Intro Flashcards

1
Q

Hemoglobin (Hgb) in grams per deciliter (g/dL) are ………….
Hematocrit (Hct) or packed cell volume (volume of RBCs as a percent of total blood volume), pcv
…………..

RBC count :normal………

Reticulocyte: Retic Count……….

A

Male: 13-18 g/dL and Female: 11.5-16.5 g/Dl

41% to 52%. Normal level for women is 36% to 48%.

4.5-6.5 million cells/mcL.

0.5 to 2.5% indicates

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2
Q

Hypochromia

Macrocytosis

Rouleaux

Schistocytes ( Fragmented RBCs):

Spherocytes

Target cells

Burr cells(“echinocytes

Howell-Jolly body :

Basophilic stippling

Bite cells ,Heinz body, Blue dots in RBC:

Acanthocytes Cells

Teardrop cells (“dacrocytes”

Elliptocyte cells

A

> 1\3 to 1/2 of the cell diameter

Increased RBC size(MCV > 110 fL) Megaloblastic anemia; liver disease; reticulocytosis;
myelodysplastic syndromes; alcoholism

RBCs in long lines or stacks Hypergammaglobulinemia; monoclonal gammopathies

Mechanical trauma: malfunctioning prosthetic heart valve;
thrombotic microangiopathy (TTP/HUS); severe burns; joggers; severe shock or acidosis; severe intravascular hemolytic anemia.

Small round cells with no central pallor Hereditary spherocytosis; immune hemolytic anemia.

Central thick area surrounded by pale ring as in Liver disease; hemoglobinopathies (thalassemia, sickle cell anemia)

Cells with relatively even spicules around periphery; central pallor preserved.As in Renal failure; often seen as artifact on blood smears (“crenated cells”)

Small round fragment of nuclear material in RBC occur in Splenectomy; sickle cell anemia.

RBCs with fine to coarse bluish speckles as in Lead poisoning; thalassemias; any severe stress on the bone marrow.

seen in Unstable hemoglobin; Unstable hemoglobins; hemolytic anemia due to enzyme deficiencies (G6PD deficiency).

irregular shape a few long projections no central pallor occur in Severe liver disease;; abetalipoproteinemia; severe starvation.

RBCs shaped like teardrops with one pointed end, as in Extramedullary hematopoiesis; myelophthisic anemias (myelofibrosis, space-occupying lesions in bone marrow.

oval or elongated, from slightly egg-shaped to rod or pencil forms.Mutations in genes coding for protein 4.1, alpha spectrin, beta spectrin, band 3, and Glycophorin C have all been implicated in hereditary elliptocytosis

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3
Q

Causes of leucopenia

A

bone marrow suppression like leukemia, lymphoma, aplastic anemia, post chemotherapy and connective tissues disorders like systemic lupus erythematosis and others .

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4
Q

Normal count of neutrophil range

A

40% to 60% of total WBCs

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5
Q

Common causes of neutrophilia

A

bacterial, fungal infection, truma, surgery, burn, myocardial infarction, pulmonary embolism, sicke cells crises, pregnancy exercise and others

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6
Q

Common causes of neutropenia

A

infection like viral ,bacterial as typhoid fever ,protozoal as malaria, autoimmune disease ,bone marrow suppression as aplastic anemia, leukemia ,alcohol, drugs like(carbimazole ,captoprile, cimetidine ….others)

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7
Q

The normal eosinophil counts

A

<0.5 x 109/L) ~1 to 4%of total WBC.

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8
Q

Eosinophilia

A

eosinophilia connective tissue disorders as polyarteritis nodosa ,malignancy as lymphoma and leukemia. Hypereosinophilia: (HE, persistent peripheral blood eosinophilia > 1.5 × 109/L) <8%of total WBC.

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9
Q

Basophilia

A

myeloproliferative disease ,ulcerative colitis and crohns disease

involved in immediate hypersensitivity reactions related to immunoglobulin class E (IgE) .

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10
Q

.normal count Lymphocytes

A

20–40% of WBC)

1,5—3.5 x109/L

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11
Q

Causes of lymphocytosis

A

viral infection ,bacterial (bordetella pertussis),chronic lymphocytic leukemia,acute lymphoblastic leukemia, lymphoma.

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12
Q

Causes of lymphopenia:

A

Covid19, AIDS, viral hepatitis, tuberculosis, and typhoid fever.Connective tissue disorders like systemic lupus erythematosis, renal failure, drugs like chemotherapy, corticosteroid.

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13
Q

Causes of monocytosis

A

Bacterial infections: tuberculosis, subacute bacterial endocarditis, and brucellosis. Other infections: Syphilis, viral infections (eg, infectious mononucleosis), and many protozoal and rickettsial infections , kala azar, malaria, .Chronic inflammatory diseases as ulcerative colitis ,crohns disease and malignancy.

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14
Q

Common causes of thrombocytosis are

A

Essential thromcytosis, Hemorrhage,Iron-deficiency anemia,Rheumatoid arthritis and vasculitis .

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15
Q

Common causes of thrombocytopenia

A

I.T.P(idiopathic thrombocytopenia purpura,).systemiclupus erythematous(SLE).Disaminated intravascular coagulopathy( DIC), postchemotherapy, Malignancy and Aplastic anemia

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16
Q

For the average adult, the bone marrow produces

A

5 x 1011 cells per day

17
Q

Hematopoiesis begins in

A

yolk sac during the first month of embryogenesis but gradually shifts to the liver and, to a lesser extent, the spleen. The liver is the primary site of hematopoiesis during the second trimester; however, the bone marrow becomes the primary site of hematopoiesis after the seventh month. After birth, the bone marrow is normally the sole site of hematopoiesis (intramedullary hematopoiesis).

18
Q

Expression of ……… a marker of immature cells, is used as a marker for hematopoietic stem cells.

A

CD34

19
Q

Granulocytopoiesis

A

Myeloblast then Promyelocyte then Myelocyte followed by Metamyelocyte then Band neutrophil and Segmented neutrophil.

20
Q

Erythropoiesis

A

Proerythroblast then Basophilic erythroblast then Polychromatophilic erythroblast then Orthochromatophilic erythoblast followed by Reticulocyte finally Erythrocyte