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Premium member Presentation Transcript UNIT 3 ANEMIA And Its Laboratory Diagnosis : 1 UNIT 3 ANEMIA And Its Laboratory Diagnosis By: Bamlaku Enawgaw university of Gondar, GCMHS, MLS firstname.lastname@example.org +251 913 15 02 39Objectives: 2 Objectives At the end of this chapter you will be able to: Define anemia Discuss the causes and clinical significance of different categories of anemia Describe the classification of anemia Explain - Microcytic anemia - Macrocytic anemia - Normochromic normocytic anemia Discuss the laboratory findings for each category of anemia Perform basic laboratory tests for the diagnosis of anemiaChapter Outline: 3 Chapter Outline 3.1. Definition of anemias 3.2. Classification of anemias 3.2.1. Hematologic Response to Anemia 3.2.2. Signs of Accelerated Bone Marrow Erythropoiesis 3.2.3. Physiologic Response to Anemia 3.2.4. Methods of classification 3.2.5. Anemia Diagnosis/Cause 3.2.6. Lab Investigation of Anemia 3.3. Types of anemia . 3.3.1 microcytic hypochromic anemia 3.3.2. macrocytic normocytic anemias 3.3.3. normocytic anemias 3.3.4. normocytic anemias due to hemoglobinopathies3.1. Introduction : 4 3.1. Introduction 3.1.1. Definition of Anemia Anemia is a decrease in the RBC count, Hgb and/or HCT values as compared to normal reference range for age and sex (Also determined by alteration in plasma volume) ‘True’ anemia: decreased RBC mass and normal plasma volume Pseudo or dilutional anemia: normal RBC mass and increased plasma volume An increase in plasma volume can occur in Pregnancy, volume overload (IVs) congestive heart failure Low Hgb and HCT valuesDefinition of Anemia cont’d: 5 Definition of Anemia cont’d3.1.1. Definition of Anemia cont’d…..: 6 3.1.1. Definition of Anemia cont’d….. Anemia must also relate to the level of hemoglobin the individual normally possesses. If an adult male usually maintains a hemoglobin level of 16g/dl, and over a period of days is noted to have decreased to 14g/dl, this must be considered significant even though both values are within the normal range for an adult male.3.1.1. Definition of Anemia cont’d…..: 7 3.1.1. Definition of Anemia cont’d….. Various diseases and disorders are associated with decreased hemoglobin levels. These include: Nutritional deficiencies External or internal blood loss Increased destruction of RBCs Ineffective or decreased production of RBCs Abnormal hemoglobin synthesis Bone marrow suppression by toxins, chemicals, or radiation replacement by malignant cells Infection3.1.1. Definition of Anemia cont’d…..: 8 3.1.1. Definition of Anemia cont’d….. Functionally anemia is defined as tissue hypoxia (inability of the body to supply tissue with adequate oxygen for proper metabolic function) There is an abnormal hemoglobin with an increased O 2 affinity resulting in an anemia with normal or raised hemoglobin levels, hematocrit, or RBC count. Generally anemia is not a disease, but rather the expression of an underlying disorder or disease.3.1.1. Definition of Anemia cont’d…..: 9 3.1.1. Definition of Anemia cont’d….. Anemia may develop: When RBC loss or destruction exceeds the maximal capacity of bone marrow RBC production or When bone marrow production is impaired3.1.2.Hematologic Response to Anemia: 10 3.1.2.Hematologic Response to Anemia Tissue hypoxia causes increased renal release of erythropoietin (EPO) to accelerate bone marrow erythropoiesis The normal bone marrow can increase its activity 7-8 times normal Marrow becomes hypercellularSigns of Accelerated Bone Marrow Erythropoiesis: 11 Signs of Accelerated Bone Marrow Erythropoiesis The marrow becomes hypercellular due to a marked increase in RBC precursors (called erythroid hyperplasia) and the M:E ratio falls. Nucleated RBCs may be released into the blood circulation along with the outpouring of reticulocytes NRBC number tends to correlate with the severity of anemia I ncreased polychromasia on the Wright's- stained blood smear is seen due to increased number of circulating Retics.Slide 12: 12 If demand exceeds maximal bone marrow activity, RBC production may occur in extramedullary sites, liver, spleen (hepatosplenomegaly).3.1.3. Physiologic Response to Anemia: 13 3.1.3. Physiologic Response to Anemia Ability to adapt to anemia depends on: Age and underlying disease Cardio/pulmonary function Rate at which anemia develops (BM can compensate easier if the onset of anemia is slow), Underlying disease3.1.4. Clinical features: : 14 3.1.4. Clinical features: Symptoms of hypoxia : decreased oxygen delivery to the tissues/organs causes: fatigue , faintness, weakness, dizziness, headaches, dyspnea, poor exercise tolerance, leg cramps.Slide 15: 15 Signs of anemia general signs include pallor of mucous membrane, which occur if the Hgb concentration is less than 9g/dl, specific signs are associated with particular types of anemia, for example, jaundice in hemolytic anemia, leg ulcer in sickle cell anemia 3.1.4.Clinical features cont’d….:3.1.5. Diagnosis of anemia: 16 3.1.5. Diagnosis of anemia Before making a diagnosis of anemia, one must consider: Age Sex Geographic location Presence or absence of lung disease3.1.5. Diagnosis of anemia cont’d……: 17 3.1.5. Diagnosis of anemia cont’d…… How does one make a