This document lists 24 named points related to blood vessels and the heart. Some key points include onion skin lesions seen in hyperplastic arteriosclerosis, Monckeberg medial sclerosis where calcific deposits are seen in muscular arteries in people over 50, contraction bands seen when perfusion is re-established in the heart, and mitral valve prolapse where the key change is myxomatous degeneration and interchordal ballooning of the mitral valve leaflets.
This document discusses leukocytosis, an increased number of white blood cells in the blood. It describes the different types of white blood cells and their normal functions. Leukocytosis can be caused by infections, inflammatory disorders, cancers, and medications. The main types of leukocytosis are neutrophilia, lymphocytosis, monocytosis, eosinophilia, and basophilia. Reactive leukocytosis is usually a response to infection or inflammation, while very high or persistent leukocytosis may indicate leukemia or other diseases.
The document discusses white blood cells (WBCs) and hematopoiesis, the process of blood cell production. It notes that before birth, hematopoiesis occurs in the liver, while after birth it occurs solely in the bone marrow. The bone marrow contains hematopoietic stem cells that differentiate into the various blood cell types, including erythrocytes, granulocytes, and platelets. WBCs are divided into granulocytes and agranulocytes, with the main types being neutrophils, basophils, eosinophils, lymphocytes, and monocytes. The document provides details on the function and characteristics of each WBC type.
The document contains four tables that list various causes of splenomegaly (enlarged spleen) and hyposplenism (underactive spleen), indications for splenectomy (surgical spleen removal), and vaccination recommendations for patients with hyposplenism. Table 10.1 lists hematological, portal hypertension, storage, systemic, and infectious diseases as potential causes of splenomegaly. Table 10.2 describes blood film features seen in different causes of hyposplenism. Table 10.3 provides indications for splenectomy such as splenic rupture, various hematological disorders, and tropical splenomegaly. Table 10.4 gives vaccination recommendations for pneumococcal, meningococ
Leukocyte is another name for white blood cell (WBC). These are the cells in your blood that help your body fight infections and some diseases.
When the number of white cells in your blood is higher than normal, it’s called leukocytosis. This usually happens because you’re sick, but sometimes it’s just a sign that your body is stressed.is a condition that affects all types of white blood cells. Other illnesses, such as neutrophilia, lymphocytosis, and granulocytosis, target specific types of white blood cells. Normal white blood cell counts are 4,300-10,800 white blood cells per microliter. Leukocyte or white blood cell levels are considered elevated when they are between 15,000-20,000 per microliter. The increased number of leukocytes can occur abnormally as a result of an infection.An abnormally large number of leukocytes, as observed in acute infections, inflammation, hemorrhage, and other conditions. A white blood cell count of 10,000/mm3 (or more) usually indicates leukocytosis Most examples of leukocytosis represent a disproportionate increase in the number of cells in the neutrophilic series, and the term is frequently used synonymously with the designation neutrophilia. Leukocytosis of 15,000-25,000/mm3 is frequently observed in various pathologic conditions, and values as high as 40,000 are not unusual; occasionally, as in some examples of leukemoid reactions, white blood cell counts may range up to 100,000/mm3.Leukocytosis is usually a response to an infection or inflammation, so it’s not a cause for alarm. However, it can be caused by serious diseases such as leukemia and other cancers, so it’s important that your doctor diagnose the cause of an increased WBC when it’s found. Leukocytosis associated with pregnancy or in response to exercise is normal and nothing to worry about.
Blood diseases cover a wide spectrum of illnesses, ranging from the anaemias, leukaemias and congenital coagulation disorders.
Haematological change may occur as a consequence of disease affecting any system and measurement of haematological parameters is an important part of routine clinical assessment.
This document discusses the structure and functions of different types of leukocytes (white blood cells) found in the blood. It describes the characteristics and roles of granulocytes like neutrophils, eosinophils, and basophils. It also summarizes monocytes, lymphocytes, platelets, and plasma cells - discussing their origins, structures, and functions in the immune system and blood clotting process.
This document lists 24 named points related to blood vessels and the heart. Some key points include onion skin lesions seen in hyperplastic arteriosclerosis, Monckeberg medial sclerosis where calcific deposits are seen in muscular arteries in people over 50, contraction bands seen when perfusion is re-established in the heart, and mitral valve prolapse where the key change is myxomatous degeneration and interchordal ballooning of the mitral valve leaflets.
This document discusses leukocytosis, an increased number of white blood cells in the blood. It describes the different types of white blood cells and their normal functions. Leukocytosis can be caused by infections, inflammatory disorders, cancers, and medications. The main types of leukocytosis are neutrophilia, lymphocytosis, monocytosis, eosinophilia, and basophilia. Reactive leukocytosis is usually a response to infection or inflammation, while very high or persistent leukocytosis may indicate leukemia or other diseases.
