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1 Haematology actualy hematology is the science that deals with blood elements Blood elements RBCs , WBCs and coagulation science of investigation not science of clinical diagnosis hematologist investigations RBC physiology RBCs IntraUterina 3 rd week yolk sac liver and spleen fourth month BoneMarrow Bone marrow limited to end of long bones and flat bones hemolytic anemia bone marrow proliferating replace RBCs proliferate shaft shaft spleen liver & and bone marrow expansion hepatosplenomegaly RBCs BM stem cells undifferentiated rbcs , wbcs or platlets cells RBCs pleuripotent cells stage RBCs

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  • 1

    Haematology

    actualy

    hematology is the science that deals with blood elements

    Blood elements

    RBCs , WBCs and coagulation

    science of investigation not science of clinical diagnosis

    hematologist investigations

    RBCphysiology RBCsIntraUterina 3rd weekyolk sac

    liver and spleen

    fourth month BoneMarrow

    Bone marrow

    limited to end of long bones and flat bones hemolytic anemia

    bone marrow proliferating replace RBCs

    proliferate shaft shaft spleen liver &

    and bone marrow expansion hepatosplenomegaly

    RBCs BM stem cells undifferentiated

    rbcs , wbcs or platlets cells RBCs

    pleuripotent cells stage RBCs

  • 2

    RBCS nucleasstem cellnucleus nucleus

    RBCSreticulocytes reticulocytes

    bone marrow Mature RBCs Mature RBCs

    RBCs 2%maximum 2 %

    haemolysis RBCs bone marrow

    reticulcytes immature reticulcytes

    haemolysis and haemorhhage reticulcytesanemia medical treatment

    iron deficnecy anemia Bone marrow RBCs iron iron

    reticulcytessuccess of treatment reticulcytosis

    reticulcytes bone marrow failure pan

    cytopenia hypersplenism or bone marrow failure reticulcytes

    bone marrow failure hypersplenism spleen reticulocyte

    bone marrow activity

    Reticulocytosis reticulocytes

    reticulocytesRBCs reticulocyte

    Macrocytosis large cells in blood

    COUNT RBCs

    Male : 4-6 Mil

    Female : 3.5 to 4.5 Mill

    femaleMale female =D Androgen stimulate

    production of RBCs menstrual cycle 35 ml

    Female androgen male =D

    Bone marrow failure androgen Androgen

    stimulate production of RBCs

    CountRBCs polycythemia

    shapebiconcave sicke cell ad spherocytes

    hematocritepacked cell volume

    hematocrite 011011centrifuge centrifuge

    RBCs plasma 55 ,RBCs 5555Hemtaocrite 011

    55packed RBCs

  • 3

    hematocriteanemia hypervolemia anemia hypervolemia

    diluted

    dehydration or polycythemia hematocrite

    hypervolemia

    01212

    RBC mean corpuscular volyme

    hematocrite count RBC mean corps volume

    45 ml5 million 90 U3range 86 69RBC

    69Microcyte 69macrcyte range

    normocyte mcq RBcs

    size RBC diameter of RBCMicroscope ,

    97.6micron 97.microcyte 6macro 02megalo

    megalo macro macor megalo

    Macrocyticmegaloblastic

    macrocytic non megaloplastic

    haemoglobin

    Male : 14-16

    Female 13.5-14

    anemia polycythemia

    haemoglobin RBC 01010

    15gm hemoglobin RBCs

    hemoglobin RBC ular haemoglobinmean corpusc055

    30 Pgrange 2602heamoglobin RBC

    hemoglobin RBC hyperchromic

    hemoglobin RBC hypochromic mean

    corpuscular haemoglobin hypo , hyper or normochromic

    mean corpuscular hemoglobin concentration hematocrite

    the value of blood film in diagnosing anemia

    size , shape , count , mean corpuscular volume

    items 01the value of blood

    smear

    ESRgnancy maliinflammation and infection ,

  • 4

    ESR Capillary tube

    blood RBCs RBCs

    5ESR 5RBCs

    2 hours 6

    RBCs RBCs should be attached

    to eacth other RBCs negative charge Repulsion

    albumin negative charge nephrotic syndrome albumin negative

    charges ESR albumin negative charges RBCs

    ESR

    globulin and fibrinogen negative charges from RBCs globulin infection and

    inflammation

    ESR

    fibrinogen pregnancy negative charges ESR

    ESR and malignancy , Infection and inflammation , pregnancy and nephrotic syndrome