clinical diagnosis of anemia? A. Patient history Dietary habits Medication Possible exposure to chemicals and/or toxins Description and duration of symptoms3.1.5. Diagnosis of anemia cont’d……: 18 3.1.5. Diagnosis of anemia cont’d…… Tiredness Muscle fatigue and weakness Headache and vertigo (dizziness) Dyspnia (difficult or labored breathing) from exertion G I problems Overt signs of blood loss such as hematuria (blood in urine) or black stools Patient history cont ………..3.1.5. Diagnosis of anemia cont’d….: 19 3.1.5. Diagnosis of anemia cont’d…. B . Physical exam General findings Hepato or splenomegaly Heart abnormalities Skin pallor Specific findings In vitamin B 12 deficiency there may be signs of malnutrition and neurological changes In iron deficiency there may be severe pallor, a smooth tongue, and esophageal webs In hemolytic anemias there may be jaundice due to the increased levels of bilirubin from increased RBC destruction3.1.5. Diagnosis of anemia cont’d……: 20 3.1.5. Diagnosis of anemia cont’d…… C. Lab investigations A complete blood count, CBC RBC count Hematocrit (Hct) or packed cell volume Hemoglobin determination RBC indices calculation Reticulocyte count Blood smear examination to evaluate: Poikilocytosis Leukocytes or Platelets abnormalities3.1.5. Diagnosis of anemia cont’d…..: 21 3.1.5. Diagnosis of anemia cont’d….. Lab investigation cont’d…… A bone marrow smear and biopsy to observe: Maturation of RBC and WBC series Ratio of myeloid to erythroid series Abundance of iron stores (ringed sideroblasts) Presence or absence of granulomas or tumor cells Red to yellow ratio Presence of megakaryocytes4. Hemoglobin electrophoresis: 22 4. Hemoglobin electrophoresis 3.1.5. Diagnosis of anemia cont’d …..3.1.5. Diagnosis of anemia cont’d…..: 23 3.1.5. Diagnosis of anemia cont’d….. Lab investigation cont’d…… 5. Antiglobulin testing 6. Osmotic fragility test3.2. Methods of Anemia Classification: 24 3.2. Methods of Anemia Classification Several schemes of classifying anemias exist Morphologic Based on RBC morphology Anemia is divided into three groups mainly on the basis of the MCV (RBC indices) Pathophysiologic Anemia is divided using three main causes/mechanisms Impaired erythrocyte formation (Aplastic anemia, IDA, sideroblastic anemia, anemia of chronic diseases, megaloblastic anemia) Retic count is low The bone marrow fails to respond appropriately due to disease or lack of essential suppliesMethods of Classification cont’d: 25 Methods of Classification cont’d Increased blood loss (Acute, Chronic) Retic count is typically high Anemia results when red cell loss exceeds the bone marrow’s capacity to increase its activity Increased destruction of RBCs (hemolytic anemias) Retic count is typically high Anemia results when red cell destruction exceeds the bone marrow’s capacity to increase its activityMethods of Classification cont’d: 26 Methods of Classification cont’d Morphologic Categories of Anemia Normocytic Normochromic anemia (normal red cell indices) Blood loss anemia Hemolytic anemia Aplastic anemia Chronic diseaes Renal insufficciencySlide 27: 27 Morphologic Categories of Anemia Microcytic hypochromic ( low red cell indices) Iron deficiency anemia Sideroblastic anemia Lead poisoning Thallassemia Chronic diseases Methods of Classification cont’dSlide 28: 28 Morphologic Categories of Anemia Macrocytic Normochromic ( high MCV and MCH, normal MCHC) Megaloblastic anemia Liver disease Post splenectomy Hypothyroidism Stress erythropoiesis Methods of Classification cont’dMorphologic Categories of Anemia: 29 1 Microcytic/hypochromic 3 1 2 2 Macrocytic/Normochromic 3 Normocytic/Normochromic Morphologic Categories of Anemia N.B. The nucleus of a small lymphocyte (shown by the arrow) is used as a reference to a normal red cell size3.2.2. Pathophysiological classification: 30 3.2.2. Pathophysiological classification 1. B. 2. A.1. Microcytic- Hypochromic Anemia: 31 1. Microcytic- Hypochromic AnemiaMicrocytic- Hypochromic Anemia: 32 Microcytic- Hypochromic Anemia Many RBCs smaller than nucleus of normal lymphocytes Increased central pallor. Includes Iron deficiency anemia Thalassemia Anemia of chronic disease Sideroblastic anemia Lead poisoningSlide 33: 33 Iron Protoporphyrin Heme Globin + Hemoglobin Iron deficiency Chronic inflammation or malignant (ACD) Thalassemia ( or ) Sideroblastic anemia The Cause of Microcytic- Hypochromic AnemiaMicrocytic/Hypochromic Anemias: 34 RBC maturation in microcytic anemias Normoblastic RBC maturation normocytic red cells Abbott Manual Microcytic/Hypochromic Anemias Normal RBC maturation is shown for comparisonA. Iron Deficiency Anemia (IDA) : 35 A. Iron Deficiency Anemia (IDA) Is a condition in which the total body iron content is decreased below a normal level This results in a reduced red blood cell and hemoglobin production More than half of all anemias are due to iron deficiency.Iron Deficiency Anemia (IDA): 36 Iron Deficiency Anemia (IDA) Causes: Nutritional deficiency Malabsorption (insufficient or defective absorption) Inefficient transport, storage or utilization of iron Increased need Chronic blood loss (GI bleeding, ulcer, heavy menstruation, etc)DIETARY SOURCES OF IRON: 37 DIETARY SOURCES OF IRON Inorganic Iron eg lentils Organic iron eg beef DAILY IRON