role of ADH (2)
1: responds to high osmolarity
V2 receptors: decrease serum osmolarity, increase urine osmolarity
2: respond to low BP
V2 receptors: vasoconstriction
what drains to the popliteal lymph nodes? (2)
2. posterior calf
rx for cluster headaches
oxygen and sumatriptan
rx for migraine abortive?
sumatriptan, NSAID
rx for migraine prophylaxis?
propanolol, topiramate, amitryptaline, Ca2+ channel blockers
rx for tension headaches
NSAID, analgestics, amitryptaline, acetaminophen
acute megakaryocytic leukemia
proliferation of megakaryoBLASTS
AML M7
ITP etiology
antibodies against GpIIbIIIa
SPLENIC macrophage destruction!
ITP blood / bone marrow smear
blood -> thrombocytopenia
marrow -> many mature megakaryocytes
TTP & HUS vs. ITP
all three = thrombocytopenia
TTP / HUS: schistocytes
ITP: splenic destruction
TTP etiology
deficiency of ADAMSTS-13
large platelet vWF -> abnormal platelet aggregation
microthrombi –>
schistocytes & thrombocytopenia
normal anion gap
8-12 mEq/dl
what columns are affected by B12 deficiency?
dry beri beri
B1 thiamine deficiency
peripheral polyneuritis, symmetric muscle wasting
vomit pathway
valine odd chain fatty acids methionine isoleucine threonine
branched amino acids & odd chain fatty acids breakdown into..
methylmalonyl-CoA
—> (methylmalonyl-CoA mutates
succinyl-CoA
acid/base disturbance after salicylate ingestion
first: respiratory alkalosis (hyperventilate)
then SUPERIMPOSED by.. metabolic acidosis (anion-gap)
ultimately: low bicarb (metabolic acidosis) low pH (acidemia) low CO2 (still hyperventilate)
colchicine used for…
GOUT
not RA
etanercept used for..
rheumatoid arthritis
caudal medulla: location of hypoglossal nuc? where does n. leave?
nuc is dorsal
BUT
n. leaves between medial lemniscus & olive! (ventral)
skin ulceration after a vaccine (i.e. tetanus immunization)
due to arthus reaction
edema, necrosis, activation of complement
type III HSR
deposition of antibody, antigen complex
“localized” serum sickness
when does serum sickness occur?
5-10 days post-exposure
antibody against foreign protein –> deposits in membranes
fever, urticaria, arthralgia, proteinuria, lymphadenopathy
wiskot-aldrich vs. chediak-higashi
wiskot-aldrich
chediak-higashi
wiskot-aldrich syndrome presentation
x-linked recessive
defect in actin reorganization
WATER
thrombocytopenic purpura
eczema
recurrent infxn
increased risk of malignancy
and autoimmune disease
B cell immunodeficiency presenting later in life ~20-30 y/o associate w/ autoimmune & RA?
common variable deficiency