Diagnostic Approach to Anemia Prof. Dr. Teoman SOYSAL.
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Transcript of Diagnostic Approach to Anemia Prof. Dr. Teoman SOYSAL.
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Diagnostic Approach to Anemia
Prof. Dr. Teoman SOYSAL
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Definition of anemia Anemia: A reduction in
– red cell mass
– O2-carrying capacity of blood It is expressed in terms of
reduction in the concentration of Hb (or RBC or Hct%) compared to values obtained from a reference population.
(2 SD below normal)
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Reference values (adults) (I)
Parameter Female Male RBC (x1012/L) 4.8+0.6
5.4+0.9 Hb (g/dL) 14+2 16+2 Htc (%) 42+5 47+5
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Definition of anemia Hb level of a patient which is below the
normal ranges of that age and sex. For adults:
WHO criteria define anemia as – hemoglobin
<12 g/dL in women and <13 g/dL in men
But: The reference values for red cells ,Hb or Hct may difer according to – sex/age– Race– Altitude– Socioeconomical changes– Study/reference etc
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BEUTLER andWAALEN BLOOD, 1 MARCH 2006 VOLUME 107, NUMBER 5
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age WBC Neutrophyls Eos. Baso Lenfo Mono Hb
12 mo 6-17.5 1.5-8.5 0.05-0.7 0-0.20 4-10.5 0.05-1.1 11.1-14.1
4 y 5.5-15 1.5-8.5 0.02-0.65
0-0.20 2-8 0-0.8 11.2-14.3
6 y 5-14.5 1.5-8 0-0.65 0-0.20 1.5-7 0-0.8 11.4-14.5
10 y 4.5-13 1.8-8 0-0.60 0-0.20 1.5-6.5 0-0.8 11.8-15
21 y 4.5-11 1.8-7.7 0-0.45 0-0.20 1-4.8 0-0.8 E: 16K: 14
WBC: x10E3/mm3 Hb:g/dL
Age and blood count changes
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Reference values (II)
Ret (% / n) 0.5-2.5 / 50-100x109/L MCV (fl) 90+7
MCH (pg) 29+2
MCHc (g/dL) 34+2
RDW (%) 11.5-14.5
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50 100 200 fl
RBC
%
50 100 200 fl
RBC
%
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50 100 200 fl
RBC
%RDW: Red cell distribution width
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50 100 200 fl
RBC
%
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Reticulocyte
Normal Ranges Male: % 0.8 - 2.5 Female: % 0.8 - 4.1
Corrected Rtc: Patient Hb/Normal Hb x Rtc
%
Reticulocytosis: > 100.000 /mm3
Increased counts• Hemolysis• Acute bleeding• Response to
treatment
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Diagnosis and investigation:
Is the patient anemic? What is the type of anemia? What is the cause of anemia?
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Classification of anemia Morphologic
– Normocytic: MCV= 80-100fL– Macrocytic: MCV > 100 fL– Microcytic : MCV < 80 fL
Pathogenic (underlying mechanism)– Blood loss (bleeding)– Decreased RBC production– Increased RBC destruction/pooling
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!!!!!
Plasma volume changes have to be considered before determining a diagnosis of anemia .– Volume contraction:Underestimation of
anemia– Volume overload: Underestimation of Hb
level
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Volume changes/acute bleeding
and anemia
normal
Hct:Normal
Dehydration Hct:Increased
Acute blood loss(early) Hct:unchanged
Chronic anemia Hct: Low
1 2 3 4 5
Increased plasma volume Hct: Low
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!!!!!
A normal Hb in a patient in whom an elevated Hb level is expected may represent anemia .(eg:COPD + Hb:N)
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!!!!!!
Different red cell measures of a patient may give discordant values in special conditions.
eg:Thalassemia trait Low Hb, high RBC, low MCV,normal RDW
Hb: 10 g/dL (anemia) RBC: 6.5 million/mm3
(erythrocytosis) MVC : 65 fL RDW: Normal
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!!!!
Anemia is rarely a disease by itself,
It is mostly a manifestation or consequence of an underlying (genetic or acquired) disease.
The finding of anemia has to start attempts to disclose an underlying disease . – What is the cause of anemia ?