REQUIREMENT 10-15mg/day (5-10% absorbed)Daily Iron cycle (Fig): 38 Daily Iron cycle (Fig)Slide 39: 39 Adult men 0.5-1 Post menopausal female 0.5-1 Menstruating female 1-2 Pregnant female 1.5-3 Children 1.1 Female (age 12-15) 1.6-2.6 Estimated daily iron requirements Units are mg/dayIron absorption, Transport and storage: 40 Iron absorption, Transport and storage Iron absorbed from duodenum and jejunum in the GIT Moves via circulation to the bone marrow Incorporated with protoporpyirin in mitochondria of the erythroid precursor to make HemeSlide 41: 41 There are three proteins important for transporting and storage of iron: Transferrin, Transferrin receptors and Ferritin Transport: Transferrin: transports iron from the plasma to the erythroblasts in the marrow for erythropoiesis The transferrin will bind to transferrin receptor on the erythrocyte membraneSlide 42: 42 Storage Hgb contains about two third of the body iron At the end of their life, RBCs are broken down in the macrophage of reticuloendothelial system and then iron is released from Hgb enters plasma and provided to transferrin. Some stored in reticuloendothelial cell as ferritin soluble protein – iron complex) and hemosiderin (37%) (degraded form of ferritin insoluble) iron is also found in muscles as myoglobin and in other cells as iron containing enzymesSlide 43: 43 Amount of iron Male Female % in average adult (g) (g) of total Hb 2.4 1.7 65 ferritin & hemosiderin 1.0 0.3 30 Myoglobin 0.15 0.12 3.5 Heme enzyme 0.02 0.15 0.5 Transferrin-bound 0.004 0.003 0.1 iron The distribution of body ironIron Deficiency Anemia (IDA) : 44 Iron Deficiency Anemia (IDA) Sequence of iron depletion When iron loss or use exceeds absorption, there is a sequence of iron depletion in the body: Storage iron decreases/ low serum ferritin ; serum iron & TIBC are normal, no anemia, normal red cells. Serum iron decreases/TIBC increases (increased transferrin); no anemia, normal red cells. Anemia with microcytic/hypochromic red cells = IDA.CLINICAL FEATURES IRON DEFICIENCY: 45 CLINICAL FEATURES IRON DEFICIENCY Symptoms eg. fatigue, dizziness, headache Signs eg. pallor, Tongue atrophy/ glossitis - raw and sore , angular cheilosis (Stomatitis) Koilonychia Glossitis Angular Cheilosis or StomatitisSlide 46: 46 Clinical signs and symptoms Spoon‑shaped nails (koilonychia), brittle nails and hair.Lab Investigation of IDA: 47 Lab Investigation of IDA Iron tests ► Used to differentiate microcytic hypochromic anemia's or detect iron overload ( hemochromatosis) Iron circulates bound to the transport protein transferrin Transferrin is normally ~33% saturated with iron Iron tests include serum iron, Total Iron Binding Capacity (TIBC), serum ferritinLab Investigation cont’d: 48 Lab Investigation cont’d Serum iron level measures the amount of iron bound to transferrin Does not include the free form of iron Total Iron Binding Capacity (TIBC) Is an indirect measure of the amount of transferrin protein in the serum Inversely proportional to the serum iron level If serum iron is decreased, total iron binding capacity of transferrin increased (transferrin has more empty space to carry iron)Lab Investigation cont’d: 49 Lab Investigation cont’d Serum ferritin indirectly reflects storage iron in tissues found in trace amount in plasma It is in equilibrium with the body stores Variation in the quantity of iron in the storing compartment is reflected by plasma ferritin concentration e.g. Plasma ferritin is decreases in IDA Plasma ferritin increases in ACD Limitation: D uring infection or inflammation Serum Ferritin increases like other acute phase proteins, and then it is not an accurate indicator in such situations.Bone marrow iron (Tissue iron): 50 Bone marrow iron (Tissue iron) Tissue biopsy of bone marrow Prussian blue stain Type of iron is hemosiderinSlide 51: 51 ABSENT IRON STORES IN BONE MARROW IN IRON DEFICIENCY Iron deficiency Normal controlIron Deficiency Anemia: 52 Iron Deficiency Anemia Lab findings Low RBC, Hgb, Hct Low MCV, MCH, MCHC Normal WBC and PLT Blood smearIron Deficiency Anemia: 53 Iron Deficiency Anemia RBC morphology Hypochromia Microcytosis Anisocytosis Poikilocytosis Pencil cells (cigar cells) Target cells no RBC inclusions Iron parameters Low serum iron, High TIBC, Low serum ferritin Blood smearIron Deficiency: 54 Wright’s stained blood smear Ovalocytes - Pencil forms No RBC inclusions Iron DeficiencyIDA cont’d: 55 IDA cont’d Treatment Identify the underlying cause Oral iron is given; see increased Retic count post-therapy. May see dimorphism following treatment a dual red cell population with older microcytic red cells along with the newly produced normocytic red cells.B. Sideroblastic Anemia (SA): 56 B. Sideroblastic Anemia (SA) This group of anemias are characterized by defective protoporphyrin synthesis (blocks) resulting in iron loading and a hypochromic anemia due to deficient hemoglobin synthesis. Block(s) in protoporphyrin synthesis leads to iron overload and microcytic/hypochromic anemiaSideroblastic Anemia (SA): 57 Sideroblastic Anemia (SA)Terms: : 58 Terms: Siderocytes are mature RBCs in the blood containing iron granules called Pappenheimer bodies.... abnormal. Sideroblasts are immature nucleated RBCs in the bone marrow containing small amounts of iron