    malignancy antibodies

    ESR RBCs Charges

    MCQ ESR 0110Malignancy , TB collagen disease

    abnormal shape of rbcs MCQ

    Value of blood film in diagnosin anemia

    general rules

    general rules

    General rules anemia

    Anemia by definitionin or hematocrite in same age sexanemia is the decrease in RBCs or hemoglob

    and race

    hemoglobin 14 is abnormal 09adult

    Sex female 02male

    Race negros low hemoglobin Caucasian

    050diluted

    02anemic ?anemic actually am not

    dehydrated 0.polycythemia

    General Rules

  • 5

    sex , age and race

    RBCs

    01

    anemic is it possible to do this ?

    chromium or technetium IV RBCs RBC

    gamma camera technetium labeled RBCs

    RBCs

    anemia hypervolemia hypervolemia

    RBCs RBCs

    not practical

    classification of anemia acc to etiology acc to morphology

    Acc to etiology

    etiological

    enough

    deficiency anemia hemoglobin

    RBCs Bone marrow anemia of bone marrow

    failure hemorrhage and hemolytic anemia

    according to etiology Deficiency anemia , Anemia of bone amrrow failure , hemorrhage and

    hemolytic anemia

    morphologynormocytic normochromic anemia

    microcytic hypochromic microcytic 69hypo chromic

    28

    Microcytic hypochromic anemia

    Microcytic hypochromic anemiaheme and

    globulinheme iron + heme globulins heme iron

    deficiency anemia

    globulin thallassemia

    Normocytic normochronic anemiaRBCs acute

    hemorrhage , acute hemolysis ,bone marrow failure

  • 6

    Macrocytic anemiamegaloblastic02non megaloblastic 602megaloblastic

    Vb12 and folic acid non megaloblastic liver cell failure reticulocytosis

    RBCs reticulocytosis macrocytic anemia

    reticulocytes

    Macrocytic non megaloplastic liver cell failure , alcoholism and reticulocytosis

    classification of anemia

    general rules physiology etiology

    iron deficiency anemia physiology of iron etiology

    iron absorbtion HCL etiology

    of iron deficiency anemia HCL

    Clinical picture FOG P

    FFatigue decrease of o2 delivery to tissue

    F fundus hypoxia vasodilatation retinal edema

    blurring of vision

    OOedema edema vaso dilatation tissue hypoxia

    anemic HR sever anemia and long standing acute anemia Heart

    failure

    consent

    hemoglobin 075Heart failure

    acute Heart failure

    edema vasodilatation peripheral vasodilatation GIT

    Git congestion malabsorbtion anorexia hypoprotenemia

    GIT Congestion

    G eneral systemsGCNS , CVS , Respiratory , Renal CNS Vasodiltation CNS cerebral edema headache

    hypoxia of nerve , peripheral neuritis

    headache , anorexia and bluring of vision tumor

    pseudo tumor cerebri

    it has similar features like a brain tumor

    CVS hyperdynamic circulation palpitation , tachycardia ,severe long standing anemia Heart

