Case 3: Breaking Bad Flashcards

1
Q

What is a bruise?

A

broken capillaries

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are our circadian rhythms regulated by?

A

body clock, clock genes, environment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Hoe can flight fatigue be treated?

A

melatonin pills, light therapy, going by destination times

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is serotonin converted to?

A

melatonin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is melatonin production inhibited by? What does it do?

A

production inhibited by light
inhibits circadian alerting system
drowsiness and lowers body temp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the three components of blood?

A

plasma
buffy coat
RBC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are three granulocytes? Where are they found and what type of nucleus do they have? What do they do?

A

neutrophils
eosinophils
basophils

cytoplasm

polymorphic

phagocytose bad things

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Where do agranulocytes originate? What are four of their names and what do each do?

A

bone marrow

lymphocytes
T cells: mature in thymus, circulate and attack viruses
B cells: mature in marrow, produce antibodies to circulate
monocytes: can develop into dendritic cells and phagocytose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What 3 agranulocytes are considered natural killer cells?

A

lymphocytes, T cells, B cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are platelets derived from?

A

ruptured megakaryocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the four steps of coagulation of mature thrombus?

A
  1. injury
  2. platelets form primary haemostatic plug (soluble)
  3. recruitment of more platelets
  4. coagulation factors and thrombin = second haemostatis and fibrin clot (insoluble)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What does low platelet number indicate?

A

bone marrow/megakaryocyte disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What does low RBC and haemoglobin indicate?

A

anaemia

bone marrow disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What does low leukocytes indicate?

A

more likely to get infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What does high Ca2+ indicate?

A

abnormal break down of bone

bone metabolism disorders

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What 4 body systems maintain calcium homeostasis?

A

skeletal
GIT
endocrine
renal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is high levels of calcium in the blood called and what are the symptoms?

A

hypercalcemia

decreased appetite, nausea, frequent urination, kidney stones

18
Q

What are the 3 functions of the skeletal system?

A

mineral homeostasis
haematopoiesis
energy storage

19
Q

What two substances are bones made out of?

A

collagen type 1

calcium crystalline hydroxypatite

20
Q

Where is the periosteum located?

A

on the outside of the bone

21
Q

Where is the endosteum located?

A

lines the medullary cavity

22
Q

What are the four stages of bone remodeling?

A

resorption
reversal
formation
mineralization

23
Q

How does aspirin inhibit bone growth?

A

interferes with collagen

24
Q

How can bone health be tested? (2)

A

bone mineral density test
DXA test (T-score measured in standard deviations)
-4 to -1 unhealthy, -1 to +2 healthy

25
Q

What are multiple lytic lesions?

A

oil droplet like formations where bone has weakened

26
Q

How long after birth does haematopoiesis occur in the bone marrow?

A

by 10-12 weeks

27
Q

What is the bone marrow distribution like at birth (red/yellow)?

A

all red

28
Q

How can the cellular constitution of marrow be assessed?

A

biopsy of hipbone/posterior iliac crest

complete blood count test

29
Q

What do plasma cells develop from? What do they produce?

A

B cells that originate in bone marrow

produce immunoglobins

30
Q

How many chains are immunoglobins made up of and why is this important?

A

4 chains

dictate what antigen they attack

31
Q

What is a paraprotein? What can it be detected by?

A

malignant plasma produce a single non-functional immunoglobin in large quantities (paraprotein)
Serum protein electrophoresis

32
Q

What is the Bence-Jones protein? What cases are they present in?

A

abnormal plasma protein which also produce free immunoglobin light chains (filtered by kidneys)
present in 2/3 multiple myeloma cases

33
Q

What are the features of multiple myeloma?

A
bone destruction and pain
immunosuppression
hypercalcemia
bleeding/bruising
renal failure (light chains trapped in tubules)
34
Q

How can multiple myeloma be diagnosed?

A

SPEP
urine electrophoresis
bone marrow biopsy
x-ray

35
Q

What are the five clinical phases of multiple myeloma?

A
post germinal centre B cell
MGUS
smouldering myeloma
myeloma
plasma cell leukemia
36
Q

What is MGUS characterized by? (4)

A

benign
less than 10% plasmacytosis
paraprotein
no “CRAB”

37
Q

What is smouldering myeloma characterized by? (3)

A

equal to or more than 10% plasmacytosis
increased paraprotein
no “CRAB”

38
Q

What is myeloma stage characterized by? (5)

A
more than 10% plasmacytosis
increased paraprotein
"CRAB"
staged I-III 
treatment begins
39
Q

What are the “CRAB” symptoms?

A

calcium elevation
renal failure
anemia
bone pain

40
Q

What is the prognosis of myeloma determined by?

A
clinical phase
age
"crab" symptoms
response to initial treatment
prognostic chromosomal changes
41
Q

How is myeloma treated? (12)

A
hydration
correction of hypercalcemia
pain relief
radiotherapy
transfusion
treatment of infection
surgery
vaccination
chemotherapy
targeted drugs
high dose radiation therapy (+ injections of stem cells)
novel agents (stop growth and kill)