in the cytoplasm .... normal.SA: 59 SA Sideroblastic anemia is characterized by the Accumulation of iron in the mitochondria of immature nucleated RBCs in the bone marrow; Iron forms a ring around the nucleus these are called ringed sideroblasts ....abnormal. The iron accumulation in the mitochondria is the result of blocks in the protoporphyrin pathway .SA cont’d: 60 SA cont’d Lab findings: Microcytic/hypochromic red cells, low MCV and MCHC; variable anemia, low retic. RBC inclusions: Basophilic stippling and Pappenheimer bodies (siderocytes). (May see target cells). High serum iron and high serum ferritin (stores); low TIBC and high % saturation. * Decreased transferrin synthesis occurs in iron overload states. Bone marrow: ringed syderoblasts (Hall mark of Sideroblastic Anemia)Sideroblastic Anemia (SA): 61 61 RBC with iron Wright’s stain NRBC with iron Prussian blue stain NRBC with ring of iron Prussian blue stain Pappenheimer bodies Blood Bone marrow Bone marrow Sideroblast Ringed Sideroblast Sideroblastic Anemia (SA)Sideroblastic Anemia (SA): 62 Pappenheimer bodies Wright’s stain Blood Basophilic stippling/stippled RBCs Blood Pappenheimer bodies Prussian blue iron stain Blood Sideroblastic Anemia (SA)Sideroblastic Anemia (SA) Bone marrow findings (if done):: 63 100x Ringed Sideroblasts Prussian blue iron stain Bone marrow 10x Increased stainable iron Prussian blue iron stain Bone marrow Sideroblastic Anemia (SA) Bone marrow findings (if done): *Ringed sideroblasts demonstrated with Prussian blue stain. Increased stainable iron in macrophages.Types of Sideroblastic anemia cont’d : 64 Types of Sideroblastic anemia cont’d Primary ‑ cause unknown (can't identify blocks) and are not reversible ....called Idiopathic or primary Sideroblastic anemia. Elderly, responds to no treatment. Requires transfusion support if severe anemia. Characterized by a dimorphic red cell population - micro/hypo red cells with normocytic and/or macrocytic red cells....MCV is variable and RDW is high. Primary type of sideroblastic anemia is one of myelodysplastic syndromes called Refractory Anemia with Ringed Sideroblasts; may terminate in leukemiaSecondary Types of SA: 65 Wright’s stained blood smear Stippled RBCs – Lead poisoning Secondary Types of SA Alcohol inhibits vitamin B6/pyridoxine Anti-tuberculosis drugs inhibit vitamin B6 Lead causes multiple blocks Inhaled or ingested Abnormal lead level Neurologic problems Lead line (gums) Chelation therapy (EDTA).Slide 66: 66C. Anemia of chronic disease: 67 C. Anemia of chronic disease Anemia of chronic disease (ACD) – inability to use iron and decreased response to EPO Very common anemia, #2 Associated with systemic disease, including chronic inflammatory conditions: Rheumatoid arthritis Chronic renal disease Thyroid disease Malignancies Tuberculosis Chronic fungal infections etcACD pathogenesis: 68 ACD pathogenesis Lactoferrin is an iron biding protein in the granules of neutrophils Its avidity for iron is grater than transferrin During infection or Inflammation, neutrophil-lactoferrin released into plasma and Scavenges available iron Bind to macrophage and liver cells (because they have receptor for lactoferrin Cytokines: Produced by macrophages during inflammation and contribute to ACD by inhibiting erythropoiesisLab Diagnosis: 69 Lab Diagnosis Blood findings Early stage: normocytic normochromic Late stage: hypochromic microcytic, Low serum iron, low TIBC, normal or high serum ferritin Leukocytosis Abundant storage of iron in macrophage (Prusian blue)D. Thalassemias : 70 70 Target cells/Codocytes Beta Alpha D. Thalassemias Inherited decrease in alpha or beta globin chain synthesis needed for Hgb A; quantitative defect All have microcytic/hypochromic RBCs and target cells Genetic mutations classified by: ↓ beta chains = beta thalassemia…Greek/Italian ↓ alpha chains = alpha thalassemia…AsianSlide 71: 71 Haemoglobin Molecule Hgb A = 2 α & 2 β Hgb A 2 = 2 α & 2 δ Hgb F = 2 α & 2 γ Consists of 4 globin chains + 4 heme groups Normally , each individual inherits 2α, 1β, 1γ, and 1δ gene from each parent.....so 4α, 2β, 2γ, and 2δ genes are inherited. 97% 2% 1%Thalassemia : 72 Thalassemia Impaired alpha or beta globin synthesis results in an unbalanced number of chains produced that leads to: RBC destruction in beta Thalassemia major Production of compensatory Hgb types in beta thals Formation of unstable or non-functional Hgb types in alpha thalsThalassemia: 73 Thalassemia Severity ranges from lethal, to severe transfusion-dependency, to no clinical abnormalities; severity depends on the number and type of abnormal globin genes inherited. 