    failure

    Renal polyurea VD Renal blood flow Nocturia

    specific features

    FOG P anemia jaundice haemolytic

  • 7

    specific

    specific feature C/P of the causeFOG P spooning

    of nails iron deficiency anemia epigastria pain and constipation

    C/P of the cause etiology

    FOG P specific feature C/P of the cause

    RBCs hematocrite ESR 2

    MCV & MCH

    microcytic hypochromic or macrocytic

    specific investigationhemoglobin

    hematocrite MCV .9microcytic hypochromic iron deficncy

    anemia thalassemia iron level iron deficncy thalassemia

    specific investigationhemoglobin MCV 61

    BM failure hemolytic or hemorrhage reticulocyte Bone marrow failure

    Investigation of the cause

    MCV .0microcytic anemia iron

    iron deficncy anemia stool analysis for parasite

    Treatment 0 Tratemnt of cause

    2 Blood transfusion if HB

  • 8

    iron blood transferrin transferring

    Iron

    010iron .iron Transferrin saturated ,

    01 % total binding capacity

    iron deficncey transferrin saturation

    total iron binding capacitytransferrin iron

    Muscles myoglobin

    tissue enzymes enzymes iron catalase

    liver ferrtitin

    physiology

    Etiology Starvation , malnutrition *

    diminced HCl 9milk

    9female iron 99

    iron deficiency

    stomack HCL atrophic gastritis , gatsrectomy gastrc carcinoma

    duodenum malabsorbtion

    congenital rare

    chronic blood loss Iron deficiency anemia

    parasite and menstrual irregularity

    parasite parasite anclystoma

    51iron deficiency anemia cancer colon

    colonoscopy peptic ulcer virus hemoptysis

    hematuria

    clinical picture

    0 FOG P

    2 specific enzymes affect metabolism

    0 tissues metabolism proliferate tissue proliferating tissue proliferate

    skin an GIT

    SKIN proliferation and replacement iron deficiency loss of hair and

    spooning of nails

  • 9

    GIT papillae proliferation and

    replacementproliferation red glazed tongue

    clinical picture of the cause

    diminished absorption gatsrectomy

    parasite manifestations epigastria pain constipation and pellagra

    Plummer Vinson syndrome ?

    cancer esophagus female splenomegaly dysphagia

    Investigations

    RBCs hematocrite ESR

    Type of anemia : microcytic hypochromic anemi

    MCV & MCH

    transferring saturation total iron binding capacity

    ferrtitin

    iron reticulocytosis

    Investigation of cause Stool analysis worm or ova esinophilia female

    anclystoma hemoglobin infertility

    stool analysis worm or ova esinophilia

    51coloncopy

    Treatment Iron oral parentral ferrous sulphate & ferrous gluconate ferrous sulphate iron

