CIS Pales Flashcards

1
Q

definition lymphadenopathy

A

feel abnormal

painful to touch

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2
Q

what fungi can cause lymphadenopathy

A

histoplasmosis, coccidiodes

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3
Q

supraclavicular nodes drain from where

A

thorax and abdomen

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4
Q

what is panniculitis

A

inflammation of abdominal fat

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5
Q

heterophile test

A

mono

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6
Q

one very suspicious lymph node on neck

what imaging is gold standard

A

CT

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7
Q

factor VII intrinsic or extrinsic

A

intrinsic

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8
Q
14 y.o F
heavy menstruation, weakness lack concentration, Sx 7-8 mo
periods heavy and last 7-9 days
easy bruising, bleed after tooth extraction age 7
normal vital signs
WN/WD, pale, no bruises
Hb 9.5 MCV 69
ddx?
A

Fe deficiency anemia

bleed disorder- vwD, hemophilia

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9
Q
14 y.o F
heavy menstruation, weakness lack concentration, Sx 7-8 mo
periods heavy and last 7-9 days
easy bruising, bleed after tooth extraction age 7
normal vital signs
WN/WD, pale, no bruises
Hb 9.5 MCV 69
Labs to order?
A
CBC
PT
PTT
platelet count
PS
Iron panel
PFA platelet function analyzer
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10
Q
14 y.o F
heavy menstruation, weakness lack concentration, Sx 7-8 mo
periods heavy and last 7-9 days
easy bruising, bleed after tooth extraction age 7
normal vital signs
WN/WD, pale, no bruises
Hb 9.5 MCV 69
normal PTT PT platelet count
elevated bleeding time, elevated PFA
A

not problems in coagulation cascade

qualitative problem with platelets

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11
Q

medicaitons that can cause qualitative problems with platelets

A

aspirin, NSAIDs

clopidogrel, abcixumab (IIa/IIIB inhibitor)

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12
Q

What is type 2N vwD

A

normal levels vWF, RIPA and multimer pattern

low factor VIII (prolongs PTT)

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13
Q

how will low VIII change PT PTT

A

prolonged PTT

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14
Q

20 mo boy with Hx joint swelling and bruising
deep hematomas in thigh mm, not walking on own
no Hx bleeding problems in parents, or 3 siblings
pale wd/wn
tenderness around ankles dec ROM b/l
no petechial rashes
ddx?

A

hemophilia
ITP
single factor deficiency

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15
Q

what do you have to check with rashes

A

blanching or not?

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16
Q

20 mo boy with Hx joint swelling and bruising
deep hematomas in thigh mm, not walking on own
no Hx bleeding problems in parents, or 3 siblings
pale wd/wn
tenderness around ankles dec ROM b/l
no petechial rashes
tests to order?

A
platelet count
bleedting time
PT
PTT
PFA
CBC
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17
Q

20 mo Hx hematomas
elevated PTT normal PT
ddx?

A
inherited deficiency VIII, IX, XI
deficiency facotr XII
vwD
acquired: heparin, inhibitor VIII, IX XI XII
acquired vwD
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18
Q

normal PTT long PT

ddx?

A

inherited factor VII deficiency

acquired: factor VII def, vit K def, liver disease, coumadin/warfarin, inhibitor factor VII

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19
Q

prolonged PT and PTT

ddx?

A

liver disease
DIC!!!
heparin and warfarin
inherited: combined def, def prothrombin etc…

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20
Q

how can you differentiate between factor deficiency and factor inhibitor problems?

A

mixing study: mix plasma with normal plasma
if corrects PTT then was deficiency
if does not correct there is an inhibitor

21
Q

factor VII shows deficiency and when mixed with normal plasma PTT was corrected
what 2 diseases need to check for

A

Hemophilia A

vwD

22
Q

boy with hemophilia, what family Hx do you look into

A

males on mothers side

23
Q

bleeding in minor cuts more likely platelets or hemophilia?