1. Major severe anemia; no α (or β) chains are produced, so cannot make normal hemoglobin (s). Minor/trait mild anemia; slight decrease in normal hemoglobin types made.Beta Thal Major (Homozygous): 74 Heinz bodies Excess alpha chains Supravital stain Beta Thal Major (Homozygous) Both beta genes abnormal Marked decrease/absence of beta chains leads to alpha chain excess…no Hgb A is produced Rigid RBCs with Heinz bodies destroyed in bone marrow and blood (ineffective erythropoiesis)Beta Thal Major (Homozygous): 75 Stippled NRBC NRBC Target cell Wright’s stained blood smear HJB Beta Thal Major (Homozygous) Clinical findings Lab findings Severe anemia, target cells, nucleated red cells RBC inclusions No hemoglobin A; compensatory Hgb FBeta Thal Major (Homozygous): 76 Pap bodies NRBC Transfused RBC Target cell Hypercellular Bone Marrow (10x) Blood smear Howell-Jolly body Target cells Blood smear Transfused RBC Beta Thal Major (Homozygous) Treatment Transfusion Splenectomy Iron chelationBeta Thal Minor (Heterozygous): 77 Wright’s stained blood smear Stippled RBC Target cell Beta Thal Minor (Heterozygous) One abnormal beta gene Slight decreased rate of beta chain production Blood picture can look similar to iron deficiency Lab findings Mild anemia, target cells, no nRBCs, stippled RBCs No Heinz bodies Normal iron tests Compensates with Hgb A2 OvalocytesAlpha Thal Major/Homozygous: 78 Alpha Thal Major/Homozygous Deletion of all 4 alpha genes results in complete absence of alpha chain production No normal hemoglobin types made Known as Barts Hydrops Fetalis Die of hypoxia….Bart’s HgbAlpha Thal Intermedia = Hgb H Disease: 79 Target cells Wright’s stain blood smear Heinz bodies E xcess beta chains Supravital stain Alpha Thal Intermedia = Hgb H Disease Three alpha genes deleted Moderate decrease in alpha chains leads to beta chain excess…unstable Hgb H Moderate anemiaAlpha Thal Minor (Heterozygous): 80 Alpha Thal Minor (Heterozygous) One or two alpha genes deleted (group) Slight decrease in alpha chain production Mild or no anemia, few target cells Essentially normal electrophoresis; many undiagnosedBeta Thalassemias: 81 Beta ThalassemiasAlpha Thalassemias: 82 Alpha ThalassemiasDifferential Diagnosis of Microcytic Anemia: 83 + HGB Synthesis Defects Differential Diagnosis of Microcytic Anemia2. Macrocytic Normocytic Anemias: 84 2. Macrocytic Normocytic AnemiasMacrocytic Normocytic Anemias Characteristics ??????: 85 Macrocytic Normocytic Anemias Characteristics ?????? Wright’s stained blood smear: 86 A. MEGALOBLASTIC ANEMIA Vitamin B12 deficiency Folate deficiency Abnormal metabolism of folate and vit B12 B. Non megaloblastic anemia Liver disease Alcoholism Post splenoctomy Neonatal macrocytosis Stress erythropoiesisA. Megaloblastic Anemia : 87 A. Megaloblastic Anemia Macrocytosis due to a deficiency of vitamin B12 or folic acid that causes impaired nuclear maturation Vitamin B12 & folate are DNA coenzymes necessary for DNA synthesis and normal nuclear maturation Results in megaloblastic maturation…nucleus lags behind the cytoplasm and leads unbalanced growth called maturation asynchrony Both deficiencies cause enlarged fragile cells Many cells die in the marrow (ineffective) Show a similar blood picture and clinical findings Only vitamin B12 deficiency causes neurological symptoms…required for myelin synthesisMegaloblastic Anemia : 88 RBC maturation in microcytic anemias…IDA Normoblastic RBC maturation normocytic red cells Megaloblastic RBC maturation macrocytic red cells Megaloblastic AnemiaLab Findings of Megaloblastic Anemia: 89 Lab Findings of Megaloblastic Anemia Mild to severe anemia, Increased MCV & MCH, normal MCHC Low RBC, HGB, WBC and PLT counts (fragile cells) due to ineffective hematopoiesis. Low reticulocyte count Macrocytic ovalocytes and teardrops; Marked anisocytosis and poikilocytosis Schistocytes/microcytes - due to RBC breakage upon leaving the BM Erythroid hyperplasia - low M:E ratio (1:1) Iron stores increased.Slide 90: 90 Macrocytic Ovalocytes Blood NRBC Blood Howell-Jolly body Teardrop Schistocyte Stippled RBC & Cabot Ring Giant Platelet Pap bodies Hypersegmented Neutrophil >5 lobesVitamin B12 (Cobalamin) Deficiency: 91 Vitamin B12 (Cobalamin) DeficiencyVitamin B12 deficiency : 92 Vitamin B12 deficiency Occur as a result of one of the following conditions Nutritional Coballamin deficiency Strict vegetarianism Abnormal intragasteric events ( i.e. inadequate proteolysis of food Coballamin) atrophic gastritis. Loss or atrophy of gastric mucosa ( deficient IF) total or partial gasterectomy May develop B12 and iron deficiency with macro and micro red cells…a dual (dimorphic) RBC population pernicious anemiaCont…..: 93 Cont….. Abnormal events in the small bowel lumen Inadequate pancreatic protease Competing agents like fish tape worms (D.latum) Disorders of ileac mucosa Diminished or absent of IF – Coballamin receptor Drug effects Metabolic disorders ( coballamin is not used by cells)Folate (Folic acid) Deficiency: : 94 Folate (Folic acid) Deficiency: Deficient intake. Increased needs: pregnancy , infant , rapid cellular proliferation, and cirrhosis Malabsorption (congenital and drug-induced) Inherited DNA Synthesis Disorders: Deficient thiamine and factors (e.g. enzymes) responsible for folate metabolism. Toxins and Drugs: Two RBC populations Dimorphism Macrocytic RBCs Microcytic RBCs1. Pernicious Anemia : 95 1. Pernicious Anemia it is defined as anemia resulting from defective secretion of IF associated with autoimmune attack on the gastric mucosa leading to atrophy of the stomach or Abs that block IF action. Abs block the site of IF where vit B12 binds. The diagnosis is confirmed by low serum B12 level and typically abnormal results of schilling testSchilling test: 96 Schilling test Used to diagnose pernicious anemia and determine if IF is available. If absorbed a portion of oral dose of vit B 12 (not used by the