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51 Cards in this Set
- Front
- Back
t/f
splenomegaly is never benign |
true
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Massive splenomegaly is caused by all of the following except?
-myeloproliferative disease -cirrhosis -malaria -myelofibrosis -gaucher's -kalazar |
cirrhosis; massive is caused by the 3 M's along with gaucher's and kalazar
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What does the splenomegaly mneumonic CHINA stand for?
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c-congestion (portal)
h-hematological i-infection n-neoplasia a-autoimmune |
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t/f
the normal spleen is not palpable |
true
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what are the 4 RBC components?
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cell membrane
hgb iron enzymes |
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a common cell membrane disorder could be?
-Iron deficiency anemia -sickle cell disease -spherocytosis -G6PD deficiency |
hereditary spherocytosis
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what is the best 1st test to diagnose hereditary spherocytosis?
-peripheral blood smear -ELISA -osmotic fragility test |
osmotic fragility test
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variations in cell size is referred to as?
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anisocytosis
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a pt with Fe def. anemia will have a _ RDW on CBC.
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increased
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a pt with Thalassmia will have _ RDW on CBC.
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normal
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_ is a quantitative measure of the degree of anisocytosis.
-MCH -MCHC -RDW -retic. count |
RDW
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the RDW is useful in the diagnosis of _ anemia.
-microcytic -normocytic -macrocytic |
microcytic
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Enumerating reticulocytes therefore gives a measure of marrow _ _ production.
-hemoglobin -white blood cell -red blood cell |
red blood cell
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t/f
the lower the retic count the more hemolysis there is. |
false; the higher the retic count the more hemolysis there is.
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increased production of RBC's in the marrow can be caused by all of the following except?
-high elevation -bleeding -some anemias -spherocytosis |
not spherocytosis
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the retic count usually _ after successful treatment for pernicious anemia, iron deficiency anemia or folic acid deficiency anemia.
-lowers -raises -normalizes |
raises
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where is iron stored?
-ferritin -transferrin -hemoglobin -liver |
ferritin
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what is the first best test to order in a pt you think is anemic?
-cmp -cbc -iron -ferritin |
cbc-to check hgb/hct
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what is the most accurate test to diagnose iron def. anemia?
-cbc -h & h -bone marrow -ferritin |
bone marrow
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An anemic pt with a normal ferritin level = ?
-iron deficiency -folate deficiency -thalassemia |
thalassemia
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If an anemic pt has a normal MCV, but an elevated retic count what do you have?
-iron deficiency -renal disease -hemolysis |
hemolysis-get B12 and folate
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Hearsay exceptions declarant must be unavailable.
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1. Former testimony
2. Statement against interest 3. Dying declaration 4. Forfeiture (D caused the witness to be unavailable) |
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Any pt over 40 y.o. with iron deficiency anemia is _ cancer until proven otherwise.
-colon -breast -stomach -pancreatic |
colon
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in what type of deficit will a pt c/o neuropathy?
-folate -iron -B12 -ferritin |
B 12 deficiency
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A pt has B 12 and folate deficiency, what social habit must you ask about?
-smoking -diet -alcohol |
alcoholism
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What is the age of reticulocytes?
-<24 hours -<48 hours -<3 days -<7 days |
< 48 hours
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what do CRP, ESR, platelets, and ferritin all have in common?
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acute phase reactants
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A 60 y.o. male pt has a hgb of 10, MCV 69, ferritin 6 (low). He also admits to occasional blood in the stool, with alternating diarrhea and constipation. What is your diagnosis, and what is your plan?
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Iron deficiency anemia, he needs a rectal exam with a follow up colonoscopy
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A 22 y.o. female from Italy, is admitted to you for syncope, on routine lab work she has a hgb 10.2, MCV 66, plts 270, the pt's iron and ferritin levels are normal, HbA2 is 5.5% (high). What does she have?
