UA final review Q's 2 Flashcards

1
Q

10 mo. old is pale and listless upon physical examination, chiro ordered a CBC, platelet count, total serum iron and ferritin study. results are: HCT=24 & MCV=68.6
microscopic reveals significant anisocytosis, microcytosis, hypochromia, and piokilocytosis. a normal distribution of platelets was present. stool and urine studies are negative for blood or parasites. what category of anemia is suggested by the morphology of the RBC’s and blood results.

A

iron deficiency

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2
Q

what other signs on inspection would aid you in ur dx?

A

-swelling of the tongue
-dry lips
-craving for ice chips
(all the above)

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3
Q

the second leading cause of anemia worldwide is

A

chronic disease

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4
Q

the infectious microorganism directly associated with hemolytic uremic syndrome is

A

E-coli 157-07

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5
Q

a risk factor for vitamin B-12 anemia is:

A

vegetarian diet

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6
Q

a pt. presents with abdominal distress, neurological disturbances and trouble seeing yellow and blue. you would order:

A

vit B-12 study

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7
Q

which of the following is not associated with hemolytic anemia

A

increased haptoglobin

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8
Q

john presents in ur office with dyspnea, jt. pain and fatigue. he is a 25 yoa black male who has experienced these symptoms on and off for several years. the crisis seem to come and go. what factors contribute to the erythrocyte disorder you suspect in this pt.?

A

sickling is spontaneous

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9
Q

which of the following dx tests would provide aid in conformation of your suspicions? (john)

A

-CBC
-UA
-microscopic blood analysis
(all the above)

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10
Q

what is the condition u would suspect?

A

sickle cell

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11
Q

john’s prob. can be corrected by?

A

cannot be corrected bc its genetic in nature

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12
Q

with iron deficiency anemia, u would suspect?

A

low MCV low hematite and low MCHC

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13
Q

which of the following anemias are megaloblastic?

A
  • B12 deficiency

- & folate deficiency

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14
Q

cobalamin transport out of the gut is mediated by:

A

intrinsic factor

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15
Q

aplastic anemia can be caused by:

A

-infection
-EBV
-radiation
(all the above)

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16
Q

pts. with aplastic anemia need to be identified quickly as it will progress quickly and result in death. T/F?

A

true

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17
Q

in a pt. with hereditary spherocytosis you would expect to ind this on palpation of the abdomen:

A

enlarged spleen

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18
Q

in sickle cell anemia the pt. possesses an abnormal form of hemoglobin called:

A

hemoglobin S

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19
Q

u receive a lab report on a pt. and u notice the number of WBC is 450,000. u would suspect?

A

leukemia

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20
Q

polycythemia may be due to :

A

decreased plasma

21
Q

polycythemia may also be due to:

A

increase in number of cells

22
Q

the mild form of thallasemia responds to:

A

no treatment

23
Q

a pt. present with high fever, sore throat and achy muscles. she is a 22 yoa female. her blood work is: WBC differential, neutrophil-28%, lympo.-68%, mono.-2%, eosin.-2%, & baso.-1%. wat do u suspect is her problem?

A

viral infection

24
Q

if she reported a new boyfriend w/ similar symptoms you would suspect

A

mononucleosis

25
if she had positive streptococcus culture or ASO, you wold now suspect:
strept throat
26
what would u expect to find on the clinical exam of this pt.?
spleenomegally
27
joe is an italian american. is is overweight and reports poor dietary habits. he has fatigue and pallor. he is 40 yoa, and has had mild symptoms like this on and off his whole life. his disease would be characterized by:
absence or decrease in synthesis of one or more goblin subunits
28
vito spatfore has a fasting lipid profile of 300 (normal
LDL 250 HDL 50
29
if you saw hair on end appearance on a cervical X-ray, you would suspect?
thallasemia
30
which of the following anemias are microcytic?
-iron deficiency -chronic disease anemia -thallasemia (all of the above)
31
ESR is __, but not __.
Sensitive/specific
32
an iron deficiency anemia, the erythrocyte indices are typically:
MCV decreased, MCH decreased
33
what is the most common cause of iron deficiency anemia?
loss of nutrient exceeding the replenishment of nutrient
34
what is the combination which may result in erythroblastosis fetalis anemia?
Rh (+)father, Rh (-) mother, Rh (+) baby
35
what is the normal response to living at high altitudes, in a lowered oxygenated environment?
physiologic polycythemia
36
what does MCV tell u?
average size of the red blood cell
37
what lab test would give information about a pt's electrolyte/hydration status?
complete metabolic panel
38
hemophilia is a lack of __ and its severity is dependent on __.
factor VIII/ the severs of the genetic disorder
39
bruising without a cause usually would most likely be classified as:
thrombocytopenia
40
erythrocytes:
-are anucleated -outnumber the WBC -are dependent on structure (all of the above)
41
if you see a pt with 400,00- platelets per ccm you would suspect:
a normal patient
42
a platelet count of 50,000 will put the pt at risk for
spontaneous bleeding
43
von willabrands disease is a problem w/
platelet adhesion
44
a pt. with a sever deficiency of vit. K would be at risk for?
spontaneous bleeding
45
glucose:
60-100 mg/dl
46
sodium:
135-147 mEq/l
47
calcium:
8.8-10.3 mEq/l
48
chloride:
95-107 mEq/dl
49
potassium:
3.5-5.2 mEq/dl