UA final review Q's 2 Flashcards
10 mo. old is pale and listless upon physical examination, chiro ordered a CBC, platelet count, total serum iron and ferritin study. results are: HCT=24 & MCV=68.6
microscopic reveals significant anisocytosis, microcytosis, hypochromia, and piokilocytosis. a normal distribution of platelets was present. stool and urine studies are negative for blood or parasites. what category of anemia is suggested by the morphology of the RBC’s and blood results.
iron deficiency
what other signs on inspection would aid you in ur dx?
-swelling of the tongue
-dry lips
-craving for ice chips
(all the above)
the second leading cause of anemia worldwide is
chronic disease
the infectious microorganism directly associated with hemolytic uremic syndrome is
E-coli 157-07
a risk factor for vitamin B-12 anemia is:
vegetarian diet
a pt. presents with abdominal distress, neurological disturbances and trouble seeing yellow and blue. you would order:
vit B-12 study
which of the following is not associated with hemolytic anemia
increased haptoglobin
john presents in ur office with dyspnea, jt. pain and fatigue. he is a 25 yoa black male who has experienced these symptoms on and off for several years. the crisis seem to come and go. what factors contribute to the erythrocyte disorder you suspect in this pt.?
sickling is spontaneous
which of the following dx tests would provide aid in conformation of your suspicions? (john)
-CBC
-UA
-microscopic blood analysis
(all the above)
what is the condition u would suspect?
sickle cell
john’s prob. can be corrected by?
cannot be corrected bc its genetic in nature
with iron deficiency anemia, u would suspect?
low MCV low hematite and low MCHC
which of the following anemias are megaloblastic?
- B12 deficiency
- & folate deficiency
cobalamin transport out of the gut is mediated by:
intrinsic factor
aplastic anemia can be caused by:
-infection
-EBV
-radiation
(all the above)
pts. with aplastic anemia need to be identified quickly as it will progress quickly and result in death. T/F?
true
in a pt. with hereditary spherocytosis you would expect to ind this on palpation of the abdomen:
enlarged spleen
in sickle cell anemia the pt. possesses an abnormal form of hemoglobin called:
hemoglobin S
u receive a lab report on a pt. and u notice the number of WBC is 450,000. u would suspect?
leukemia