The document discusses white blood cells (WBCs) and hematopoiesis, the process of blood cell production. It notes that before birth, hematopoiesis occurs in the liver, while after birth it occurs solely in the bone marrow. The bone marrow contains hematopoietic stem cells that differentiate into the various blood cell types, including erythrocytes, granulocytes, and platelets. WBCs are divided into granulocytes and agranulocytes, with the main types being neutrophils, basophils, eosinophils, lymphocytes, and monocytes. The document provides details on the function and characteristics of each WBC type.
The document contains four tables that list various causes of splenomegaly (enlarged spleen) and hyposplenism (underactive spleen), indications for splenectomy (surgical spleen removal), and vaccination recommendations for patients with hyposplenism. Table 10.1 lists hematological, portal hypertension, storage, systemic, and infectious diseases as potential causes of splenomegaly. Table 10.2 describes blood film features seen in different causes of hyposplenism. Table 10.3 provides indications for splenectomy such as splenic rupture, various hematological disorders, and tropical splenomegaly. Table 10.4 gives vaccination recommendations for pneumococcal, meningococ
Leukocyte is another name for white blood cell (WBC). These are the cells in your blood that help your body fight infections and some diseases.
When the number of white cells in your blood is higher than normal, it’s called leukocytosis. This usually happens because you’re sick, but sometimes it’s just a sign that your body is stressed.is a condition that affects all types of white blood cells. Other illnesses, such as neutrophilia, lymphocytosis, and granulocytosis, target specific types of white blood cells. Normal white blood cell counts are 4,300-10,800 white blood cells per microliter. Leukocyte or white blood cell levels are considered elevated when they are between 15,000-20,000 per microliter. The increased number of leukocytes can occur abnormally as a result of an infection.An abnormally large number of leukocytes, as observed in acute infections, inflammation, hemorrhage, and other conditions. A white blood cell count of 10,000/mm3 (or more) usually indicates leukocytosis Most examples of leukocytosis represent a disproportionate increase in the number of cells in the neutrophilic series, and the term is frequently used synonymously with the designation neutrophilia. Leukocytosis of 15,000-25,000/mm3 is frequently observed in various pathologic conditions, and values as high as 40,000 are not unusual; occasionally, as in some examples of leukemoid reactions, white blood cell counts may range up to 100,000/mm3.Leukocytosis is usually a response to an infection or inflammation, so it’s not a cause for alarm. However, it can be caused by serious diseases such as leukemia and other cancers, so it’s important that your doctor diagnose the cause of an increased WBC when it’s found. Leukocytosis associated with pregnancy or in response to exercise is normal and nothing to worry about.
Blood diseases cover a wide spectrum of illnesses, ranging from the anaemias, leukaemias and congenital coagulation disorders.
Haematological change may occur as a consequence of disease affecting any system and measurement of haematological parameters is an important part of routine clinical assessment.
This document discusses the structure and functions of different types of leukocytes (white blood cells) found in the blood. It describes the characteristics and roles of granulocytes like neutrophils, eosinophils, and basophils. It also summarizes monocytes, lymphocytes, platelets, and plasma cells - discussing their origins, structures, and functions in the immune system and blood clotting process.
White blood cells, also known as leukocytes, come in various types classified by their granule presence and cytoplasm staining. The five main types are granulocytes (neutrophils, eosinophils, basophils) and agranulocytes (lymphocytes, monocytes). Leukocytes are formed in bone marrow and live around 13-20 days, playing important roles in immunity and fighting infection and disease. Leukocyte disorders include increased or decreased cell counts caused by various infections, cancers, drugs, or medical conditions.
A myeloprolifrative stem cell disorder resulting in
Proliferation of all haematopoietic lineages but
manifestation Predominantly in the granulocytic series.
The disease occurs chiefly between 30 and 80 years, with
A peak incidence at the 55 years.
*accounts for 20% of all leukaemis.
*found in all races.
*the aetiology is unknown.
POWERPOINT PRESENTATION ON WHITE BLOOD CELLSVidya P Pillai
The document discusses the different types of white blood cells (leukocytes). There are two main types: granulocytes which contain granules in their cytoplasm, and agranulocytes which do not contain granules. The granulocytes - neutrophils, eosinophils, and basophils - make up the majority of white blood cells and function to phagocytose foreign materials. The agranulocytes, lymphocytes and monocytes, have clear cytoplasm and play important roles in fighting viruses, tumors, and bacteria.
The document discusses blood cell production and erythropoiesis, the formation of red blood cells. It notes that red blood cells are produced in the red bone marrow at a baseline rate of about 20% of total capacity to maintain health. Approximately 2.4 million red blood cells must be replaced every second to make up for the 120-day lifespan of red blood cells. Prolonged oxygen depletion in the blood, like severe blood loss, anemia, clogged blood vessels, or low atmospheric oxygen, stimulates the kidneys to secrete erythropoietin, which targets the bone marrow and increases red blood cell production.
