Blood Disease Definitions Flashcards
Basic Definitions of Blood Diseases with some signs and symptoms.
Anemia Due to Blood Loss
Acute: GI bleed; Injury; Surgery Chronic: Bladder tumors Cancer or polyps in GI tract Heavy menstrual bleeding Kidney tumors Ulcers in the stomach or small intestine
Microcytic Anemia
Microcytic anemias result from deficient or defective heme or globin synthesis. Microcytic anemias include iron deficiency anemias, iron-transport deficiency anemias, iron-utilization anemias (including some sideroblastic anemias and lead poisoning), and thalassemias (which also cause hemolysis).
Normochromic-normocytic Anemia
Normocytic anemias are characterized by a normal RBC distribution width (RDW) and normochromic indices. The two most common causes are hypoproliferation due to a deficiency of or inadequate response to erythropoietin (EPO) and anemia of chronic disease. (thyroid disease, kidney disease)
Macrocytic Anemia
Macrocytic anemias can be caused by impaired DNA synthesis leading to megaloblastosis, as occurs with deficiencies of vitamin B12 or folate (see Megaloblastic Macrocytic Anemias). Other causes include chronic alcohol intake (independent of vitamin deficiency), liver disease, myelodysplastic syndrome (MDS), and hemolysis. Some patients with hypothyroidism have macrocytic RBC indices, including some without anemia.
Anemia S/S
Symptoms include: ● Tiredness. ● Lightheadedness. ● coexisting disease, e.g. angina. Signs include: ● Mucous membrane pallor. ● murmurs. ● Ankle oedema. ●Tachypnoea. ● Raised JVP. ● Postural hypotension. ●tachycardia
Leucopenia
low WBC count
Leucocytosis
high WBC count
Neutrophilia Causes
High Neutrophil Count: Infection. ● Trauma. ● Myocardial infarction (MI). ●Inflammation ● Malignancy. ● Myeloproliferative disorders.
Lymphocytosis
High Lymph count; Most commonly seen in viral infections
Eosinophilia
High Eosinophil Count; Allergy ( asthma, drug reactions etc.), Parasitic Infections; Inflammatory Disease; Malignancy.
Lymphadenopathy
Enlarged Lymph Nodes
Splenomegaly
Enlarged Spleen
Thrombocytopenia
Low Platelet Count
Thrombocytosis
High Platelet Count
Megaloblastic anaemia
This results from deficiency of vitamin B12
or folic acid, both of which are required for DNA synthesis.
Pernicious anaemia
This is an autoimmune disorder characterised by atrophy of the gastric mucosa. Loss of the parietal cells causes intrinsic factor deficiency, leading to vitamin B12
malabsorption.
Haemolytic anaemia
When destruction exceeds production, haemolytic anaemia results
Sickle-cell anaemia
When HbS is deoxygenated, the Hb molecules polymerise and the red cell membrane becomes distorted, producing characteristic sickle-shaped cells
thalassaemias
thalassaemias are a group of inherited disorders of Hb production in which there is impaired synthesis of alpha or beta globin chains. The resultant imbalance in the ratio of alpha to beta chains leads to precipitation of the excess chains, causing membrane damage and reduced red cell survival.
Leukemias
Leukaemias are malignant disorders of haematopoietic stem cells, associated with increased numbers of white cells in the bone marrow and/or peripheral blood
Types of Leukemias
Acute lymphoblastic leukaemia (ALL).(most common in children) ●
(AML). ● Chronic lymphocytic leukaemia (CLL). ● leukaemia (CML)
Acute Leukemias
Acute leukaemias occur at all ages, but ALL has a peak incidence in children aged 1–5 yrs. AML occurs mainly over the age of 50
Most Common Type of Leukemia
Chronic lymphocytic leukaemia (CLL) is the most common variety of leukaemia, typically presenting between the ages of 65 and 70 yrs.
Cytopenia
Cytopenia is a reduction in the number of mature blood cells.
Hodgkin lymphomas
Hodgkin lymphoma is a localized or disseminated malignant proliferation of cells of the lymphoreticular system, primarily involving lymph node tissue, spleen, liver, and bone marrow. (B-Cell)
Non-Hodgkin lymphomas (NHL)
Non-Hodgkin lymphomas (NHL) are a heterogeneous group of disorders involving malignant monoclonal proliferation of lymphoid cells in lymphoreticular sites, including lymph nodes, bone marrow, the spleen, the liver, and the GI tract. (B-Cell and T-Cell origin)
Multiple myeloma
This is a malignant proliferation of plasma cells and has a peak incidence between the ages of 60 and 70 yrs
aplastic anaemia
This is a rare disorder in Europe and North America. It is characterised by failure of the pluripotent stem cells, resulting in hypoplasia of the bone marrow with pancytopenia
erythropoiesis
production of RBCs