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Cast formed at the junction of the ascending loop of Henle and the distal convoluted tubule, may produce structures with a tapered end.
Hyaline casts
Cylindroids have same significance
Hyaline casts
Most commonly seen broad casts
granular and waxy
Reagent strip for glucose turns out negative but the doctor orders a Clinitest
Doctor suspects IEM
Gradual change in the control sample results
Trend
Anti-neutrophilic cytoplasmic antibody
Wegener's granulomatosis
Hematuria, Heavy proteinuria, RBC cast
Henoch-Shonlein Purpura
Genetic disorder showing lamellated and thinning glomerular basement membrane
Alport syndrome
Principle of Micral test
EIA
RBCs in hypotonic urine
Ghost cells
WBCs in hypotonic solution
Glitter cells
Renal calculi may form in
Calyces, renal pelvis, ureters and bladder
Inserted through the nose
Levine tube
Inserted through the mouth
Rehfuss tube
Tubeless test for gastric acidity
Diagnex tubeless test
Principle of Gualac-based test for FOB
pseudoperoxidase activity of hemoglobin
Sperm count equation
Sperm conc. x Specimen volume (mL) = sperm/ejaculate
Odorless urine
Acute tubular necrosis
Glitter cells
Pale blue
PMN granules
violet
Sternheimer-malbin stain
Crystal violet and safranin O; Supravital stain differentiates RTE cells from WBCs and transitional EC
RTE cell
ECCENTRIC NUCLEUS
Transitional epith. Cells
CENTRAL NUCLEUS; May for syncytia or clumps
↑ Specific gravity
Falsely low Nitrite, Proteins and Glucose
Basic tool in evaluating anemia
Stained blood smear
Detectable only by examination of a peripheral blood film
Poikilocytosis
Poikilocytosis
Variation in shape
Abnormal variation in the size of erythrocyte is known as
Anisocytosis
Blood pressure cuff DURING collection is set at
40 mmHg (Harmening)
Not an end cell
Lymphocyte
Kidney or bean shaped nucleus
Metamyelocyte
Sausage shaped nucleus
Band cell
First stage seen with a DMS
Promegakaryocyte
Numerous cytoplasmic granules
Two or more nuclei, No visible thrombocytes
Megakaryocyte
Platelet alpha and dense granules
Organelle zone
Outer surface of platelets
Glycocalyx
Three-part differential
granulocytes, lymphocytes, monocytes
Poikilocyte most commonly seen in hemolytic anemias
Target cell
Hemoglobin at periphery with concentrated central Hb surrounded by area of pallor
Leptocyte
elongated or slit-like area of central pallor disease, hereditary stomatocytosis, or as artifact osmotic changes due to cation imbalance (Na+/K+)
Mouth cell — Stomatocyte
Interior portion of cell is hollow, resembling a horn or helmet; Seen in microangiopathic hemolytic anemias
Helmet cells/horn cells — keratocytes
thin, elongated, pointed ends, crescent shaped; Contain polymers of abnormal hemoglobin S; Seen in hemoglobinopathies SS, SC, SD, and S/B-thalassemia
Sickle cells — drepanocytes
Pear-shaped cell with one blunt projection. Seen in megaloblastic anemias, thalassemia, and extramedullary hematopoiesis (myelofibrosis, myelophthisic, anemia)
Teardrop cell — dacryocytes/dacrocyte
Have evenly spaced round projections; Seen in liver disease, uremia, heparin therapy, pyruvate kinase
Burr cells — echinocytes
unevenly spaced pointed projections; Associated with alcoholic liver disease, post-splenectomy, and abetalipoproteinemia
Acanthocytes - spur cells
Platelet shedding
Mature megakaryocyte
Metamegakaryocyte
Test/s for PNH
Sugar water test
Sucrose hemolysis
Acid-serum test (Ham's test)
higher degree of hemolysis
(+) PNH
Sugar water test
Citrated whole blood
Performed within 2hrs
In the Ham's method for PNH, when the patient has recelved blood transfusions, ______ lysis occurs because of the presence of normal transfused red blood cells
Less
Test using sodium dithionite
Screens for HbS; (+) Turbidity
Solubility test
Metabisulflte is a reducing substance that enhances deoxygenation and sickling (+)
This test cannot differentiate homozygous Hb SS and heterozygous sickle cell trait (Hb AS)
Sodium metabisulfite
Definitive diagnosis of group Hb SS
Hb electrophoresis
Vitamin K dependent group
II, VII, IX, X
Hemophilia A is deficiency of
Factor VIII
Hemophilia B is deficiency of
Factor IX
Hemophilia C is deficiency of
Factor XI
Coagulation factors are assigned a roman numeral
in order of discovery
low platelet count
prolonged PT
prolonged PTT
prolonged TT
What follow up test should be performed?