Acute myelogenous leukemia (AML) is a cancer of the blood and bone marrow characterized by the rapid growth of abnormal white blood cells that build up in the bone marrow and interfere with normal blood cell production. AML results from genetic mutations that cause immature myeloid cells to proliferate uncontrollably. Diagnosis involves blood tests, bone marrow aspiration and biopsy, and cytogenetic analysis. Treatment consists of induction chemotherapy to achieve remission followed by consolidation chemotherapy to destroy any remaining leukemia.
The document discusses pericardial effusion, which is an abnormal accumulation of fluid in the pericardial sac surrounding the heart. It can be caused by various conditions that obstruct fluid drainage or damage the pericardium, such as infection, malignancy, autoimmune diseases, or drugs. The document lists various infectious etiologies of pericardial effusion including bacteria, viruses, fungi, and protozoa. It also discusses non-infectious causes like cancer and connective tissue diseases. Routine testing of pericardial fluid includes cell count, glucose, protein and LDH levels to help determine the cause.
Leukopoiesis is the formation and maturation of white blood cells. It occurs primarily in the bone marrow through a series of mitosis and differentiation of stem cells into various white blood cell types. The major white blood cell types produced are granulocytes like neutrophils, eosinophils and basophils through granulopoiesis; monocytes through monocytopoiesis; and lymphocytes through lymphopoiesis. Leukopoiesis is regulated by growth factors and cytokines that influence the proliferation and specialization of stem cells in the bone marrow microenvironment.
Leukocytosis is an increase in the number of white blood cells. It occurs as part of the body's inflammatory response. The level of white blood cells is regulated by the rate of production and release from bone marrow and other storage sites, as well as the rate that cells exit the bloodstream into tissues. Leukocytosis can be caused by cytokines and growth factors that stimulate the differentiation and proliferation of specific white blood cell types, such as interleukin-5 for eosinophils and G-CSF for neutrophils. In severe inflammatory conditions, leukocytes may display abnormal morphologies including toxic granules, Dohle bodies, and cytoplasmic vacuoles.
This document provides an introduction to the field of pathology and laboratory medicine. It discusses the various careers available, including pathologists, medical laboratory scientists, and phlebotomy technicians. It also outlines the different departments in a medical laboratory, such as clinical chemistry, microbiology, and hematology. Key components of a complete blood count and different types of blood cells are defined. Abnormal blood cells and diseases like sickle cell anemia and leukemia are mentioned. Identification of microorganisms through gram staining is briefly introduced.
The document discusses leucocytes (white blood cells). It describes the classification of WBCs into granulocytes and agranulocytes. Granulocytes include neutrophils, eosinophils, and basophils which are involved in phagocytosis and immune responses. Agranulocytes include lymphocytes and monocytes. Lymphocytes provide humoral and cellular immunity while monocytes circulate in blood and differentiate into tissue macrophages. The reticuloendothelial system comprised of macrophages is also described which acts as a generalized phagocytic system in the body.
The document discusses hematopoiesis, the process of blood cell production. It describes how hematopoietic stem cells in the bone marrow differentiate into the various blood cell lineages through the action of growth factors. This includes erythropoiesis, granulopoiesis, megakaryopoiesis, and lymphopoiesis. It also covers reactive conditions that can cause changes in white blood cell counts, such as infections and inflammatory states.
The document provides information on differential leukocyte counting (DLC). It defines DLC as the relative proportion of different leukocytes expressed as a percentage. The main types of white blood cells (WBCs) described are granulocytes (neutrophils, eosinophils, basophils) and agranulocytes/mononuclear cells (lymphocytes, monocytes). Pathologic variations in DLC counts include neutrophilia, neutropenia, lymphocytosis, lymphopenia, monocytosis, eosinophilia, eosinopenia, and basophilia. Causes of each variation are outlined. Automated methods for differential counting are also discussed and compared to manual microscopic methods
This document discusses the analysis of blood components. It covers:
- The functions of blood including oxygen transport, waste removal, temperature regulation, and more.
- Types of blood testing done in hematology, immunology, blood banking, and chemistry sections.
- Components of a complete blood count including red blood cell count, white blood cell count, hemoglobin, hematocrit, and differential white blood cell count.
- The different blood cell types - red blood cells, white blood cells (granulocytes and agranulocytes), platelets, and their roles in the body.
- Procedures for examining blood smears and determining cell counts are also outlined.
This document discusses white blood cells (WBCs), also known as leukocytes. It begins with definitions of WBC and explains they help the body's defense mechanisms. It describes WBC composition and the normal total count range. It then classifies WBCs into granulocytes and agranulocytes and lists the types in each group. The document outlines the functions of neutrophils, monocytes, lymphocytes, eosinophils and basophils. It concludes with the method and calculation for determining total WBC count using a hemocytometer.