body) ---- excreted in urine If not absorbed (malabsorption)…….. Not detected in urine but pass out in fecesSlide 97: 97 Stage I. To diagnose malabsorption give the patient a radio active cobalt labeled vit B12 orally and Non labeled vit B12 intramuscularly to saturate liver If IF is present in the stomach (no other disease) vit B12 is absorbed and labeled vit B12 detected in urine If absorption is impaired labeled vit B12 not detected in urine instead in stool Diagnose malabsorption if it is not appear in urine by proceeding stage II.Slide 98: 98 Stage II. Differentiate cause of malabsorption Oral dose labeled vit B12 + IF Appear in urine…… pernicious anemia (give IF) If not appear in urine it is other cause of malabsorptionSlide 99: 99 Performed to determine if the patient suffer from mal absorption of the IF – B12 complex secondary to small intestinal bacterial overgrowth. If this is the condition then tetracycline should normalize vit B12 absorption. Stage IIIB. Non-Megaloblastic Anemia: 100 Polychromatophilic RBCs Wright’s stain NRBC B. Non-Megaloblastic Anemia Macrocytosis that is NOT due to vitamin B12 or folate deficiency Accelerated erythropoiesis Regenerating marrow or marked reticulocyte response following recent blood lossNon-Megaloblastic Anemia: 101 Stomatocytes, Alcoholic Echinocytes Acanthocytes Target cells Non-Megaloblastic Anemia Liver disease and alcoholism Complex & multiple problems Degree of anemia varies, round macrocytes Target cells/acanthocytes - due to abnormal lipid metabolism. Echinocytes are also commonly found on the smear in liver disease.Differential Diagnosis of Macrocytic Anemia: 102 Blood smear Differential Diagnosis of Macrocytic Anemia Megaloblastic and non-Megaloblastic Perform B12 and folate levels Specific morphology3. Normocytic Normochromic Anemia: 103 3. Normocytic Normochromic Anemia3. Normocytic Normochromic Anemia: 104 3. Normocytic Normochromic Anemia It includes Aplastic anemia due to BM failure Blood loss anemia Hemolytic anemia Is a condition in which the size & Hgb content of RBCs is normal but the number of RBCs is decreased.A. Aplastic Anemia: 105 A. Aplastic Anemia Condition of blood pancytopenia caused by bone marrow failure…decreased production of all cell lines and replacement of marrow with fat. Due to damaged stem cells, damaged bone marrow environment or suppression No extramedullary hematopoiesisSlide 106: 106 Types of aplastic anemia Primary/idiopathic = 50% Secondary/acquired….chemicals, drugs, infections, radiation = 50% Congenital….Fanconi’s Aplasia plus dwarfism, skeletal abnormalities, mental retardation, abnormal skin pigmentation.Lab diagnosis of Aplastic Anemia: 107 Bone marrow, decreased # precursor cells 10X Normal RBCs No Platelets Blood Lab diagnosis of Aplastic Anemia Normochromic –Normocytic RBC (normal MCV & MCH) Low reticulocyte count & Hgb Pancytopenia No abnormal cells Hypoplasia Bone marrow Normal Serum iron, vitamin B12 and folate levelsB. Hemolytic anemia : 108 B. Hemolytic anemia Result from an increase in the rate of pre mature red cell destruction. Compensated hemolytic disease Uncompensated hemolytic disease It leads to Erythropoietic hyperplasia BM produces red cells 6 to 8X the normal rate Marked reticulocytosisHemolytic anemia: 109 Hemolytic anemia Two main mechanisms for RBC destruction in HA Intravascular hemolysis: in the circulation Extravascular hemolysis: in RE system (reticuloendothelial system)Extravascular hemolysis: 110 Extravascular hemolysis Aged RBC 120 day Abnormal RBC During destruction RBC releases Hgb Hgb Exstravascularly removed by Macrophage (RES) in BM, liver and spleen Iron reabsorbed Globin Amino acid Protein synthesis Protoporphyrin Unconjugated bilirubin liver (glucuronic acid) conjugated bilirubin gut reabsorbed & Excreted as urobilin & urobilinogenExtravascular hemolysis: 111 Extravascular hemolysis Lab features Increased RBC break down Serum bilirubin increase Stool urobilinogen increase Blood urobilinogen increase Urine urobilinogen increaseIntravascular hemolysis : 112 Intravascular hemolysis Red cells are destroyed in blood vessels and Hgb is released into the circulation: Free Hgb Saturates plasma haptoglobin Excess free Hgb is filtered by the glomerules (kidney) (if rate of hemolysis saturates renal reabsorption capacity) Free Hgb enters urine Fe is released in bladder tubule Renal tubule loaded with hemosiderinIntravascular hemolysis: 113 Intravascular hemolysis Lab features Hemoglobinemia and hemoglobinuria Hemosiderin uria Reduced/absent serum haptoglobin1. Hereditary hemolytic anemia: 114 1. Hereditary hemolytic anemia This is a congenital hemolytic anemia. some of which present at birth and other later in life, while still others may remain silent unless a physiological stress is super imposed Result of intrinsic red cell defects Membrane defect ( Hereditary Shperocytosis, Elliptocytosis and sickle cell anemia) Metabolic defect : G6PDH and PK defic Hgb chain defect (hemoglobinopatheis) : sickle cell anemiaA. Hemolytic Anemias due to Membrane Defects: 115 Spherocytes A. Hemolytic Anemias due to Membrane Defects Most common is Hereditary Spherocytosis (HS) Membrane defect is decreased spectrin and increased permeability of membrane to sodium ions Lab findings Anemia varies