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MLAB 1415- Hematology Keri Brophy-Martinez
Iron Metabolism and Hypochromic Anemias
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Iron Metabolism Primary function Oxygen transport and storage
Distribution Types of iron-containing compounds Functional, assisting in enzymatic and metabolic functions Transportation or storage Location RBCs- majority here Macrophages of spleen& liver- where destruction of RBC occurs, liberating iron Hepatocytes and enterocytes- storage of iron
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Iron Metabolism Iron absorption and storage is influenced by:
The amount and type of available iron in the diet Is it a nutritional deficiency Incomplete absorption due to GI tract problems Current iron stores Increased demand (pregnancy, the growth years) Excessive loss due to acute or chronic hemorrhage menstrual period for women of childbearing years, GI bleeding for men
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Forms of Iron Nonheme Heme Ionic or ferric
Found in vegetables and whole grains Heme Found in red meats Easily absorbed
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Iron Metabolism Transport Transferrin
Transports iron to bone marrow to be used in hgb synthesis Synthesized in the liver Storage Primarily in the liver Ferritin Soluble iron, quick release for heme synthesis Hemosiderin Partially degraded iron, slow release
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Iron Balance Loss of iron Regulation of iron
Secretions of urine, bile , sweat and exfoliation of intestinal epithelial cells of GI tract Approx. 1 mg/ day Regulation of iron Delicate balance between loss and absorption
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Laboratory Assessment of Iron
Serum iron Total iron binding capacity (TIBC) Percent saturation Serum ferritin
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Clinical Syndromes of Iron Metabolism
Iron Deficiency Anemia (IDA) AKA Sideropenic anemia This is the most common form of anemia. IDA occurs when the iron stores in the body are inadequate to preserve homeostasis.
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Causes of IDA Dietary Blood Loss Hemodialysis Malabsorption
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3 Stages of IDA Stage 1 Decrease in storage iron (ferritin decrease)
No anemia RBC morphology normal RDW can be elevated Stage 2 Decrease in iron for erythropoiesis No anemia or hypochromia RBC slightly microcytic Stage 3 Decrease in Blood Hgb Decrease in peripheral tissue oxygen delivery All lab tests abnormal Microcytic, hypochromic anemia
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Clinical Features of IDA
SOB Lethargy Pallor Gastritis Pica Koilonychia
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IDA: Lab features Decreased RBC, Hgb, Hct, MCV, MCH, MCHC
Normal to decreased Retic Peripheral blood smear microcytic-hypochromic Targets, elliptocytes, teardrops If IDA is caused by bleeding, leukocytosis and thrombocytosis are possible.
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IDA: Lab Findings Chemistry Bone marrow Decrease in stainable iron
Mild-moderate erythroid hyperplasia M:E ratio decreased Chemistry Decrease in serum iron and ferritin Increased TIBC
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Anemia of Chronic Inflammation
Anemia that occurs in patients with chronic infections, chronic inflammatory disorders, trauma, organ failure or neoplasms Occurs due to biochemical changes during inflammation Hepcidin- acute phase reactant Hallmark is normal- increased ferritin but low serum iron
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Anemia of Chronic Inflammation: Lab Features
Typical lab findings Decreased RBC, Hgb, Hct, MCV, MCH, serum iron, transferrin Normal to Increased ferritin Normal MCHC Normal to Decreased Retic, TIBC Peripheral blood smear normocytic-normochromic Targets, elliptocytes, teardrops Bone marrow M:E ratio increased
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Anemia’s Associated with Abnormal Heme Synthesis
Sideroblastic Anemia Lead Poisoning Porphyrias
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Sideroblastic Anemia (SA)
First step in heme synthesis is affected Characterized by: Increase in total body iron Presence of ringed sideroblasts in bone marrow Hypochromic anemia
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Classification Sideroblastic anemia Hereditary Acquired 2 Forms
Idiopathic Secondary type Certain therapeutic drugs Chronic transfusions (for aplastic anemia, leukemia, thalassemia) Alcoholism and food fads Use of iron utensils or increased iron in water .
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Sideroblastic anemia Mechanism
Adequate iron but it can not be incorporated into hgb synthesis. Iron enters mitochrondria of metarubricyte, but accumulates leading to formation of ringed sideroblasts Eventually, mitochrondria rupture
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Lead poisoning Lead interferes with iron storage in the mitochondria
Lead damages the activity of enzymes used for heme synthesis Basophilic stippling pronounced
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Lead Poisoning
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Lab features of SA Peripheral blood Pappenheimer bodies
Hypochromic, normochromic RBCs Normal to increased platelets Chemistry Increased serum iron, ferritin Decreased TIBC
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Hemochromatosis Condition caused by increased iron absorption which deposits in vital organs such as the liver, spleen and pancreas which then becomes fibrotic Hyperpigmentation of skin Therapy consists of iron removal by therapeutic phlebotomy or chelation
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Lab Features of Hemochromatosis
Increased Iron Ferritin Decreased TIBC Transferrin
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Porphyrias Excessive production of porphyrins in the bone marrow (or liver) Rare disease caused by accumulation of porphyrins in developing RBC’s Defect in one or more of the enzymes in heme synthesis pathway Characterized by dermal photosensitivity and rash caused by the sun. The original werewolf was probably a person with erythropoietic porphyria.
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References Harmening, D. M. (2009). Clinical Hematology and Fundamentals of Hemostasis. Philadelphia: F.A Davis. McKenzie, S. B., & Williams, J. L. (2010). Clinical Laboratory Hematology . Upper Saddle River: Pearson Education, Inc.
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