White blood cells, or leukocytes, are cells of the immune system that defend the body against infectious disease and foreign materials. There are five main types of leukocytes - granulocytes (neutrophils, basophils, eosinophils) and agranulocytes (lymphocytes, monocytes). Granulocytes contain granules that help them digest pathogens, while agranulocytes do not contain granules. Leukocytes are produced in the bone marrow and circulate throughout the body in blood and lymph fluid. An abnormal increase or decrease in the number of leukocytes can indicate certain diseases.
White blood cells have varying lifespans depending on their type. Granulocytes last 4-8 hours in circulation and a few more days in tissues. Monocytes last 10-20 hours in blood and months in tissues as macrophages. Lymphocytes circulate for weeks or months between lymphoid tissue, blood, tissues, and lymph before returning to blood. Disorders that can affect white blood cell counts include leucopenia from radiation or chemicals, and leukemias like lymphocytic or myelogenous leukemia, which can lead to infections, anemia, bleeding, and lack of energy.
This document discusses white blood cell disorders, focusing on quantitative disorders of the white blood cells. It describes leukocytosis, which is an increased number of white blood cells, and leukopenia, which is a decreased number. The main types of leukocytosis and leukopenia discussed are neutrophilic leukocytosis, lymphocytosis, and eosinophilia. The causes, pathophysiology, and clinical features of each of these conditions are explained in detail.
presented by HAFIZ M WASEEM
university of education LAHORE Pakistan
i am from mailsi vehari and studied in lahore
bsc in science college multan
msc from lahore
The document summarizes the major functions and components of blood. It discusses how blood transports oxygen, nutrients, hormones and removes waste products while regulating pH and temperature. Blood also protects the body through clotting and the immune response. The components of blood include red blood cells, white blood cells, platelets and plasma. Abnormalities can cause issues like anemia or clotting disorders.
acute leukemia
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This document provides information about acute lymphoblastic leukemia (ALL). It discusses that ALL is a cancer of the lymphoid cells that is most common in children. The document covers the classification, immunologic subtypes, cytogenetic abnormalities, clinical features, diagnostic measures, and hematological and histological findings of ALL. It describes that ALL is diagnosed based on complete blood count, peripheral smear, bone marrow biopsy and cytogenetic/flow cytometry analysis. The key diagnostic findings include anemia, leukocytosis, thrombocytopenia and lymphoblasts in the bone marrow.
White blood cells, also known as leukocytes, come in various types classified by their granule presence and cytoplasm staining. The five main types are granulocytes (neutrophils, eosinophils, basophils) and agranulocytes (lymphocytes, monocytes). Leukocytes are formed in bone marrow and live around 13-20 days, playing important roles in immunity and fighting infection and disease. Leukocyte disorders include increased or decreased cell counts caused by various infections, cancers, drugs, or medical conditions.
A myeloprolifrative stem cell disorder resulting in
Proliferation of all haematopoietic lineages but
manifestation Predominantly in the granulocytic series.
The disease occurs chiefly between 30 and 80 years, with
A peak incidence at the 55 years.
*accounts for 20% of all leukaemis.
*found in all races.
*the aetiology is unknown.
POWERPOINT PRESENTATION ON WHITE BLOOD CELLSVidya P Pillai
The document discusses the different types of white blood cells (leukocytes). There are two main types: granulocytes which contain granules in their cytoplasm, and agranulocytes which do not contain granules. The granulocytes - neutrophils, eosinophils, and basophils - make up the majority of white blood cells and function to phagocytose foreign materials. The agranulocytes, lymphocytes and monocytes, have clear cytoplasm and play important roles in fighting viruses, tumors, and bacteria.
The document discusses blood cell production and erythropoiesis, the formation of red blood cells. It notes that red blood cells are produced in the red bone marrow at a baseline rate of about 20% of total capacity to maintain health. Approximately 2.4 million red blood cells must be replaced every second to make up for the 120-day lifespan of red blood cells. Prolonged oxygen depletion in the blood, like severe blood loss, anemia, clogged blood vessels, or low atmospheric oxygen, stimulates the kidneys to secrete erythropoietin, which targets the bone marrow and increases red blood cell production.
Acute myelogenous leukemia (AML) is a cancer of the blood and bone marrow characterized by the rapid growth of abnormal white blood cells that build up in the bone marrow and interfere with normal blood cell production. AML results from genetic mutations that cause immature myeloid cells to proliferate uncontrollably. Diagnosis involves blood tests, bone marrow aspiration and biopsy, and cytogenetic analysis. Treatment consists of induction chemotherapy to achieve remission followed by consolidation chemotherapy to destroy any remaining leukemia.