Presence of FDP/FSP
Sex-linked recessive mode of inheritance
Hemophilia A
Hemophilia B
Autosomal recessive
Hemophilia C
A patient on thrombolytic therapy shows bleeding and the ff lab tests (before heparin)
PTT very long
Fibrinogen very low
DIC
A patient on thrombolytic therapy shows bleeding and the ff lab tests (during heparin infusion)
PTT very long
Fibrinogen low
DIC
has been used in: patients of advanced age; those with leg fractures, cancer or obesity; undergoing hip surgery, varicose vein surgery, or estrogen therapy; those having DIC or CHF, and those with history of venous thrombosis.
Minidose heparin
Monitors patient on oral anticoagulants (Coumadin, Coumarin, Warfarin)
PT (INR)
Monitors patient on heparin
aPTT
Test for extrinsic pathway
Specimen tested within 24 hours
PT
Test for intrinsic pathway
Specimen tested within 4 hours
aPTT
D-dimer is positive in DIC as soon as
4 hours 30
Positive for Philadelphia chromosome
CML
Presence of Ph' chromosome
BETTER prognosis
M1
AML without maturation
M3 — Acute Promyelocytic leukemia
AML with DIC, t(15:17) P' chrom. Auer rods and fag got cells
FAB Classification
>30% Blast cells
WHO Classification
>20% Blast cells
Darkly staining mass of of sex chromosome attached to the end of the nucleus of somatic cells
Barr bodies
macrophages, adipocytes, fibroblasts, endothelial cells
Stromal cells
Predominant cell in the Bone marrow
Metamyelocyte (Juvenile)
Appearance of Primary/ nonspecific granules
Promyelocyte
Appearance of secondary/specific granules
Myelocyte
Leukocytosis
WBC > 11x10^9/L
Number of lymphocytes is greater than the number of PMN present in the sample
200 differential count
Correction of WBC count
Adult ≥ 5 NRBCs/100
Neonate ≥ 10 NRBCs/100 WBC
Poor man's platelet aggregation study
Examination of blood film of fresh capillary blood
Best way to make smear
Smooth and rapid
Thin blood smear
Smaller drop of blood
Slower spread
Lower angle
Thick blood smear
Larger blood drop
Fast spread
Higher angle
The needle used in the evacuated tube system (ETS) is _______ ended.
Double
Third layer on spun hematocrit
Buffy coat layer
Overcentrifugation
No effect on Hb (HICN method)
Decreased ESR and Hct
Coagulation specimen
Centrifuged within 1 hour
PPP (Coagulation studies)
Centri 1,500g for 15 mins
PRP (Aggregometry studies)
Centri 50g for 30 mins
Higher in the afternoon
Eosinophils
If the stain cannot be performed immediately, the unfixed smears may be stored in the dark at room temperature for up to two weeks without significant loss in activity
Chloroacetate esterase
Differentiate acute myelogenous and myelomonocytic leukemias from acute lymphocytic leukemia
Sudan Black B
Macrocytosis of 25%-50% is graded as
2+ to 3+
Hemolyzed sample for coagulation testing
REJECT
Manual detection of fibrin clot formation
Tilt tube method
Wire loop
Electromechanical
Fibrometer