thal, chroic infx

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6
Q

normocytic normochronic anemia dt

A

loss of blood or loss of blood production

- then look at reticulocytes

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7
Q

Hemochromatosis is usu dx at what age?

complications

A

middle aged

LR failure, pancreatic failure

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8
Q

Henoch Schonlein purpura
age
presentation

A

children < 10 yo
usu acute URI precedes it
IgA in small vessels and joints
1. RASH 2. ABD PAIN OR RENAL 3. ARTHRITIS … see bruising on areas of pressure like buttocks

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9
Q

thrombotic thrombocytopenic purpura, TTP

presentation

A

FATAL DIE AT 40yo
vWF cleaving protease inhibited
clotting in small vessels so decrease in plt

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10
Q

Dx TTP

A

microangiopathic hemolytic anemia
schistocytes, helmet cells
increase LDH
mental status or focal neuro deficits

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11
Q

Hemolytic Uremic Syndrome

presentation

A

toxin, bacteria or drug causes hemolytic anemia —> blocking fxn of KD so failure there and build up of UREMIC acid

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12
Q

von Willebrand Dz

A

labs normal, so have to do clotting studies

either see light to heavy bleeding depending on genetics - many never diagnosed

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13
Q

DIC

A

usu ACUTE like complications obstetrics, infxn, malign - when all clotting factors are used up

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14
Q

Hemophilia A vs B

A

x-linked recessive
A = 8 factor
B = 9 factor; peds, dx factor 9 assay, tx FFP

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15
Q

Polycythemia vera vs Reactive Polycthemia

A

PVera - is true, ITCHY AFTER BATH, easy bruising bleeding; high RBC

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16
Q

MC ETIC OF Reactive POLYCYTHEMIA

A

emphysema dt increase in erythropoietin

other eti: renal, tumor, tetralogy of fallot

17
Q

Leukemia vs Lymphoma

A

leukemia - SP & LR enlarged

lymphoma - LA

18
Q

Multiple Myeloma
age
presentation

A

> 50 yo
IgG or IgA is jumbled in attacking a neoplastic plasma cell
SSx: bone back pain, fractures, bleeding agg of arrhythmias
BENCE JONES PROTEINURIA
PUNCHED OUT BONE LESIONS

19
Q

BENCE JONES PROTEINURIA

A

MM, Waldenstrom’s Macroglobulinemia

20
Q

PUNCHED OUT BONE LESIONS

A

MM

21
Q

Waldenstroms Macroglobulinemia

A

> 50 yo, B lymphocytes & IgM

22
Q

Types of Leukemias, age, prognosis

A

ALL - mc in children, F, bone pain, hepatosplenomegaly, 90% cure
AML - older children 15-39 yo, worse progN, splenomegaly
CML - 45 yo, any cell affected, chronic, remit and relapse, PHILADELPHIA CHROMOSOMES
CLL - > 55 yo, no sxs at first, see super high WBC 50-250,000, progn good

23
Q

AUER RODS

A

AML

24
Q

PHILADELPHIA CHROMOSOMES

A

CML

25
Q

Single node that spreads

A

Hodgkin’s lymphoma

26
Q

Hodgkin’s lymphoma

A

single node that spreads

intermittent spiking F

27
Q

Non-Hodg vs Hodg - which worse?

A

Non-Hodg - no age limits too

28
Q

Burkitt’s Lymphoma
presentation
complications

A

B-lymphocytes
LA in maxilla or mandible
can lead to Non-Hodgkins