Few to many spherocytes on smear, high MCHC Increased OF testH Ovalocytosis/Elliptocytosis: 116 H Ovalocytosis Normocytic ovalocytes H Ovalocytosis/Elliptocytosis Membrane defect is polarization of cholesterol or hemoglobin at ends and increased sodium permeability Over 25% ovalocytes Most asymptomatic Mild anemia in 10-15%Hereditary Stomatocytosis: 117 H Stomatocytosis Hereditary Stomatocytosis Membrane defect is abnormal permeability to sodium and potassium Caused by edema 20-30% stomatocytes on blood smear Mild to severe hemolytic anemiaH Acanthocytosis: 118 H Acanthocytosis = Abetalipoproteinemia H Acanthocytosis Defect is increased membrane cholesterol due to abnormal plasma lipids Numerous acanthocytes on smear Mild anemia Also known as abetalipoproteinemiaOsmotic Fragility Test (OF): 119 Hypotonic Osmotic Fragility Test (OF) Most commonly used to diagnose Hereditary Spherocytosis Red cells are placed in hypotonic solutionsOsmotic Fragility Test (OF): 120 Osmotic Fragility Test (OF) Decreased Surface: Volume Ratio “Easy to Lyse” Increased Surface: Volume Ratio “Hard to Lyse”B. Defect red cell metabolism (Enzyme defect): 121 B. Defect red cell metabolism (Enzyme defect) G6PD deficiency G6PD is the only source of NADPH in red cell NADPH is reduced for the production of reduced Glutathione. Hgb and RBC membrane are usually protected from oxidant stress by reduced glutathione (GSH) In G6PD deficiency NADPH and GSH synthesis is impaired, rendering the red cells vulnerable to oxidant stress. Most individuals with G6PD are asymptomatic except during oxidant stress resulting from drugs or other causes.B. Hemolytic Anemias due to Enzyme Defects: 122 B. Hemolytic Anemias due to Enzyme Defects Inherited enzyme deficiencies that lead to premature RBC deathHemolytic Anemias due to Enzyme Defects: 123 PK Deficiency Echinocytes Hemolytic Anemias due to Enzyme Defects PK deficiency ↓ATP impairs cation pump Severe hemolytic anemia Echinocytes G-6-PD Deficiency Unable to protect Hgb due to decreased NADPH No clinical problems unless exposed to oxidants Exposure to oxidants induce Heinz body formation and RBC destruction Normal RBCs if no exposure to oxidant G-6-PD DeficiencyG-6-PD Deficiency: 124 G-6-PD deficiency after exposure to oxidant Heinz bodies - denatured Hgb Supravital stain G-6-PD deficiency Hemolytic episode Damaged RBCs Wright’s stain G-6-PD Deficiency Blood findings after oxidant exposure: Mod to severe anemia Schistocytes, spherocytes due to pitting out of Heinz bodies by spleen Enzyme assayC. Normocytic anemias due to hemoglobinopathies: 125 Target cells/Codocytes C. Normocytic anemias due to hemoglobinopathies Inherited hemoglobin defect with production of structurally abnormal globin chains; All have target cells Beta chain amino acid substitution = variant Hgb Hgb S = valine substituted for glutamic acid @ 6th of ß Hgb C = lysine substituted for glutamic acid @ 6th of ßHemoglobin S Disorders: 126 HGB S Disease (Hgb SS) Sickle cell Target cell Hemoglobin S Disorders Two sickle cell genes inherited (both beta chains are abnormal) Symptomatic after 6 months of age Lab findings Severe anemia Targets, sickle cells NRBCs, inclusions No Hgb A, >80% Hgb S, ↑ F A. Hemoglobin S disease/Sickle cell anemia/Hgb SSHemoglobin S Disorders: 127 Target cells only NO Sickle cells HGB S Trait (Hgb SA) Hemoglobin S Disorders One sickle cell gene inherited Lab findings Asymptomatic, targets only No anemia or sickle cells ~60% Hgb A, ~40% Hgb S Potential problems if hypoxic B. Hemoglobin S trait/Sickle cell trait/Hgb SAHemoglobin C Disorders: 128 C crystals HGB C Disease (Hgb CC) Target cell Hemoglobin C Disorders Lab findings Mild anemia Many target cells Intracellular C crystals No Hgb A, >90% Hgb C Decreased OF A. Hemoglobin C disease/Hgb CC Two C genes inherited ( both β chains are abnormal) C crystals polymerize differently and look like blocky Hgb packed rods in the red cells....intracellular.Hemoglobin C Disorders: 129 HGB C Trait (Hgb CA) Target cells only NO C crystals Hemoglobin C Disorders B. Hemoglobin C trait/Hgb CA One C gene inherited Lab findings Asymptomatic, no anemia Targets, no C crystals ~60% Hgb A, ~40% Hgb C Normal Hgb A2 and FHemoglobin SC Disease: 130 SC Crystals Target cells HGB SC Disease (Hgb S & Hgb C) Hemoglobin SC Disease Lab findings Intermediate in severity between Hgb SS & SA Several target cells Many SC crystals No Hgb A, ~50% Hgb S, ~50% Hgb C, ↑ F Hemoglobin SC disease/Hgb SC One sickle gene and one C gene inherited Double heterozygote‑ inherit sickle gene (S) from one parent and C gene from other parent; Both β chains are abnormal2. Acquired hemolytic anemia : 131 2. Acquired hemolytic anemia A variety of acquired conditions result in shortened survival of previously normal red cells. These include immune mediated destruction, red cell fragmentation disorders, acquired membrane defects, spleen effects Result of extrinsic causes Immune HA; warm HIHA, cold AIHA Drug associated Infection associatedWarm Autoimmune HA (WAIHA): 132 Spherocytes & polychromasia Blood Warm Autoimmune HA (WAIHA) Altered immune response causes production of an IgG warm autoantibody against ‘self’ RBC antigens Antibody/complement attaches to RBC antigen…partially phagocytosed (loss of membrane) spherocytes