The document discusses pericardial effusion, which is an abnormal accumulation of fluid in the pericardial sac surrounding the heart. It can be caused by various conditions that obstruct fluid drainage or damage the pericardium, such as infection, malignancy, autoimmune diseases, or drugs. The document lists various infectious etiologies of pericardial effusion including bacteria, viruses, fungi, and protozoa. It also discusses non-infectious causes like cancer and connective tissue diseases. Routine testing of pericardial fluid includes cell count, glucose, protein and LDH levels to help determine the cause.
Leukopoiesis is the formation and maturation of white blood cells. It occurs primarily in the bone marrow through a series of mitosis and differentiation of stem cells into various white blood cell types. The major white blood cell types produced are granulocytes like neutrophils, eosinophils and basophils through granulopoiesis; monocytes through monocytopoiesis; and lymphocytes through lymphopoiesis. Leukopoiesis is regulated by growth factors and cytokines that influence the proliferation and specialization of stem cells in the bone marrow microenvironment.
Leukocytosis is an increase in the number of white blood cells. It occurs as part of the body's inflammatory response. The level of white blood cells is regulated by the rate of production and release from bone marrow and other storage sites, as well as the rate that cells exit the bloodstream into tissues. Leukocytosis can be caused by cytokines and growth factors that stimulate the differentiation and proliferation of specific white blood cell types, such as interleukin-5 for eosinophils and G-CSF for neutrophils. In severe inflammatory conditions, leukocytes may display abnormal morphologies including toxic granules, Dohle bodies, and cytoplasmic vacuoles.
This document provides an introduction to the field of pathology and laboratory medicine. It discusses the various careers available, including pathologists, medical laboratory scientists, and phlebotomy technicians. It also outlines the different departments in a medical laboratory, such as clinical chemistry, microbiology, and hematology. Key components of a complete blood count and different types of blood cells are defined. Abnormal blood cells and diseases like sickle cell anemia and leukemia are mentioned. Identification of microorganisms through gram staining is briefly introduced.
The document discusses leucocytes (white blood cells). It describes the classification of WBCs into granulocytes and agranulocytes. Granulocytes include neutrophils, eosinophils, and basophils which are involved in phagocytosis and immune responses. Agranulocytes include lymphocytes and monocytes. Lymphocytes provide humoral and cellular immunity while monocytes circulate in blood and differentiate into tissue macrophages. The reticuloendothelial system comprised of macrophages is also described which acts as a generalized phagocytic system in the body.
The document discusses hematopoiesis, the process of blood cell production. It describes how hematopoietic stem cells in the bone marrow differentiate into the various blood cell lineages through the action of growth factors. This includes erythropoiesis, granulopoiesis, megakaryopoiesis, and lymphopoiesis. It also covers reactive conditions that can cause changes in white blood cell counts, such as infections and inflammatory states.
The document provides information on differential leukocyte counting (DLC). It defines DLC as the relative proportion of different leukocytes expressed as a percentage. The main types of white blood cells (WBCs) described are granulocytes (neutrophils, eosinophils, basophils) and agranulocytes/mononuclear cells (lymphocytes, monocytes). Pathologic variations in DLC counts include neutrophilia, neutropenia, lymphocytosis, lymphopenia, monocytosis, eosinophilia, eosinopenia, and basophilia. Causes of each variation are outlined. Automated methods for differential counting are also discussed and compared to manual microscopic methods
This document discusses the analysis of blood components. It covers:
- The functions of blood including oxygen transport, waste removal, temperature regulation, and more.
- Types of blood testing done in hematology, immunology, blood banking, and chemistry sections.
- Components of a complete blood count including red blood cell count, white blood cell count, hemoglobin, hematocrit, and differential white blood cell count.
- The different blood cell types - red blood cells, white blood cells (granulocytes and agranulocytes), platelets, and their roles in the body.
- Procedures for examining blood smears and determining cell counts are also outlined.
This document discusses white blood cells (WBCs), also known as leukocytes. It begins with definitions of WBC and explains they help the body's defense mechanisms. It describes WBC composition and the normal total count range. It then classifies WBCs into granulocytes and agranulocytes and lists the types in each group. The document outlines the functions of neutrophils, monocytes, lymphocytes, eosinophils and basophils. It concludes with the method and calculation for determining total WBC count using a hemocytometer.
White blood cells, or leukocytes, are cells of the immune system that defend the body against infectious disease and foreign materials. There are five main types of leukocytes - granulocytes (neutrophils, basophils, eosinophils) and agranulocytes (lymphocytes, monocytes). Granulocytes contain granules that help them digest pathogens, while agranulocytes do not contain granules. Leukocytes are produced in the bone marrow and circulate throughout the body in blood and lymph fluid. An abnormal increase or decrease in the number of leukocytes can indicate certain diseases.
