Anemias Flashcards
Neutrophilia Causes
Bacterial infection (most common)
Some viral and fungal infections
Chronic Inflammation
Smoking, exercise, stress
Leukemoid Reaction vs. CML
Leukemoid Reaction: WBC <50, left shift, normal RBC, normal platelets, LAP increased, philadelphia chromosome absent
CML: WBC >50, left shift, low RBC, varying platelets, LAP decreased, philadelphia chromosome present
Neutropenia
Range, conditions
Absolute neutrophil count <1.5 x 10^3/uL
Decreased bone marrow production: aplastic anemia
Increased cell loss: anemia, chemotherapy
Pelger Huet Causes
Leukemia or myelodysplastic syndromes
Hypersegmented Neutrophils
causes
Megaloblastic anemia, B12, folate deficiency
Dohle Bodies
Severe infections, burns, cancer, toxic drugs
Toxic Granulation
Bacterial infections
Alder-Reilly
Normal function, large granules
Chediak-Higashi
Symptom, diff, inclusions
Early death, recurrent infections, neutropenia, thrombocytopenia, blue-green bodies
May-Hegglin
Inclusions? Smear?
Inclusions that look like Dohle bodies
Giant platelets, low platelet count, bleeding
Chronic Granulomatous Disease
Respiratory burst oxidase system, cannot generate oxygen to kill microorganisms
Form granulomas around pathogens in tissue
Reticulocytes
What are they, stain qualities,
Immature red blood cells with increased RNA
On wright stain, polychromatophilic cells
On new methylene blue supravital stain, blue granules
Reticulocyte Smear Procedure
1:1 ratio of blood to new methylene blue
Incubate for 15 minutes at room temperature in the stain
Miller Disc Formula
% retic = (# retics counted x 100) / (# RBCs counted x 9)
Count at least 112 RBCs, should have 5-7 RBCs in little square
RPI and Corrections
If pt HCT <45%
(% retic count / maturation time) x (patient HCT/45)
RPI Interpretation
<2.0: decreased production, Fe deficiency, aplastic anemia
>2.0: increased destruction, hemolytic anemia
Absolute Retic Count Formula
(% retic x RBC should be given) / 100
Sickle Cell Trait vs. Disease
Which is worse?
Sickle cell trait has one copy of mutation, not as many symptoms unless under low oxygen tension
High Pressure Liquid Chromatography (HPLC)
What does it do, patient population
Separates and quantifies hemoglobin
Newborn screening
Done before electrophoresis
Sickle Quick
Screens for, procedure, interpret, bad for
Screens SS disease and AS trait
RBCs lysed and hgb released, HgS is insoluble, will form turbid suspension in phosphate buffer
False positive in HbC Harlem or low hemoglobin
Bad test for babies, false negative from HgF
Electrophoresis
What does it do, order for alkaline and acid, traveling trends
Identifies hemoglobin proteins based on electrical charges
Alkaline: CSFA
CEO, SDG travel together
H and Barts faster than A (won’t show up)
Acid Citrate: FASC
ADGEO travel together