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Normocytic Anemias
Acute post-hemorrhagic anemia Hemolytic anemia (except thalassemia and
some other Hb disorders) Aplastic anemia Pure red cell aplasia Bone marrow infiltration
Endocrin diseases Renal failure Liver disease Chronic disease anemia Protein malnutrition Hypovitaminosis C
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Microcytic anemias
Iron deficiency anemia Thalassemia Sideroblastic anemia Lead poisoning Anemia of chronic diseases (some cases)
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Macrocytic anemias
Megaloblastic– Oval macrocytes
Non-megaloblastic
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Megaloblastic Macrocytic Anemias
Vit B12 deficiency Folic acid deficiency Other.
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Non-megaloblastic Macrocytic Anemias
Anemia of acute bleeding Hemolytic anemias Leukemias (esp: acute) Myelodysplastic syndromes Liver disease
Aplastic anemia Diseases infiltrative to the bone
marrow Alcoholism Hypothyroidism Scurvy
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Pathogenic classification(Causes of anemia)
Relative (increased plasma volume) Decreased RBC production Blood loss
– Anemia due to acute bleeding Increased RBC destruction
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Pathogenic classification(Causes of anemia)
Decreased RBC production– Decreased Hb production– Defective DNA synthesis– Stem cell defects
Pluripotent stem cell Erythroid stem cell(progenitors)
– Other less defined reasons Blood loss
– Anemia due to acute bleeding Increased RBC destruction Relative(increased plasma volume)
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Decreased Hb production Iron deficiency anemia Thalassemia Sideroblastic anemia Lead poisoning
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Defective DNA synthesis
Vit B12 deficiency Folic acid deficiency Other.
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Pluripotent stem cell defects
Aplastic anemia Leukemia or myelodysplastic syndromes
Defective erythroid stem cell
Pure red cell aplasia Anemia of chronic renal failure Endocrin disease anemia Congenital dyserythropoetic anemias
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Decreased RBC production due to multipl or undefined mechanisms
Anemia of chronic diseases Bone marrow infiltration Anemia due to nutritional defects
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Anemias caused by increased RBC destruction (hemolytic anemias) Can be classified as; Hemolysis due to intracorpuscular
defects Hemolysis due to extracorpuscular
defectsOr Hereditary hemolytic diseases Acquired hem. diseasesOr Intravascular hemolysis Extravascular hemolysis etc.
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1- Abnormalities of RBC interior
a. Enzyme defects
b. Hemoglobinopathies & Thalassemia M
2-RBC membrane abnormalities
a. Hereditary spherocytosis, elliptocytosis etc b. Paroxysmal nocturnal hemoglobinuria c. Spur cell anemia
3- Extrinsic factors
a. Hypersplenism b. Antibody : immune hemolysis c. Traumatic & Microangiopathic hemolysis d. Infections , toxins , etc
Intr
acor
pu
scu
lar
Ext
raco
rpu
scu
lar
Hereditary
Acquired
A Very Simple Classification of Hemolytic Anemias
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Is the patient anemic ?
RBC count HB level Hct level Volume status
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What is the type of anemia? History and physical exam. RBC,HB,Hct , MCV, MCH,RDW Red cell morphology ( peripheral
smear) Reticulocyte count
– Incresed ? Other Lab. investigations
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Lab. investigation of anemia(1)
WBC count and differential Platelet count and morphology ESR Biochemistry, special tests and
others Bone marrow exam.(only when
indicated)
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Lab. investigation of anemia(2)
Serum values of– Iron– TIBC– Ferritin– Bilirubins– Proteins / electrophoresis– LDH– Vit B12 and /or Folic acid(None of these tests are routine screening
tests)
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Lab. Investigation of Anemia(3)
Liver, renal, endocrin functional tests Urinalysis
– Hemosiderin Occult GIS bleeding / parasites etc(tests should be chosen individually-do not order routinly ) Tests to diagnose the type of hemolytic
anemia– If hemolytic anemia is considered
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Normocytic anemia
Retic. count normal/low