White blood cells have varying lifespans depending on their type. Granulocytes last 4-8 hours in circulation and a few more days in tissues. Monocytes last 10-20 hours in blood and months in tissues as macrophages. Lymphocytes circulate for weeks or months between lymphoid tissue, blood, tissues, and lymph before returning to blood. Disorders that can affect white blood cell counts include leucopenia from radiation or chemicals, and leukemias like lymphocytic or myelogenous leukemia, which can lead to infections, anemia, bleeding, and lack of energy.
This document discusses white blood cell disorders, focusing on quantitative disorders of the white blood cells. It describes leukocytosis, which is an increased number of white blood cells, and leukopenia, which is a decreased number. The main types of leukocytosis and leukopenia discussed are neutrophilic leukocytosis, lymphocytosis, and eosinophilia. The causes, pathophysiology, and clinical features of each of these conditions are explained in detail.
presented by HAFIZ M WASEEM
university of education LAHORE Pakistan
i am from mailsi vehari and studied in lahore
bsc in science college multan
msc from lahore
The document summarizes the major functions and components of blood. It discusses how blood transports oxygen, nutrients, hormones and removes waste products while regulating pH and temperature. Blood also protects the body through clotting and the immune response. The components of blood include red blood cells, white blood cells, platelets and plasma. Abnormalities can cause issues like anemia or clotting disorders.
acute leukemia
For More Medicine Free PPT - http://playnever.blogspot.com/
For Health benefits and medicine videos Subscribe youtube channel - https://www.youtube.com/playlist?list=PLKg-H-sMh9G01zEg4YpndngXODW2bq92w
This document provides information about acute lymphoblastic leukemia (ALL). It discusses that ALL is a cancer of the lymphoid cells that is most common in children. The document covers the classification, immunologic subtypes, cytogenetic abnormalities, clinical features, diagnostic measures, and hematological and histological findings of ALL. It describes that ALL is diagnosed based on complete blood count, peripheral smear, bone marrow biopsy and cytogenetic/flow cytometry analysis. The key diagnostic findings include anemia, leukocytosis, thrombocytopenia and lymphoblasts in the bone marrow.
This document discusses various laboratory investigations used in oral and maxillofacial surgery (OMFS). It describes hematological tests including complete blood count, red blood cell indices, platelet count, and bleeding time. It outlines normal ranges and clinical implications of increased or decreased results for hematological parameters. These laboratory tests provide important information to establish medical diagnoses and guide patient management in OMFS.
This document provides information on white blood cell disorders, including qualitative and quantitative disorders. It discusses Chediak-Higashi syndrome, a rare autosomal recessive disorder characterized by abnormal granules in neutrophils resulting in decreased immune function. Leukemia is summarized as a malignant disorder of stem cells associated with increased white cells in bone marrow and blood. The classification, clinical features, investigations and management of acute leukemia are outlined.
Chronic lymphocytic leukemia (CLL) is the most common type of leukemia in adults. It has an average incidence of 2.7 per 100,000 people in the US and is more common in older men. CLL accounts for about 0.8% of all cancers and 30% of leukemias. The neoplastic cells are typically B-cell lymphocytes. Farming exposure and hepatitis C may play a role in etiology. CLL has various genetic abnormalities that affect prognosis. Clinical features include lymphadenopathy, fatigue, infections. Diagnosis requires a sustained lymphocytosis above 5000/uL. Treatment is indicated for symptomatic disease, doubling time under 6 months, or disease complications. Prognostic factors
Acute leukemias are clonal malignant disorders characterized by the accumulation of immature blast cells in the bone marrow, which replaces normal marrow tissue. This results in bone marrow failure and peripheral blood cytopenias. Acute leukemias are classified as either acute lymphoblastic leukemia (ALL) or acute myeloid leukemia (AML) based on the affected cell lineage. Treatment involves intensive chemotherapy aimed at inducing remission followed by consolidation therapy to eradicate residual leukemia cells. Supportive care is also important to manage complications such as infection during treatment. Long term side effects can include second malignancies, organ dysfunction, and infertility. Prognosis depends on factors like age, white blood cell count, and response to initial
This document discusses leukemia, which are cancers of the white blood cells. It describes the main types of leukemia - acute and chronic forms of myeloid and lymphoblastic leukemia. Acute leukemias involve immature white blood cells while chronic leukemias involve more mature cells. The most common chronic leukemia is chronic myeloid leukemia, which results from a genetic abnormality known as the Philadelphia chromosome. Signs, symptoms, diagnosis and treatment of acute myeloid leukemia and chronic myeloid leukemia are summarized.
