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56 Cards in this Set

  • Front
  • Back

Nutrients required for RBC production

Fe, Co, Mn.


B12, B6, C, E, folate, riboflavin, pantothenic acid, thiamine.


Amino Acids

Erythropoiesis regulated mainly by

Erythropoietin


Thryroid hormone


Androgens

Hemoglobin molecule

Synthesized at the polychromatic normoblast stage of red cell development.


Hemoglobin = Heme + Globin.


Hemoglobin = 4 Heme structures with Fe in the center and 2 pairs of Globin chains.

Reticulocyte

Cell just one stage prior to the mature erythrocyte.



Normal Reticulocyte count

0.5 - 1.5%

Stains for reticulocyte count

Methylene Blue


Brilliant Cresyl Blue

Increased Retic Count

Hemolytic Anemia


Response to treatment of Iron / B12 / Folic acid.


Recent Hemorrhage.


Thalassemia.


Pregnancy.


Erythroblastosis fetalis.


HbC disease.


Leukemias.


Hypoxia.

Decreased Retic Count

Decreased adrenocortical and anterior pituitary activity.


Aplastic anemia.


Cirrhosis.


Megaloblastic anemia.


Exposure to radiation.


Anemia of chronic diseases.


MDS

Oversimplification of Retic count

If cause of anemia is inside marrow - decreased Retic count.


If cause of anemia is outside marrow - increased Retic count.

Reticulocyte index

= Reticulocyte count x Patient's HCT/Normal HCT

Reticulocyte Proliferation Index

= Corrected Reticulocyte Count/Shift Correction Factor




PCV 45% = 1


PCV 35% = 1.5


PCV 25% = 2


PCV 15% = 2.5

Hematocrit (HCT) aka...

Packed Cell Volume (PCV)


Erythrocyte volume fraction (EVF)

Formula for HCT

Red cell number x Red cell volume

High HCT/PCV

Dehydration.


Kidney disease with high EPo.


Low O2 level in blood.


Congenital heart disease.


Cor Pumonale.


Pulmonary fibrosis.


High altitude.


Polycythemia vera


Smoking

Low HCT/PCV

Blood loss.


Bone marrow failure.


EPo deficiency.


Hemolysis.


Leukemia.


Malnutrition.


Multiple myeloma.


Autoimmune/Collagen vascular disease like SLE or RA

Note about PCV value:

An elevated PCV may be due to spleen hyperfunction and a low PCV may indicate low thymus function.

Rule of Three....

Hb x 3 = HCT +/- 3


RBC x 3 = Hb




Exception to this rule is in patients with hypochromic red cells. These patients will have hematocrits that are more than 3 times the hemoglobin.

MCV, MCH, MCHC were first introduced by....

Wintrobe

MCV

MCV = (HCT/Red Cell Count) x 100

MCV<72fl with normal RDW

Usually Thalassemia

Anemia with normal MCV - Normocytic Anemia

Acute Hemorrhage.


Dimorphic Anemia.


Hemoglobinopathies.


Anemia due to inadequate blood cell production.


Endocrinopathies (hypopituitarism, hypothyroidism, hypoadrenalism, hypogonadism)


Anemia of chronic diseases.

Anemia with increased MCV - Macrocytic anemia

Megaloblastic Anemia.


Pernicious Anemia.


Sprue.


Macrocytic anemia of pregnancy.


Di Guglielmo disease.


Myelodysplastic syndromes.


Myelophthisic Anemia


Post - splenectomy.


Alcoholism.


Liver disease.


Anemia of hypothyroidism.


Drugs.

Anemia with decreased MCV - Microcytic Anemia

Hypochromic


Iron deficiency


Thalassemia


Lead poisoning


Disorders of Porphyrin synthesis




Normochromic


Anemia of chronic disease (< 1/3rd of the patients)


Heterozygous thalassemia and hemoglobinopathies

Interferences with MCV

Cold agglutinins (increased values)


Warm autoantibodies.