    capsule iron acid iron Ferrous absorbtion

    acid gastric irritation gastritis

    acid stool dark stool malabsorbtion

    oral iron absorption 0mg

    rapid correction parentral iron

    parentral malabsorbtion rapid correction

    MCQ parentral and oral have the same rate of correction

    parentral IV ferrous iron acid iron

    ferrous acid IV ? vein vein

    thrombosis vein acid dilution vein thrombophlebitis

  • 10

    IM

    anclystoma mebendazole peptic ulcer proton pumb inhibitor

    Iron deficncey anemia

    Discuss Iron deficncey anemia

    anemia of chronic hemorrhage

    discuss anklystoma duednalis

    etiology

    chronic illness chronic infection- chronic inflammation- and malignancy

    chronic infection tb

    Inflammation : collagen disease

    Malignancy Tumor

    cytokines inflammatory mediators

    shortening life span of RBC 021.1

    cytokines suppression of BoneMarrow

    RBC suppression erythropoietin Kidney normocytic

    normochromic anemia

    iron release to the tissue iron transferritin

    BM Bone marrow Iron iron cytokines

    BM iron iron deficncy anemia iron serum

    iron

    anemia of choronic illness normochromic normocytic microcytic hypochromic

    Microcytic hypochromic inhibition of iron release to the tissue ferrritin

    iron deficny anemia investigation serum iron

    total binding capacity clinical picture iron ttt of underlying

    cause

    anemia of choronic illnessfailure to utilize iron cytokines iron

    iron

    sideroplastic anemia

    heme + globin heme iron and protoporphyrin

    Anemia of chronic illness

  • 11

    MCQ

    siderblastic anemia

    aminoacid glycine gamma amino levulinic acid

    1h :36

    synthesis Gamma amino levilunic synthetase enzyme VIT B6 folic acid

    sideroblastic anemia

    Not present * congenital

    VIt B 6 deficncy , folic acid deficncy INH VIT B6 metabolism

    lead poisiong inhibition protoporphyrin

    RBCs iron protoporphyrin siderblastic anemia

    - cases

    B12 Vit

    Sourceanimal source Vit B12

    Vb12 is only animal sources Oral stomach parietal cells intrinsic

    factor .. B12 terminal ileum absorbtion B12 blood

    transcobalamine -2 plasma Bone maroow RBCs CNSGIT

    excess Vit B12 liver 2 years

    under basal condition =D

    Function *

    b12 nucleas DNA cytoplasm cells division

    cytoplasm and nucleas double vit B12

    DNA

    B12 cytoplasm double

    Nucleas double divide

    divide megaloblasts

    bone marrow stem cells cells RBCs , WBCs

    and platlet cells proliferate B12 proliferate Megaloblasts

    anemia anemia

    bilirubin bilirubin cells Bone

    Sideroblastic anemia

    Vitamine B12 deficiency

  • 12

    marrow stage normoblast

    erythroblast

    at variable stage of development mature

    nucleas

    RBCs platelet thrombocytopenia WBCs

    enzyme serum muramidase

    immature multinucleated

    nucleas WBCs 3 lobes 6 lobes

    multilobated nuclueas

    Vit B 12 mylination of Nerve fibers

    GIT proliferate Vit B12

    proliferation

    etiology

    0 Diminshed intake

    Starvation, vegeterians vegetarian Egyptian vegetarian =D

    American vegetarian

    =D =D

    0 Diminshed intakeStarvationvegeterians ,

    2 diminished absorbtion

    intrinsic factor

    gatsrectomy, gastritis. Addissonian pernicious anemia automimmune disease

    Antibodis against parietal cells

    disease 0

    antibodies against parietal cells

    antibodies against intrinsic factor

    antibodies against terminal ileum

    ,high incidence against gastric carcinoma European female

    blue eye fair head females

    0 illeal disease

    2 infection , 2 inflammation , ,2

    2 infection ,TB & regional ileitis

    2 inflammaticrohns and ulcerative colitis

    2 blind loop syndrome Intestine peristalsis contents

    stagnant proliferation of bacteria

  • 13

    congenital Transcobalamine deficiency

    5 increase requirementpregnancy B12 malignancy

    cells proliferate V B12 hemolytic anemia bone marrow proliferating

    B12

    Clinical picture 0 FOG P

    2 specific jaundice hepatosplenomegaly purpra

    demylination sub acute combined degeneration red glaze tonge

    0 Cp of the cause

    Diminshed intake

    Addisoninan pernicious examination

    investigation

    nvestigationsI RBCs ESR

    Megaloblastic normochromic anemiaType

    MCV MCHC

    Specific nvestigations

    specific anisocytosis , poikilocytosis , cabbot rings

    High bilirubin serum LDH thrombocytopena mulitlobated WBCs muramidase

    No reticulcytes BM

    TTT reticulocytosis

    Inv of the cause

