GI/Hematology Flashcards

1
Q
A

All three

1 - px can be taking NSAIDs to treat pain

2 - H.pylori is possible

  1. Steroids can cause ulcers
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2
Q

Patient takes 800mg Ibuprofen daily. Which of the following is true:

  1. By inhibiting cyclooxegenase, NSAIDs can increase the risk of gastric ulcers
  2. He should stop ibuprofen
  3. He should begin a proton pump inhibitor
A

1 , 2, 3

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3
Q
A

none are correct

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4
Q

Inflammatory bowel disease vs Irritable bowel syndrome

A
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5
Q
A

VITAMINS ARE PRIMARILY ABSORBED IN SMALL INTESTINE

B

C

(Not ulcerative colitis- inflammation only in colon)

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6
Q
A

A

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7
Q
A

D

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8
Q
A

C , D

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9
Q

Bilateral episcleritis with ulcerative colitis

A
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10
Q

Erythropoiesis (Red blood cell life cycle)

A
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11
Q

CBC (complete blood count)

A
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12
Q

Complete blood count

Hemoglobin/hematocrit

A

Hemoglobin (HGB)

  • Concentration of hemoglobin (oxygen carrying molecule) in a concentration of whole blood (g/dl)
  • Low O2 = hypochromic (pink colour)
  • Normal O2 = normochromic (red)
  • High O2 = Hyperchromic (dark red)
  • Small size = microcytic
  • Normal = normocytic
  • Large = macrocytic

Hematocrit

  • Packed spun volume of blood that contains intact RBCs (%)
  • Measured followind centrifugation

Low= anemia

High = polycythemia

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13
Q

Bone marrow dyscrasia (disorder) - RBC

A
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14
Q
A

D

(Can have normal iron levels in Anemia- only used to classify anemia)

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15
Q
A

A

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16
Q

Healthy 30 year old woman is found to have anemia. Well nurished, unremarkable medical history. Iron most likely deficient.

Select most appropriate next step in evaluation:

  1. Evaluation to rule out colon cancer
  2. Testing of B12 levels to rule out B12 as cause of anemia
  3. Treat with iron to see is blood count responds
  4. Work up to exclude sickle cell disease
A

3

(1 probable in older individual)

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17
Q
A

A , B

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18
Q
A

Abnormal white blood cells

Large red blood cells (high MCV)

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19
Q

30 year old female presents with anemia

A

A

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20
Q

30year old female.

A

A, B, E

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21
Q

30 year old female

A

A, B, C

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22
Q

Other measures of iron

Transferrin/total iron binding capacity (TIBC)

Ferritin

A
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23
Q
A

A

(C- first check for colon cancer)

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24
Q
A

C

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25
E - all
26
Proliferative Sickle Retinopathy
27
A, C (b- increases production of RBC in marrow) (Reticulocytes - immature RBC)
28
D (B12 causes macrocytic anemia, pernicious anemia)
29
All options
30
Leukocytes - WBC
31
Leukocyte disorders
32
Leukemia
33
Lymphoma
Reed-sternberg cells only in Hodgkins lymphoma Only in lymphoid line
34
Leukemia or lymphoma Are cancer cells circulating
35
Eye findings in leukemia and lymphoma
36
A, B, D
37
B
38
D- all
39
26 male with no significant medical history, has reduced vision in OS for a month Saw ER 3 weeks ago with complaint of easy bruising-"could be explained by mild trauma", ER did not check CBC Returned to ER 2 weeks later with same complaint in addition to blurry vision OS In eye clinic patiets admitted to fatigue/malaise; eye dr noticed pale skin
Retinopathy in blood dyscrasia * Retinal hemorrhaging is related to anemia, thrombocytopenia and increased venous pressure( in hypercoagulable states) * Hemes more common with anemia AND thrombocytopenia than either alone (Hgb \<8 , PLT\<50) * Tyoically need Hct \<= 50% of normal to get CWS/bleeding due to anemia alone You need SEVERE or VERY SEVERE anemia to have retinal findings(worse if concurrent thrombocytopenia) * Cotton wool spots are signs of retinal ischemia * Obstruction of axoplasmic transport = formation of "cytoid bodies" on histology * RNFL is thickest around the nerve - often see CWS here * Roth spots are nonspecific white-centered hemorrhages * Clasiccaly described in leukemia + endocarditis * Ischemic RNFL vs fibrin/PLT vs infectious material vs neoplastic cells
40
A Reed-sternberg cells only in Hodgkins
41
All of the above
42
Leukocyte disorders - Immunoglobulin disorders
43
Retinopathy in hyperviscosity and clotting disorders
44
A, B, C
45
A, B, C
46
47
Definition of thrombocytopenia
Decreased platelets, Less clotting, more bleeding Causes: bone marrow failure, Ab-mediated destruction, drugs * Thrombotic thrombocytopenic purpura * Idiopathic thrombocytopenic purpura ("-penia" - blood cell deficiency)
48
Thrombocytosis
Too much platelets, increased chance of clotting Causes: Inflammation (physiologic) ("-cytosis" or "-philia" - blood cell excess)
49
Does aspirin cause reversible or irreversible inhibition of platelets?
Irreversible | (NSAIDs are reversible)
50
Coagulation disorders Protein C deficiency
Congenital/acquired condition that leads to increased risk for thrombosis Causes of aquired deficiency include: * Acute thrombosis * Warfarin therapy * Liver disease * Vitamin K deficiency * Sepsis * Disseminated intravascular coagulation * Certain chemotherapeutics * Uremia
51
Coagulation disorders Factor V Leiden Mutation
Caused by mutaions in F5 gene
52
Hemochromatosis
Genetic predisposition to abnormal iron absorption = plebotomy necessary Risk for organ damage
53
Coagulation disorders
54
Only A (B- irreversably inhibits) (C-genetic imparement|)
55
B, D | (von willebrands causes more bleeding)
56
A, B, D px has hemochromatosis
57
B, D
58
Irritable bowel disease
59
60 yo white female Noticed blurry vision for 2months since hitting her head. Right eye gradually improved, left remains poor Hypertension (lisinopril) BCVA with correction * OD: 20/125 * OS: 20/40 IOP: OD: 13 ; OS: 14 SLE: anterior segment unremarkable, 1+ NS OU; no AC cells; no vitreous cells BP 129/66 A1c: 5.8 WBC 354 (leukocytosis) (normal: 3.7-10.5) RBC 2.37 (normal:4-5.2) Hb 7.3 (normal: 11.9-15) hct: 22 (normal:35-45) (anemia) Plt: 81 (normal:150-400) (Thrombocytopenia)
Diagnosis: Leukemia
60