Acute myeloid leukemia (AML) is a cancer of the blood and bone marrow characterized by increased proliferation of immature blast cells. It results from mutations that affect the common myeloid progenitor cell. Symptoms include fatigue, fever, bleeding, and infections. Diagnosis involves blood and bone marrow tests showing elevated white blood cell counts with immature blasts. Standard treatment is 7-day continuous cytarabine with 3-day daunorubicin induction chemotherapy, with hematopoietic stem cell transplant for high risk cases. Prognosis depends on risk factors like age and genetic abnormalities.
This document summarizes information about cryoglobulinemic vasculitis. It defines cryoglobulins as immunoglobulins that precipitate out of solution at low temperatures. Cryoglobulinemic vasculitis is caused by immune complex-mediated small to medium vessel inflammation from cryoglobulin containing immune complexes. It most often presents with palpable purpura, arthralgias, and signs of vascular occlusion. Diagnosis involves identifying elevated cryoglobulins and signs of vasculitis on biopsy. Treatment focuses on immunosuppression and treating underlying infections or diseases that may be contributing.
The document discusses abnormalities of white blood cells, including quantitative abnormalities like leukocytosis and leukopenia as well as qualitative abnormalities involving the nucleus or cytoplasm of white blood cells. Some examples of qualitative abnormalities discussed include Pelger-Huet anomaly, Chediak-Steinbrinck-Higashi syndrome, and Auer rods. The types of white blood cells are described along with causes of conditions like neutrophilia, eosinophilia, lymphocytosis, and monocytosis. Inherited and acquired morphological and functional abnormalities of white blood cells are also summarized.
This document provides an overview of acute and chronic leukemia. It defines leukemia as a group of malignant disorders affecting blood and blood-forming tissues. It discusses the main types of acute leukemia - acute lymphoblastic leukemia and acute myeloid leukemia. It covers the causes, symptoms, types and treatment for each. It also defines chronic leukemia and discusses chronic lymphocytic leukemia and chronic myelogenous leukemia in more detail including their pathophysiology, stages, risk factors, clinical presentation and treatment options.
This document provides an overview of leukemia, including its definition, types, causes, symptoms, diagnosis, and treatment. Leukemia is a cancer of the blood and bone marrow characterized by abnormal blood cell production. There are four main types classified by cell type and disease progression: acute or chronic, myeloid or lymphoid. Causes are often genetic defects or environmental exposures. Symptoms vary by type but can include fatigue, infections, bruising, and organ enlargement. Diagnosis involves blood and bone marrow tests. Treatment aims to cure or control the disease using chemotherapy, radiation, stem cell transplants, and supportive care.
Leukemia is a malignant disease characterized by the replacement of normal bone marrow elements with abnormal blood cells. The document discusses the history, etiology, pathogenesis, classification, clinical features, laboratory findings, treatment and oral manifestations of various types of leukemia including chronic myeloid leukemia (CML), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), and acute lymphoblastic leukemia (ALL). Guidelines for dental treatment and management of patients with leukemia during different phases of disease and therapy are also provided.
All ACUTE LYMPHOBLASTIC LEUKEMIA BY DR MAGDI SASIcardilogy
1. The document provides information about acute lymphocytic leukemia (ALL), the most common type of cancer in children. It describes the symptoms, signs, classification, and risk factors of ALL.
2. Common symptoms of ALL include fever, fatigue, easy bruising, frequent infections, and bone/joint pain. Physical signs may include pallor, organ enlargement, and lymphadenopathy.
3. ALL is classified according to the type of lymphocytes involved (B-cell vs T-cell lineage) and cellular features. The vast majority of ALL cases involve B-cell lymphocytes. Risk factors for ALL are generally unknown for most people.
This document provides an overview of 10 topics related to blood:
1. The composition and components of blood including erythrocytes, leukocytes, and platelets.
2. Erythropoiesis, the production and degradation of red blood cells.
3. The immune system including humoral and cellular immunity.
4. Blood groups such as ABO and Rh and issues like blood typing and transfusion reactions.
5. Hemostasis, the process of blood clotting and fibrinolysis.
This document discusses atypical lymphocytes and lymphocyte disorders. It begins by describing different types of normal and reactive lymphocytes seen in non-malignant conditions like viral infections. It then discusses acquired and congenital causes of lymphocytosis and lymphopenia. Malignant lymphocyte disorders covered include various leukemias and lymphomas. Key information provided includes morphological features of different lymphocyte cell types, immunophenotyping results, and clinical correlates that can help distinguish reactive from malignant processes.
This document discusses acute myeloid leukemia (AML) and its acute complications. It defines AML as a clonal expansion of myeloid precursor cells with reduced capacity to differentiate. Common clinical presentations include fever, bleeding, and fatigue due to excessive proliferation of myeloid cells in the bone marrow leading to pancytopenia. Two major acute complications discussed are leukostasis, which can cause pulmonary and neurological symptoms, and tumor lysis syndrome, which results in electrolyte abnormalities and renal impairment.
