Heme/Onc - bleeding/hypercoag - quiz Flashcards
5 yr old boy - thrombocytopenia - abnormal GFR - recent diarrhea - schistocytes
HUS
HUS treatment
supportive; no antibiotics
48 yr old woman - thrombocytopenia - fever - delirium - schistocytes
TTP
TTP treatment
plasmaphoresis
33 yr old woman - stroke - hx 4 miscarriages
lupus anticoagulant
45 yr old woman - first DVT/no history - what do you want to check for?
malignancy
most common systemic vasculitis in children
Henoch-Schonlein purpura
4 yr old boy - palpable purpura over lower extremities - arthritis in knees and ankles
Henoch-Schonlein purpura
treatment for Henoch Schonlein purpura
prednisone
most common inherited bleeding disorder
von willebrand disease
initial treatment for ITP
corticosteroids
treatment for recurrent/relapsing ITP
splenectomy
your immediate handling of HIT
- discontinue heparin
- U/S LE for thrombosis
- give direct thrombin inhibitor
one key difference in labs for vit K deficiency and coagulopathy of liver disease
factor V: not impacted by vitamin K; decreased in CoLD
sudden thrombosis (3)
- polycythemia vera
- essential thrombocytosis
- HIT
essential thrombocytosis treatment
aspirin
hydroxyurea
polycythemia vera lab value
extremely elevated Hct
essential thromocytosis lab value
extremely elevated platelets
polycythemia vera treatment
phlebotomy; NO iron supplementation
polycythemia vera: erythropoietin high or low?
low (high RBCs not caused by high erythropoietin - in fact, high RBCs cause low erythropoietin)
JAK2 associated with (3)
- polycythemia vera
- essential thrombocytosis
- myelofibrosis
striking splenomegaly
myelofibrosis
compare bone marrow of aplastic anemia, pure red cell aplasia, myelodysplasia
aplastic anemia: hypocellular
pure red cell aplasia: normocellular
myelodysplasia: hypercellular
compare organ size of aplastic anemia, pure red cell aplasia, myelodysplasia
aplastic anemia: no organomegaly
pure red cell aplasia: no organomegaly
myelodysplasia: splenomegaly
IgM binds RBC antigen in lower temps
cold agglutinin disease
IgG binds RBC antigen at body temp
autoimmune hemolytic anemia
onset around 6 mos old
beta thalassemia; sickle cell disease
anemia definition
hct < 41 (male) <36 (female)
basophilic stippling
beta thalassemia
“bite” cells
G6PD disease
3 platelet inhibitors
aspirin, clopidogrel, ticlopidine
3 anticoagulants
warfarin, dabigatran, heparin/LMWH