Cause: Primary (idiopathic) or secondary to diseaseWarm Autoimmune HA (WAIHA): 133 Ingestion of coated RBC RBC Electron Microscopy Blood Monocyte with ingested RBC RBC Warm Autoimmune HA (WAIHA) Lab findings Mod to severe anemia, spherocytes, high MCHC Erythrophagocytosis Looks similar to H spherocytosis but positive DAT Increased OF, bilirubin Erythroid hyperplasiaCold Autoimmune HA (CAIHA): 134 50x RBC Agglutination 100x Cold Autoimmune HA (CAIHA) Altered immune response causes production of an IgM cold autoantibody against ‘self’ RBC antigens Antibody/C3 attaches to RBC antigen agglutination (lysis by complement or macrophage) Primary (idiopathic) or secondary to diseaseCold Autoimmune HA (CAIHA): 135 Cold Autoimmune HA (CAIHA) Lab findings Agglutination of red cells in extremities....ears, toes, nose tissue damage gangre Severity varies with seasons….avoid the cold IgM antibodies cause RBC agglutination Reticulocytosis Positive Direct Antiglobulin Test (detects complement)Hemolytic Transfusion Reaction: 136 Hemolytic Transfusion Reaction Incompatible blood transfusion Recipient has antibodies to antigens on the donor red cells received Donor cells are destroyed ABO worst Intravascular hemolysis that is complement-induced lysis…immediate Can be life-threateningHemolytic Disease of the Newborn : 137 Hemolytic Disease of the Newborn Caused by maternal IgG antibodies directed against baby RBC antigens Antibodies cross placenta and destroy fetal red cells HDN due to Rh incompatibility Rh negative mother forms Rh antibody after exposure HDN due to Rh Sever anemia Many nucleated red cells HDN due to ABO incompatibility Mother’s ABO blood type is O; baby is type A or B HDN due to ABO Mild, no anemia SpherocytosisHemolytic Anemias due to Trauma: 138 Schistocytes Fibrin Strands RBC RBC fragmentation on fibrin strands Hemolytic Anemias due to Trauma Fragmentation syndromes…most common finding on smear are schistocytes; anemia varies Types of trauma Mechanical…prosthetic heart valves/cardiac abnormalities Microangiopathic (MAHA)…small vessels (DIC.........bleeding) March hemoglobinuria…forceful contact…. SchistocytesNormocytic/normochromic Hemolytic Anemias due to Trauma –: 139 Normocytic/normochromic Hemolytic Anemias due to Trauma – Fragmentation Syndromes A. When RBCs are exposed to excessive trauma within the cardiovascular system, they may undergo fragmentation and lysis. Schistocytes are the most common finding on the smear; RBC destruction tests are abnormal. Severe trauma causes intravascular hemolysis. B. Three types of trauma : 1. Mechanical trauma A. Prosthetic heart valves or cardiac abnormalities fragment red cells. B. Mod to severe anemia with schistocytes and polychromasia.Normocytic/normochromic Hemolytic Anemias due to Trauma –: 140 Normocytic/normochromic Hemolytic Anemias due to Trauma – 2. Microangiopathic hemolytic anemia (MAHA) – trauma occurs in small vessels Disseminated Intravascular Coagulation (DIC) is a widespread clotting disorder initiated by conditions such as OB obstetrical) complications or sepsis. In DIC, clotting factors and platelets form fibrin fibrin deposited in the microvessels fragment red cells. See anemia with schistocytes on smear, decreased platelets and depletion coagulation factors leads to severe bleeding; can be fatal. .Slide 141: 141 2. Microangiopathic hemolytic anemia (MAHA) cont’d…….. Hemolytic uremic syndrome (HUS) - most often occurs in children following GI infection (E. coli); noted for renal failure fibrin damages kidney; hemolytic anemia with echinocytes and schistocytes, decreased platelets; often requires dialysis; can be fatalNormocytic/normochromic Hemolytic Anemias due to Trauma –: 142 Normocytic/normochromic Hemolytic Anemias due to Trauma – 3. March Hemoglobinuria Transient, occurs after forceful contact of body with hard surfaces....joggers, soldiers after long march, bongo drum players. Hemoglobinuria; schistocytes may be present on smear.Hemolytic Anemias due to Infectious Agents, and Thermal Burns: 143 Schistocytes & Spherocytes Hemolytic Anemias due to Infectious Agents, and Thermal Burns Anemia varies, with severe hemolysis Schistocytes and spherocytes on blood smear Parasitize RBC, elaborate lytic toxins or cause direct damage to red cell membrane Malaria fever Closteridal infections..release toxinsNormocytic/normochromic Hemolytic Anemia due to Infectious Agents : 144 Normocytic/normochromic Hemolytic Anemia due to Infectious Agents A. Malarial infection 1. Damage to membrane occurs when parasite is pitted out of red cell by splenic macrophages or the entire RBC is removed; chills and fever as red cells rupture. 2. P. falciparum causes severe hemolysis called Blackwater fever.Normocytic/normochromic Hemolytic Anemia due to Infectious Agents: 145 Normocytic/normochromic Hemolytic Anemia due to Infectious Agents Clostridial infections - Clostridia elaborate toxins which damage RBC membrane causing severe intravascular hemolysis. Both malaria and clostridial infections are characterized by schistocytes and spherocytes on the blood smear; other infectious organisms can cause hemolysis, e.g. Toxoplasma, Bartonella, Babesia, Ehrlichia.END OF ANEMIA : 146 END OF ANEMIA You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.