Marked hyperglycemia (increased MCV)


Marked leukocytosis (increased values)


In vitro hemolysis or fragmentation of RBCs (decreased values)


Methanol poisoning (increased values)


Marked reticulocytosis (>50% from any cause) (increases MCV)

MCH

MCH = (Hb/red cell count) x 100

Increased MCH

Macrocytic Anemia


Newborns and Infants

Decreased MCH

Microcytic and Normocytic Anemias

Interferences in MCH

Lipemia


Marked Leucocytosis (>50,000/microL)


Cold agglutinins


In Vivo hemolysis


Monoclonal proteins in blood


High heparin concentration

MCHC

= Hb/HCT x 10

MCHC decreased in

Microcytic hypochromic anemia (Normal value does not rule it out)

MCHC increased in

Hereditary spherocytosis


Infants and Newborns


Autoagglutination


Artifactual

Interferences to MCHC

Decrease


Marked Leucocytosis




Increase


Hemolysis


Cold agglutinins


Severe Lipemia of serums


Rouleaux / RBC agglutinates


High Heparin conc.

RDW

RDW - what is it?

Quantitative measurement or numerical expression of anisopoikilocytosis.

RDW-CV

= (SD of RBC Volume/mean MCV) x 100




Reference values: 11.5-14.5%

RDW-SD

Actual measurement of the width of erythrocyte distribution curve. This measurement is performed at the relative height of 20% above the baseline.




The wider the curve is spread by RBCs of different sizes, the higher the RDW-SD value will be.




Reference values: 35-45 fL.

RDW - Exclusion of two extreme ends of RBC histogram

Excluding extreme left side : Platelets, platelet clumps, and electrical interference.




Excluding extreme right side : Clumped RBCs, overly large RBCs.

Anemia - Normal MCV, Normal RDW

Anemia of chronic disease


Acute blood loss


Acute hemolysis


CLL


CML


Hemoglobinopathy

Anemia - Normal MCV, Increased RDW

Early IDA


Early Vit.B12


Early Folate


Sickle Cell Anemia

Anemia - Low MCV, Normal RDW

Anemia of chronic disease


Thalassemia (heterozygous)

Anemia - Low MCV, Increased RDW

IDA


RBC Fragmentation


HbH


Thalassemia intermedia


G6PD deficiency

Anemia - High MCV, Normal RDW

Aplastic Anemia


Preleukemia


Myelodysplsatic Syndrome

Anemia - High MCV, Increased RDW

Vit B12 deficiency


Folate deficiency


Immune hemolytic anemia


Liver disease


Cold agglutinins


Alcoholism

Gross summary of above combinations

Nutritional disorders - Independent of MCV have increased RDW




Hemolytic disorders - Independent of MCV have increased RDW that is directly proportional to the degree of anemia caused by the disorder.




Hypoproliferative disorders - Independent of MCV have normal RDW

Microcytic, hypochromic RBCs

RBCs are smaller than the nucleus of the small lymphocyte.
Have markedly increased pallor, more than 1/3rd of diameter of RBC.

Causes:
IDA
Thalassemia Minor
Sideroblastic Anemia
Lead Poisoning
Pyridoxine defiency

RBCs are smaller than the nucleus of the small lymphocyte.


Have markedly increased pallor, more than 1/3rd of diameter of RBC.




Causes:


IDA


Thalassemia Minor


Sideroblastic Anemia


Lead Poisoning


Pyridoxine defiency

Macrocytic RBCs

Most of the RBCs are larger than the nucleus of small lymphocyte. (Size >8.5 microns) 

Causes:
Vit B12 or folate deficiency.
Alcoholism
Liver Disease
MDS
Hypothyroidism
Drugs impairing DNA synthesis

Most of the RBCs are larger than the nucleus of small lymphocyte. (Size >8.5 microns)




Causes:


Vit B12 or folate deficiency.


