* Symptoms: -Shortness of breath (particularly on exercise) -Weakness -Lethargy -Palpitation -Head aches * In Older Subject: -Cardiac failure -Angina pectoris -Confusion -Intermittent claudication SYMPTOMS * General: -Pallor of mucous membrane (less than 9 d/dl) -Tachycardia -Cardiomegali -Syst flow murmur (especially at the apex) -Retinal hemorhages (unusual) -In the elderly: congestive hearth failure * Specific: -Koilonychia (spoon nails) iron def. -Jaundice hemolytic or megaloblastic anemia -Leg ulcers sickel cell A -Bone deformities thalasssemia major -Neugopathy vit. B12 def. Classification based on red cell indices Normocytic, normochromic Macrocytic Microcytic, hypochromic Microcytic, hypochromic MCV < 80 fl MCH < 27 pg Clinically: - Iron def. - Thalassemia - Anemia of chronic disease (some cases) - Lead poisoning - Sideoblastic anemia (some cases)
Normocytic, Normochromic MCV : 80 - 95 fl MCH : > 26 pg Clinically: - Hemolitic Anemia - Anemia of chronic disease (some cases) - After acut blood loss - Renal disease - Mixed deficiencies - Bone marrow failure
Macrocytic MCV : > 95 fl Hypersegmented Neutrophil Five Lobes Clinically: - Megaloblastic : vit B12 or folate def. - Non megaloblastic: ^ Alcohol ^ Liver disease ^ Myelodysplasia ^ Aplastic anemia Anemia with the varation in size (anysocytosis) and Shape (poikilocytosis) ( 1 ) Red cell abnormalities Causes -Macrocyte - liver disease - alcoholism -Target cell - iron def. , liver dis - hemoglobinopathy - post splenectomy -Stomotocyte - liver disease, alcoholism -Pencil cell - iron def. -Ecchinocyte - liver disease - post splenectomy
Anemia with the varation in size (anysocytosis) and Shape (poikilocytosis) ( 2 ) Red cell abnormalities Causes -Microspherocyte - hereditary spherocytosis - AIHA, septicemia -Fragments - DIC, microangiopati HUS,TTP Burs,cardiac valve -Elliptocyte - hereditary elliptocytosis -Tear drop - Myelofibrosis, extramedullary hemopoiesis -Basket cell - Oxydant damage e.g. G6PD -Sickle cell - Iron deficiency -Microcyte - Hemoglobinopathy
Reticulocyte count Normal : 0.5 - 1.5 % reticulocyte : Anemia Hemolytic anemia After an acut major hemorrhagic Within 2 3 days Reaches a maximum in 6 10 days Remains raised until th Hb returns to normal level Factor impairing the normal reticulocyte response to anemia Marrow disease Hipoplasia Infiltration by carcinoma Lymphoma, myeloma, acut leukemia Deficiency of iron, Vit. B12, Folic acid Lack of erythropoietin eg. Renal disease Reduced tissue O2 consumption e.g mixooedema, protein def. In effective erythropoiesis, thalassemia nyelodisplasia Chronic inflammatory or malignant disease Leukocyte and Platelet Count Measurement of these help to distingguish pure anemia from pancytopenia (marrow hypoplasia, hypersplenisme) Biopsi 1. Site : posterior iliac crest 2. Stains : haematoxylin and eosin, reticulin (silver stain) 3. Indication: - Suspicion of polycythemia vera - Nyelofibrisis and other myeloproliferative disorders - Aplastic anemia - Malignant lymphoma - Secondary carcinoma - Cases of splenomegali or pyrexia of undetermined - Any case where aspiration give cause a dry tap 4. Special test : Immunophenotyping
Assesment of erythropoiesis Normal erythropoiesis Decrease erythropoiesis (eg. Aplastic anemia) Increase erythropoiesis (eg. Hemolytic anemia) In effective erythropoiesis (Megaloblastic anemia)
T h e r a p y Underlying disease Hematinic : - Ferrum - Vit. B 12 - Folic Acid