-B12/folate deficiency -thalassemia -iron deficiency -spherocytosis |
thalassemia-beta
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a 61 y.o. female is admitted for SOB on excertion x2 months with ambulation unsteadiness. Her labs show WBC 3.1, Hgb 6.1, MCV 136, plts 110. She denies smoking, alcohol, and eats a regular diet. Her folate is nml 39, B12 is low. What do you have?
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macrocytic anemia with pancytopenia.
Pernicious anemia |
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t/f
ferritin is the transport protein for iron, not for storage |
false; ferritin IS the tissue storage protein for iron, NOT a transport protein
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A 32 y.o. man comes in c/o bruising and generally not feeling well for 2 weeks. His WBC 11.5, hgb 8.3, MCV 95, Plt 20, Blasts 112.7. What do you suspect?
-viral infection -lymphoma -leukemia -multiple myeloma |
leukemia
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if you suspect leukemia, what is the most important test?
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bone marrow biopsy
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a pt presents with abdominal discomfort, you find moderate splenomegaly, elevated retic count, low haptoglobin, elevated indirect bilirubin, and a + osmotic fragility test. What does your pt have?
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hereditary spherocytosis
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All of the following are true about sickle cell anemia except?
-will see nucleated RBC's -Howell-Jolly bodies -schilling test is diagnostic -usually autosplenectomy by age 10 -hydroxyurea can reduce # of flareups |
schilling test is not even available
hemoglobin electrophoresis confirms diagnosis |
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A 63 y.o. woman admitted for tx of severe/active RA. WBC 2.8, hgb 8.9, MCV 69, plts 91. spleen is enlarged, iron low, ferritin is low normal. What type of anemia does she have? What else do you know?
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microcytic anemia with moderate pancytopenia
Felty's syndrome=pancytopenia, splenomegaly and hypersplenism |
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heavy plasma cell infiltrate on a bone marrow biopsy indicates?
-leukemia -lymphoma -multiple myeloma |
multiple myeloma
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heavy plasma cell infiltrate on a bone marrow biopsy indicates?
-leukemia -lymphoma -multiple myeloma |
multiple myeloma
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heavy plasma cell infiltrate on a bone marrow biopsy indicates?
-leukemia -lymphoma -multiple myeloma |
multiple myeloma
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for hemoglobinapathies the most accurate diagnostic test is ?
-blood smear -hgb electrophoresis -serial cbc's |
hgb electrophoresis
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for hemoglobinapathies the most accurate diagnostic test is ?
-blood smear -hgb electrophoresis -serial cbc's |
hgb electrophoresis
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for hemoglobinapathies the most accurate diagnostic test is ?
-blood smear -hgb electrophoresis -serial cbc's |
hgb electrophoresis
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Iron deficiency anemia is most often secondary to ____.
-gi bleed -multiple myeloma -malabsorption |
gi bleed
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Iron deficiency anemia is most often secondary to ____.
-gi bleed -multiple myeloma -malabsorption |
gi bleed
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pallor, glossitis, angular cheliosis, koilonychia, Plummer Vinson syndrome are all indicative of?
-Folate deficiency -B12 deficiency -iron deficiency |
iron deficiency
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pallor, glossitis, angular cheliosis, koilonychia, Plummer Vinson syndrome are all indicative of?
-Folate deficiency -B12 deficiency -iron deficiency |
iron deficiency
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Iron deficiency anemia is most often secondary to ____.
-gi bleed -multiple myeloma -malabsorption |
gi bleed
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pallor, glossitis, angular cheliosis, koilonychia, Plummer Vinson syndrome are all indicative of?
-Folate deficiency -B12 deficiency -iron deficiency |
iron deficiency
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Plummer-Vinson syndrome =?
-colon skip lesions -esophageal string bean -esophageal webbin |
eso. web
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Plummer-Vinson syndrome =?
-colon skip lesions -esophageal string bean -esophageal webbin |
eso. web
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Plummer-Vinson syndrome =?
-colon skip lesions -esophageal string bean -esophageal webbin |
eso. web
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