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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
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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
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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 ,
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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