Uworld7 Flashcards

(101 cards)

1
Q

spherocytes w/o central pallor, found when?

A

Autoimmune hemolytic anemia

Hereditary spherocytosis

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2
Q

Side effect of cyclosporine

A

gout

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3
Q

side affect of amiodarone and lithium

A

thyroid dysfunction

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4
Q

Blood transfusion anaphylactic reaction

- w/in seconds to minutes 
- Angioedema, hypotension, difficulty breathing
A

IgA Deficiency

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5
Q

blood transfusion - life threatening
within 1 hour of transfusion
fever, flank pain, hemolysis, oliguric renal failure, DIC

A

ABO mismatch

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6
Q

what reduces the risk of febrile non-hemolytic transfusion

A

Leukoreduction of donor blood

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7
Q

What reduces the risk of IgA deficiency

A

washed

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8
Q

clinical features and timing of febrile nonhemolytic transfusions

A

within 1-6 hours

fever, chills, and malaise without hemolysis

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9
Q

bone cancer: soap bubble appearance and most likely location

A

giant cell tumor

distal femur and proximal tibia around the knee

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10
Q

bone cancer: pain worse at night and unrelated to activity and quickly relieved with NSAIDs

A

osteoid osteoma

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11
Q

bone cancer: commonly due to hyperPTH from parathyroid carcinoma

A

osteitis fibrosa cystica

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12
Q

treatment for cancer anorexia

A

progesterone analogues and corticosteroids

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13
Q

Salvage therapy

A

treatment for a disease when standard therapy fails

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14
Q

Neoadjuvant therapy

A

treatment given before the standard therapy for a particular disease

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15
Q

Maintenance therapy

A

given after induction and consolidation therapies to kill any residual tumor cells and keep the patient in remission

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16
Q

Induction therapy

A

initial dose of treatment to rapdily kill tumor cells and send the patient into remission

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17
Q

Consolidation therapy

A

given after induction therapy with multidrug regiments to further reduce tumor burden

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18
Q

Adjuvant therapy

A

treatment given in addition to standard therapy

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19
Q

Salvage thearpy

A

treatment for a disease when standard therapy fails

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20
Q

Most common cause of inadequate response to erythropoiesis-stimulating agents for CKD