    endoscopy stomach

    perniciose anemia 0antibodies

    chilling testVit B12 Intestine obsolete

    Vit B12IM UGB12

    absorbtion urine urine

    intestine

    aborbtion urine test

    intrinsic factor intrinsic factor test

    B12antibiotic bacterial over growth

  • 14

    vit b 12

    underlying cause tb pernicious anemia HCL and pepsin

    Blood transfusion HB .HF

    Discuss vit b 12 deficency

    Discuss subacute combined degeneration

    discuss addisonian pernicious anemia

    source vegetables absorption intestine carrier

    inactive activation tetra hydro foliate GIT and

    bone marrow Vit B12 CNS liver

    0

    Etiology

    0 Deficient Intake anorexia and alcoholism

    2 Deficient absorbtion malabsorbtion syndrome drugs anticonvulsant anti epileptics

    0 Blood carrier dialysis dialysis b12

    carrier dialysis folic acid

    5 folic acid activation tetrahydrofolate drugs activation

    5 requirements malignancy , pregnancy and hemolytic anemia

    linical pictureCB12 CNS

    Investigations

    B12 chilling test FIGLU test absolete aminoacid

    Histidine H FIGLUFIGLU glutamic acid folic acid

    folic acid deficnecny Histidine FIGLU glutamic

    FIGLU Urine

    treatment

    folic acid

    underlying cause

    Folic acid MCQ B12

    Folic Acid deficiency

  • 15

    MCQ 151751=D

    =D

    Unipotent and pleuripotent

    Unipotent elementin one RBCs platelet and WBCs

    BM RBCS congenital diamond blackfan syndrome

    Thumb thumb0phalanges

    acquired Renal failure erythropoietein

    bronchogenic carcinoma or thymoma anti erythropoietin

    platlet wisckot Aldrich syndrome TAR

    syndrome

    .WBCs idiopathic

    Unipotent

    PleuripotentBM failure BM

    failure

    Idiopathic and drugs 61%

    idiopathiccorticosteroids

    autoimmune T B cells b cells

    antibodies T Cells T BM

    DrugsAntis anti emetic , antithyroid , antibiotic , antidiabetic

    infection , immunological, irradtion

    Infection tb and hepatitis

    Immunological SLE

    Infiltration leukemia and lymphoma

    Infiltration of BMmyetophthitic anemia

    chemicals benzene =D

    BM failure

    Clinical picture

    BM

    RBCs FOG P

    Bone marrow failure Aplastic anemia

  • 16

    platletbleeding tendency

    WBCs Infection already organismssevere up to septic shock

    CP of the cause

    investigations

    RBCs hematocrite ESR

    normocytic normochromic

    MCV & MCH normal

    Inv of the cause WBCs and platlets

    BM biopsy

    BM aspiration aspiration Under local anaesthia aspiration biopsy

    iliac crest aspiration fibrosis of bone

    marrow biopsy BM cavity fibrosis

    reatmentT RBCspacked RBCs

    platlets platlet

    WBCs anti fungal , antibiotic and antiviral WBCs =D WBCs

    antigen

    stimulate BM RBCs androgen or erythropoietin

    stimulate BM platlet danazol

    wbcs lithium side effects GCSF granulocyte

    stimulating factor

    idiopathic cyclosporine

    - MCQ 0.5

    S

    Hemolytic anemiashortening life span of RBCS RBCs Normal 210

    before 120 day this called hemolysis IF RBCs are destroyed

    rbcs 021hemolysis BM proliferate

    Replace damaged cells hemolysis

    .1BM replacement but no anemia

    60 replacement and no anemia

    40

    LIFE span 05bone marrow maximum capacity

    proliferate replacement replacement

    life span 05anemia 05021hemolysis only

    Hemolytic anemia

  • 17

    RBCs spleen and liver 65%extra vascular

    intravascular

    Extravascular 65%hemolytic anemia disease RBCs

    extravascular , disease intravascular hemolysis

    damage extravascularLiver and spleen

    disease RBCs extravascular hepatosplenomegaly RBCs

    anemia FOG P HT RBCs ESR

    RBCs LDH

    BM Bone marrow expansion Mongloid features

    XRay hair on end appearance wide medulla and thin cortex

    RBC s hemeoglobin heme + globin heme

    iron and protophorphyrin iron iron TIBC

    Transferring saturation iron

    tissue hemosiderosis CNS neuritis

    CVS cardiomyopathy

    abdomen

    liver liver cirrhosis

    lung interstitial lung fibrosis

    Kidney renal tubular disfunction

    genetalia endocrine damage testies , suprarenal and pituitary

    protoporphyrin biliverdin indirect bilirubin ID bilirubin

    cinically jaundice , gall bladder stones indirect urobilinogenurine

    stercobilinogen in stool

    disease extravscular hemolytic

    disease extravascularhepatosplenomegaly .. jaundice ,

    hemosidern inv RBCs HT ESR LDH

    stercobilinogen , urobilinogen 0

    extravascular

    extravascular 0

    Hematology

  • 18