Secondary anemia
Renal, Hepatic, Endocrin , Chronic
disease(Normal marrow)
Hypoplastic Marrow
AA, pure red cell aplasia
Bone marrow infiltrative diseases
Leukemia , Myelofibrosis
Metastatic disease
Dysplastic marrow:
MDS
Retic. count increased
Response to treatment
Hemolytic anemia
Acute bleeding
• No sign of secondary anemia
• Other signs of bone marrow disease may be +
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Microcytic anemia
Serum iron high
Bone marrow iron content
and sideroblasts
Sideroblastic anemia
Serum iron normal /high
Hemoglobin studies
Thalassemia , HbC , others
Serum iron decreased
Ferritin low
Iron deficiency
Ferritin: Normal or increased
Anemia of chronic
diseases
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Macrocytic anemia
Peripheral smearRetic. count
Retic. count Increased
HemolysisAcute
bleeding
Retic. count Normal/
decreased
Megaloblastic
Deficiencies of VitB12 ,Folic acid or other
causes
Non-MegaloblasticLiver diseases
Myelodysplastic syndrome
Bone marrow infiltrationAcute leukemia
Aplastic Anemia,Alcoholism
Hypothyoidism etc
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Case I 38 years old, ♀ Tiredness, hair loss, nail changes
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Microcytic anemia
Serum iron high
Bone marrow iron content
and sideroblasts
Sideroblastic anemia
Serum iron normal /high
Hemoglobin studies
Thalassemia , HbC , others
Serum iron decreased
Ferritin low
Iron deficiency
Ferritin: Normal or increased
Anemia of chronic
diseases
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Microcytic anemiasDiagnosis(type of anemia)
MCV RDW Serum Iron
Iron binding capacity
Ferritin
ESR/acute phase signs
Hemogl. changes
Iron deficiency
May change None
Thalassemia N N Normal
May be diagnostic
Chronic disease anemia
N Elevated None
RBC count:Thalassemia minor >Iron deficiency
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Case I 38 years old, ♀ Tiredness, hair loss, nail changes
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What is your diagnosis?
What is the next step?– Prove iron deficiency
Serum iron, TIBC, Ferritin– Find out the cause of iron deficiency
Chronic blood loss / excessive need-inadequate intake
– Menstruel bleeding, Pregnancy – GI bleeding– Inadequate intake or malabsorbtion etc
– Treat both iron deficiency and the cause
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Case II26 y oSlight symptoms• Decreased
excercise tolerence
• Paleness• Long history of
being anemic on routine CBC’s ,non responsive to iron
RBC:5.500.000/mm3
Hb: 10 g/dLMCV: 60 fLRDW: 14.3Retic: %2WBC: 5000/mm3
Plt: 200.000/mm3
Name the blood picture.Further questions to ask to the patient?Further tests to do ?Ferritin : slightly elevatedHbA2: slightly elevated, Hb F: normalFinal Diagnosis ?
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Case III• 70 y o, male• Fatigue, weakness• Sore tongue, poor taste
sensation• Papill. atrophy-beefy tongue• Paresthesias• Loss of position sense, ataxia• Decreased deep tendon
reflexes
3 units of red cell transfusion made before admission
Macrocytosis Anisocytosis, neutrophyl hypersegmentation, oval macrocytes
WBC: 2.300/µl Hgb: 11 g/dLHct: %33MCV: 122 fLMCH: 39pgMCHC: %34RDW: 30.5Plt: 100.000/µlRetic: 1%
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Macrocytic anemia
Peripheral smearRetic. count
Retic. count Increased
HemolysisAcute bleeding
Retic. count Normal/
decreased
Megaloblastic
Deficiencies of
VitB12 ,Folic acid
or other causes
Non-Megaloblastic
Liver diseasesMyelodysplastic
syndromeBone marrow infiltration
Acute leukemiaAplastic Anemia,
Alcoholism Hypothyoidism etc
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What is the blood picture ?(The type of the disorder) What is your diagnosis?
– Why?
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Normocytic anemia
Retic. count normal/low
Secondary anemia
Renal, Hepatic, Endocrin , Chronic
disease(Normal marrow)
Hypoplastic Marrow
AA, pure red cell aplasia
Bone marrow infiltrative diseases
Leukemia , Myelofibrosis
Metastatic disease
Dysplastic marrow:
MDS
Retic. count increased
Response to treatment
Hemolytic anemia
Acute bleeding
• No sign of secondary anemia
• Other signs of bone marrow disease may be +
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60 y o Normocytic anemiaReticulocytes: 1%
Pale, pruritus, hypertensionUrea + creatinin elevated
Hoarse voiceLethargyHair lossDry skinWeight gainPoor memoryBradycardia
?
?
Symmetric polyarthritisMorning stiffnessSc nodules
?
