Plasma Cell
Oxygen and Hgb
Blood Smear
CMPD
RBC Poik/Inclusions
100

Area adjacent to the nucleus of a plasma cell

golgi; perinuclear halo

100

Hemoglobin form not measured by cyanmethemoglobin

Sulfhemoglobin

100

Neutrophils and RBCs appear blue

Overstained

pH too alkaline

100

A patient with normal Hgb and WBC counts, persistently elevated platelet counts (>100,000,000/ul), increased marrow megakaryocytes and a history of frequent bleeding most likely has:

ET

100

RBC inclusion only visible with supra vital stain

Heinz Body

200

Major peripheral smear finding associated with plasma cell disorders

Rouleaux

200

Levels of CO2 and 2,3 DPG associated with right shift.

Associated pH with a right shift.

Increased

Acidic

200

3 causes of platelet clumps

Short draw

Clotted sample

EDTA-induced

ET

200

2 diseases associated with defective ROS production by neutrophils

CML

IMF

CGD

200

A term used to describe a mature RBC that contains iron granules or deposits

Siderocyte

300

4 common features of all P.C. disorders

Rouleaux

Increased ESR

Hyperviscosity

Bence jones

M-spike

P.C. (or plasmacytoid) in B.M.

300

3 interferences of the cyanmethemoglobin method

High WBC

Lipemia

Lyse resistant RBCs (sickle cells)

300

4 artifact causes of burr cells

Artifact:

Excess EDTA

H2O contamination

Slow drying

Increased humidity

Blowing

Old Sample

300

Polycythemia associated with:

Hgb 25 g/dL

Hct 60%

O2 Saturation: normal

Smear: Microspherocytes, schistocytes

Relative Polycythemia

300

3 peripheral findings associated with Hgb SS 

Sickle cells

Target cells

Schistocytes

Polychromasia

nRBCs

400

P.C. associated with plasmacytoid lymphs

Waldenstroms

400

A cellulose acetate was performed on a stillborn infant revealed a single band that migrated further toward the anode than the Hgb A control.  What is the composition of this band?

4 gene deletion-hydrous fetalis

Hemoglobin barts (gamma)

400

Megaloblastic triad

Hypersegs

MCV > 100 fL

Macroovalocytes

(Bonus-Pancytopenia)

400

Which of the following is not a cause of absolute secondary erythrocytosis?

Defective cardiac or pulmonary function

High altitude adjustment

Dehydration due to diuretic use

Hemoglobin with increased oxygen affinity

Dehydration due to diuretic use

400

Which of the following blood findings LEAST likely correlates with the presence of ringed sideroblasts in the bone marrow?

Pappenheimer bodies

Basophilic stippling

Decreased TIBC

Siderocytes


Decreased TIBC

500

P.C. disorder associated with Russell Bodies

Multiple Myeloma

500

A cellulose acetate revealed a band in the Hgb S position.  This band was 95%.  The peripheral smear showed 70% target cells and the solubility test was negative.  

Based on the information, what is the hemoglobin?

Hemoglobin D

500

An adult WBC count was 4.0x103/ul.  The differential was: PMNs 25%, bands 5%, lymphs 65% and monocytes 5%.

There is:

absolute lymphocytosis

relative lymphocytosis

both relative and absolute

relative

500

4 differences between CML and leukemia reaction

Toxic changes (L)

Ph' chromosome (C)

Basophilia/Eosinophila (C)

LAP increased (L) LAP decreased (C)

500

4 Poikilocytosis/slide abnormalities associated with a short draw

Crenated WBC

Crenated RBC

Platelet clumps

Giant platelets

Platelet sat elitism