24
Q

large subcutaneous soft tissue hematomas more likely in hemophilia or platelet deficiency

A

hemophilia

25
Pt PTT and BT for DIC
long BT, long PT long PTT
26
55 y.o F Hx HTN and RA on lisinopril, aspirin, methotrexate and ibuprofen no Hx easy bruising or bleeding WBC7.5, Hb 11.1 MCV98, platelets 84 (low) repeated platelets 85 why no Sx?
Sx start between 10 and 20k
27
first thing to do when see asymptomatic patient with thrombocytopenia
redo it | could have pseudothrombocytpenia (clumping from EDTA)
28
platelet levels needed for minor surgery? major?
minor >80 | major >100
29
What can cause thrombocytopenia from decreased production
viral infecito, chemo alcohol BM aplasia Vit B12/folate deficiency
30
what can cause thrombocytopenia from increased destruction
``` ITP, autoimmune, viral infection, drugs, MAHA= DIC, TTP, HUS HELLP syndrome (pregnancy) ```
31
what are weird causes of thrombocytopenia
dilution (after big transfusion) | splenic sequestration
32
what do you want to known in patient with low platelets but asymptomatic some macrocytic cells
viral infection nutrition recent Hx hospitalization requiring DVT prophylaxis
33
tests to order for asymptomatic thrombocytopenic patient
``` PS to look for schistocytes PT PTT Fibrinogen BM biopsy HIV ```
34
alcohol can cause what in blood
thrombocytopenia by suppressing bone marrow and increase splenic sequestration
35
PS normal, PT normal, PTT normal, fibrinogen normal, BM biopsy normal in asymptomatic thrombocytopenic patient most likley?
Ab to platelets | ITP
36
DIC labs
PT PTT fibrinogen levels!!!
37
fibrinogen(II) levels in DIC
decreased because used up
38
what are confirmatory tests for ITP
Dx by exclusion
39
Tx ITP
steroids and splenectomy
40
59 y.o M alcoholism, severe pneumonia, intubated and got a rash, melena high WBC, Hb8.1 platelets 17 (LOW) PTT 71 PT 21 (both high) on antibiotics, pantoprazole(PPI) prophylaxis enoxaparin for DVT, DT, delerium tremons prophylaxis diazepam ddx?
``` HIT liver cirrhosis/liver disease alcohol related BM suppression infection splenic sequestration DIC ```
41
59 y.o M alcoholism, severe pneumonia, intubated and got a rash, melena high WBC, Hb8.1 platelets 17 (LOW) PTT 71 PT 21 (both high) on antibiotics, pantoprazole(PPI) prophylaxis enoxaparin for DVT, DT, delerium tremons prophylaxis diazepam tests to order?
``` liver enzymes fibrinogen retic count free plasma Hb U/s spleen PS haptoglobin ```
42
normal coagulation studies with non-blanching rash
vasculitis until proven otherwise
43
C-ANCA elevated | biopsy shows leukocytoclastic vasculitis
wegeners GN
44
26 y.o F ER with SOB hemoptysis and painfully swollen left leg, no previous medical or surgical Hx, takes Yaz, MVI, parents and siblings healthy, CBC and CMP normal labs?
PT PTT U/S leg CXR V/Q scan CT
45
after labs F with swollen leg and SOB has DVT found on U/s and V/Q mismatch showing PE CT scan shadow in pulmonary artery, clot in L side causes?
genetic predisposition- factor V leiden, protein C or S deficiency, antithrombin III def, antiphospholipid Ab virchows triad procoagulant drugs: birth control pills
46
what are primary hypercoagulable states
deficiencies of antithrombotic factors: antithrombin III, protein C or S excess of prothrombotic factors: factor V leiden and prothrombin mutation
47
what are secondary causes of hypercoagulable states
cancer, pregnancy, BCP anti-phospholipid syndrome trauma, surgery and immobilization
48
what disorders predispose to arterial AND venous clots
``` antiphospholipid syndrome (SLE) hyperhomocysteine ```
49
clotting tx duration if not genetic
3-6 mo