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Normocytic anemia, MCV normal, RDW ↑,
Case IV• 65 y o , male• One month history of fever, cough and hemoptysis• ESR: 80mm/h; high CRP• Sputum + for TBC bacteria; chest x-ray shows right apical infiltrate
What is the type of anemia?
What is the diagnosis?
• This case could also present as a
microcytic anemia .What would
you expect from the iron studies
in that situation?
Low iron, Low TIBC, High
Ferritin
Retic.: 2%
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Normocytic anemia
Retic. count normal/low
Secondary anemia
Renal, Hepatic, Endocrin , Chronic
disease(Normal marrow)
Hypoplastic Marrow
AA, pure red cell aplasia
Bone marrow infiltrative diseases
Leukemia , Myelofibrosis
Metastatic disease
Dysplastic marrow:
MDS
Retic. count increased
Response to treatment
Hemolytic anemia
How to decide the next step?
HistoryPE
SmearOther tests
Acute bleeding
• No sign of secondary anemia
• Other signs of bone marrow disease
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Case IX
67 y o, male• Anemia
symptoms• Severe bone
painCBC• Normocytic
anemia
What is your possible diagnosis?What is the next step?
• ESR:>100mm/h• Hypercalcemia• Hyperglobulinem
ia• Renal failure
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Morphologic abnormalities in hemolytic anemias
• Sickle cell:
• Target cels:
• Schistocytes:
• Agglutination:
• Heinz bodies:
Sickle cell anemia
Thalassemia, HbC disease, liver disease,
splenectomy
Microangiopathic hem anemia, uremia, DIC,
malignant hypertesion, eclampsia,
disseminated vasculitis or malignancy,
Cold agglutinin disease
Unstable Hb, G6PD deficiency and oxidant stress
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Special Lab. Examinations
Coombs antiglobulin test - immune hemolysis Osmotic fragility test - spherocytosis Autohemolysis- G6PD,PK, spherocytosis Red cell enzyme assays- RBC enzyme defects Membrane protein analysis- membrane defects Red cell sickling, HbS- sickle cell anemia Hemoglobin electrophoresis and HbA2, Hb F ,
HHb,etc - Hemoglobinopathies and thalassemias HAM and sucrose lysis tests and GPI-linked protein
analysis by flow cytometry- PNH Oxygen dissociation curve- High oxygen affinity
Hb
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Case V
18 y o , maleWeakness, paleness, slight icterus, splenomegaly, bile stonesFamily history +WBC: 5600/µl Hgb: 9,6 g/dLMCHC: %37Plt: 300.000/µl Retic: %9
spherocyte
Normal RBC
Ind Bil: slightly elevatedLDH: elevatedHaptoglobin : lowRed cell osmotic fragility increased
?
?
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Case VI38 y o Cough , fever
WBC: 12.000/µl Hgb: 11 g/dL Hct: 22 %MCV: 130 MCH: 40 MCHC: 36RDW:28Plt: 160.000/µl
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Case VII
34 y o, male2-3 weeks history of• Decreased exercise
capacity• Paleness• Headache, sore throat2 days history of • Cough and fever• Red spots on the skin
CBCWBC: 33.000/mm3
Hb: 7 g/dLRetic: 1%Plt: 12.000/mm3
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Case IX60 y o, femaleSudden onset
Pallor, palpitationSlight scleral icterussplenomegaly
CBC Hb: 8 g/dL WBC: 10.000/mm3 Plt: 450.000/mm3 Retic: 10%
What is your diagnosis?What is your next step?
Indirect bilirubin: highLDH: highHaptoglobin: lowD/I: Coombs +
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Case X
70 y o , male• Under examination
for prostat enlargement
+One month history of• Bone pain• Symptoms of anemiaWBC: 8000/mm3Hb: 8 g/dLMCV: 88 fLRDW: 14Retic: 2%Plt: 220.000/mm3
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Morphologic abnormalities in hemolytic anemias
Polychromasia:
Spherocyte :
Elliptocytes: Stomatocytes
: Acanthocytes
:
Echinocytes:
Reticulocytes
Hereditary spherocytosis, immune hem. anemia,
burns, chemical injury to RBC
Hereditary ovalocytosis,
Hereditary stomatocytosis, alcoholism
Spur cell anemia with liver disease,
abetalipoproteinemia
Pyruvate kinase deficiency, uremia