Alcoholism


Liver Disease


MDS


Hypothyroidism


Drugs impairing DNA synthesis

Oval Macrocyte

Causes:
Folate deficiency
Vit B12 deficiency
Pernicious anemia
MDS
Post Chemotherapy

Causes:


Folate deficiency


Vit B12 deficiency


Pernicious anemia


MDS


Post Chemotherapy

Hypochromic macrocyte

Causes:
Alcholism
Hypothyroidism
Liver Disease
Post Splenectomy

Causes:


Alcholism


Hypothyroidism


Liver Disease


Post Splenectomy

Blue Tinged Macrocytes

Causes:
Neonates
Response to Anemic Stress

Causes:


Neonates


Response to Anemic Stress

Target cells aka Bell cells aka Mexican hat cells aka Cododcytes

Characteristic ringed appearance - due to increased surface area to volume ratio - excess membrane pools in the middle of the cells.

Causes:
Thalassemia
Hemoglobinopathies (HbAC/CC/SS/SC)
Liver disease
Post splenectomy
Severe IDA
HbE 
Abetalipo...

Characteristic ringed appearance - due to increased surface area to volume ratio - excess membrane pools in the middle of the cells.




Causes:


Thalassemia


Hemoglobinopathies (HbAC/CC/SS/SC)


Liver disease


Post splenectomy


Severe IDA


HbE


Abetalipoproteinemia

Note about Target cells

In patients with obstructive liver disease, lecithin cholesterol acetyltransferase activity is depressed, which increases the cholesterol-to-phospholipid ratio and produces an absolute increase in the surface area of the red cell membrane. In contrast, membrane excess is only relative in patients with iron-deficiency anemia and thalassemia because of the reduced quantity of intracellular hemoglobin.

Schistocytes aka Schizocytes

Physical damage to RBCs within bloodstream create these cells - include helmet cells, triangles, crescents and microspherocytes.

Physical damage to RBCs within bloodstream create these cells - include helmet cells, triangles, crescents and microspherocytes.



Causes of Schistocytes

Causes:


DIC


Severe hemolytic anemia


Microangiopathic hemolytic anemia


Hemolytic Uremic Syndrome


Prosthetic/Abnormal Cardiac Valve


Coarctation of Aorta


Connective tissue disorders


Burns (spheroschistocytes as a result of heat)


TTP


Uremia, ATN, Glomerulonephritis


Malignant HTN


Systemic amyloidosis


Liver Cirrhosis


Disseminated Carcinomatosis


Chronic Relapsing Schistocytic hemolytic anemia



Tear drop cells aka Dacrocytes

Pear shaped cells usually microcytic, hypochromic.

Causes:
Newborn
Thalassemia major
Leukoerythroblastic reaction
Myeloproliferative syndrome

Pear shaped cells usually microcytic, hypochromic.




Causes:


Newborn


Thalassemia major


Leukoerythroblastic reaction


Myeloproliferative syndrome



Spherocytes

Ball shaped RBCs, decreased surface/volume ratio, hyperdense (>MCHC).

Causes:
Hereditary spherocytosis
ABO incompatibility
Autoimmune hemolytic anemia, 
Microangiopathic hemolytic anemia,
SS disease,
Hypersplenism,
Burns,
Post Transfusion,
Pyru...

Ball shaped RBCs, decreased surface/volume ratio, hyperdense (>MCHC).




Causes:


Hereditary spherocytosis


ABO incompatibility


Autoimmune hemolytic anemia,


Microangiopathic hemolytic anemia,


SS disease,


Hypersplenism,


Burns,


Post Transfusion,


Pyruvate Kinase deficiency,


Water-dilution hemolysis

Elliptocyte

Normally seen in less than 1% of RBC

Causes:
Hereditary Elliptocytosis
IDASS disease and SA Trait
Thalassemia Major
Leukoerythroblastic reaction
Malaria
Megaloblastic Anemia
Any anemia may present with 5-10% elliptocytes

Normally seen in less than 1% of RBC




Causes:


Hereditary Elliptocytosis


IDA
SS disease and SA Trait


Thalassemia Major


Leukoerythroblastic reaction


Malaria


Megaloblastic Anemia


Any anemia may present with 5-10% elliptocytes