A

iron deficiency

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21
Q

risk factor for taking erythropoietin

A

hypertension
headache
retinal hemorrhages
NOT cerebral venous thrombosis

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22
Q

unique clinical presentation for CLL

A

hepatosplenomegaly

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23
Q

Monoclonal abs against CD20

A

rituximab

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24
Q

Inhibits BCR-ABL tyrosine kinase

A

Imatinib

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25
Periphearl smear for CLL
lymphocytosis (smudge cells)
26
Teardrop-shaped red blood cells
beta thalassemia or myelofibrosis
27
Treatment for EHEC
avoid abs
28
When do you do urological imaging for acute pyelonephritis
48-72 hours later despite treatment
29
Treatment for uncomplicated and complicated acute pyelonephritis
fluoroquinolones
30
treatment for animal and human bit injuries
amoxicillin-clavulanate
31
When do you see Procalcitonin
after bacterial pneumonia
32
difference between Ehrlichoiosis and Babesiosis
Ehrilichosis: leukopenia and thrombocytopenia Babesiosis: thrombocytopenia
33
What is leukoctye alkaline phosphatase levels?
low in CML
34
lab value for CML
leukocytosis | increased basophil
35
how is G6PD deficiency inherited
X-linked recessive disorder
36
Peripheral smear for G6PD deficiency
Heinz ( red blood cell inclusions seen after crystal violet staining) bite cells
37
Peripheral smear for ALL
lymphoblast
38
during heparin induced thrombocytopenia when can warfarin be initiated
greater than 150,000 platelet count
39
What is gold standard confirmatory test for HIT
serotonin release assay
40
What defines HIT
1. thrombocytopenia 2. thrombosis (arterial or venous) 3. 50 or more percent drop platelet baseline 5-10 days after initiation
41
Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangectasia)
Diffuse telangiectasia (oral lesions) recurrent epitstaxis widespread AV malformations (pulmonary AV- hemoptysis)
42
How is hereditoary spherocytosis inherited
autosomal dominant
43
Triad for hereditary spherocytosis
hemolytic anemia jaundice splenomegaly
44
Hereditory spherocytosis has increased osmotic fragliity on what
acidified glycerol lysis test
45
what abnormal binding test is positive for herediatory spherocytosis
eosin-5-maleimide binding test
46
Pyridoxine
Vitamin B6
47
role of pyridoxine and homocytseine
B6 lowers homocystine
48
blood transfusions may elevate levels of what in the blood
citrate, then chelates calcium and magnesium
49
clinical picture for factor V Leiden
increased risk of thrombosis
50
pathophys for factor V Leiden
Activated protein C resistance
51
treatment for immune thrombocyotpenia in children
IVIG or steroids
52
Treatment for immune thrombocytopenia in adults
more than 30,000: observe | less than 30,000: IVIG or steroids
53
What is anithrombin associated with
DIC cirrhosis nephrotic syndrome
54
diferential diagnosis for microcytic/hypochromic anemia
iron deficiency anemia of chronic disease thalassemia lead poisoning, siderblastic anemia
55
Iron and ferritin levels for thalassemia
high
56
how is leukamoid reaction different from CML
leukocyte alkaline phosphatase elevated in Leukamoid | No basophils in leukamoid
57
bone marrow shows clonal plasma cell proliferation
multiple myeloma
58
bone marrow shows hypocellular and fibrotic bone marrow
myelofibrotic disorder
59
difference between bone scans and skeletal survey
bone scans: osteoblastic, metastatic solid tumors | skeletal survey: osteolytic
60
what is a risk factor for Meylodysplastic syndrome
previous chemotherapy/radiation
61
What is the difference between B12 deficiency and myelodysplastic syndrome on peripheral smear
MS: hyposegmented neutrophils B12: hypersegmented neutrophils
62
Trousseau's syndrome? what is it associated with it
hypercoagulability disorder recurrent and migratory superficial thrombophlebitits pancreatic cancer or stomach, lung prostate
63
What will flow cytometry show for paroxysmal nocturnal hemoglobinuria
absence CD 55 and CD59
64
clinical picture for paroxysmal nocturnal hemoglobinuria
thrombosis of intraabdominal or cerebral veins
65
What causes dark urine in acute intermittent prophyria
prophyrins not hemoglobinuria (like in paroxysmal noctrunal hemoglobinuria)
66
lab value change for steroid use for athletics
polycythemia
67
treatment for polycythemia vera
phlebotomy
68
lab values for polycythemia vera
elevated hemoglobin | low erythropoietin level
69
relate urine and sickle cell
hyposthenuria: impairment of kidney's ability to concentrate urine
70
When do you see target cells on peripheral smear
alpha and beta thalassemia
71
What does hemoglobin A2 increase indicate
beta thalassemia
72
lab values for RDW, RBC and Iron/ferritin for both thalassemia
RDW, RBD are low | Iron normal or increased
73
Next step if you see isolated thrombocytopenia without anemia or leukopenia
screen for HIV or Hep C (both cause thrombocytopenia)
74
Pathphysio for thrombotic thrombocytopenic purpura
decrease ADAMTS13 level
75
treatment for thrombocytopenic purpura
plasma exchange
76
pneumonic for thrombocytopenic purpura
``` FAT RN fever anemia thrombocytopenia renal failure neurosymtpoms ```
77
Electrolyte abnormalities in tumor lysis syndrome
Hyperuricemia hyperkalemia hyperphosphateia hypocalcemia
78
Treatment for tumor lysis syndrome
fluids and allopurinol
79
direct antiglobulin test diagnosis what
autoimmune hemolytic anemia
80
impaired gluathione synthesis
G6PD
81
Red blood cell instability
hereditary spherocytosis
82
what vitamin deficiency is common after total or partial gastrectomy
B12
83
B12 is necessary for the synthesis of what
purine
84
Treatment of Vitamin K deficiency
fresh frozen plasma
85
Most common source of symptomatic pulmonary embolism
proximal deep leg veins (femoral vein)
86
abs difference in Waldenstorm marogrlobulinemia and multiple myeloma
WM: IgM MM: IgG or IgA
87
major clinical features for Waldenstorm marogrlobulinemia and multiple myeloma
Wm: hyperviscosity syndrome, hepatosplenomegaly MM: hypercalcemia, osteolytic lesions/fractures
88
Risk factor for Trastuzumab
cardiotoxicity
89
at what age do you stop mamograms
75
90
side effect of bleomycin
pulmonary fibrosis
91
treatment for fibrocystic changes in breast
OCP and NSAID
92
Leukoplakia is a risk factor for what
squamous cell carcinoma
93
most common cause of malignant (nectrotizing) otitis externa
pseudomonas
94
triad of Meniere disease
hearing loss Tinnitus vertigo
95
pathopys for Meniere
increased volume and pressure of enodlymph (endolymphatic hydrops)
96
Loose calcium debris in the semicircular canal
benign paroxysmal positional vertigo
97
inflammation of the membranous labyrinth
labyrinthitis (vestibular neuritits)
98
who has increased incidence of pyogenic granulomas on anterior nasal septum
pregnant women
99
clinical feature of juvenile nasal angiofibroma
epistaxis
100
Treatment of malignant otitis externa
IV ciprofloxacin
101
Treatment for erhlichiosis
doxycycline