Leukocytosis is an increased white blood cell count in the blood. There are five main types: neutrophilia, lymphocytosis, monocytosis, eosinophilia, and basophilia. Neutrophilia is most common and usually due to bacterial infection. Eosinophilia can be caused by allergic disorders, parasites, and some cancers. Lymphocytosis is seen with viral infections and lymphomas. Leukopenia and neutropenia involve decreased white blood cell and neutrophil counts respectively, increasing infection risk. Lymphoma involves abnormal lymphocyte proliferation. Leukemia includes acute and chronic forms, with acute being more aggressive and involving immature cells.
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This document discusses flow cytometry and its application in cancer diagnosis and molecular testing. It provides details on several tests performed using flow cytometry, including immunophenotyping for different types of leukemia and lymphoma. It also discusses the classification of acute leukemias according to the FAB and WHO systems and provides information on different FAB subtypes of acute myeloid leukemia such as M0, M1, M2, M3, M4, and M5. The document aims to inform clinicians on the diagnostic and clinical utility of various flow cytometry tests.
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
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These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...Donc Test
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8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
2. Learning objectives
✓ Recognize the different types of leucocytes
(myeloid cells & lympoid cells).
✓ List the normal values for neutrophils,
eosinophils, basophils, and monocytes in
normal peripheral blood
✓ Be familiar with terms of leukoerythroblastic
picture and leukemoid reaction
✓ Identify conditions that cause increase or
decrease for each of them.
2WaseemTameemi
3. The white blood cells
(leucocytes):
Phagocytes
innate immune system,
1. Granulocytes: (neutrophils,
eosinophils , basophils) and
2. monocytes
Lymphocytes
adaptive immune response,
WaseemTameemi 3
4. Leucocyte
Mediate host defense
Modulate the immune response
The relative proportion
The absolute number
―ANC‖—absolute neutrophil count
– Philia, – cytosis
– Penia
WaseemTameemi 4
8. Neutrophils
maturation within 5 days in BM
stay 6-10 hours in the circulation
before being removed, mainly by
the spleen.
Myeloblast, promyelocyte,
Myelocytes or metamyelocytes are
normally only found in the marrow
if appear in the circulation :
infection or neoplastic states or
BM stimulation.
WaseemTameemi 8
12. Leukoerythroblastic reaction
a serious disturbance of marrow function
The WBC count may be increased,
normal, or decreased
BM metastasis
MF
Leukemia (AML,CML)
MM
Reactive states ( hemorrhage or hemolysis )
Corticosteroid therapy
Indication of bone marrow study
WaseemTameemi 12
13. Neutrophils
the most common white
blood cells in the blood
of adults.
approximately 65 %
2-5 segments nuclei
and granules in their
cytoplasm.
13WaseemTameemi
18. Leukemoid reaction
Benign leukocytic proliferation
a significant increase in immature
precursors in the peripheral blood
(myeloblast, myelocytes,
metamyelocytes, band) along with
increased numbers of mature forms.
DDX: acute or chronic leukemia
Severe infection, metastatic cancer,
hemolysis, burn.
WaseemTameemi 18
19. Eosinophils
represent 1-6% of
the circulating WBC.
involved in
intracellular killing of
protozoa and
helminths
allergic reactions
(e.g. atopy, asthma)
19WaseemTameemi
22. Basophils
Less than 1% of WBC.
Mast cells resemble
basophils (only found
in the tissues).
They release histamine
type I hypersensitivity
reaction and
defense against parasites
22WaseemTameemi
25. Monocytes
Main functions of macrophages:
1) Phagocytosis.
2) Facilitate wound healing.
3) Removal of senescent RBCs in
reticuloendothelial system
(spleen, liver and bone marrow).
4) Presentation of antigen to T
lymphocytes.
WaseemTameemi 25
27. Lymphocytes
T cells (80% of circulating
lymphoid cells)
B cells
expression of immunoglobulin
light chains
lifespan can vary from several
days to many years.
27WaseemTameemi
28. Lymphocytic leukocytosis
>> 3,500/mm³
( 3.5 X109/L )
infections such as viral;
(infectious mononucleosis
,mumps , measles) and
bacterial; (pertussis, TB)
lymphoproliferative disorders:
acute and chronic lymphocytic
leukemias, lymphoma
post splenectomy
28WaseemTameemi
29. Neutropenia
< 1500/mm³. (1.5 X109/L)
< 500/mm³ (0.5 X109/L)
Agranulocytosis : neutropenia
recurrent infections
Bone marrow examination
less than 0.2 × 109/L
very serious
Very significant risk of infection; fever should
always be managed on an inpatient basis with
parenteral antibiotics; few or no clinical signs of
infection
29WaseemTameemi
30. The clinical features of
neutropenia:
risk of infection, at the mouth and
throat.
Painful necrotizing ulcers on oral
cavity , the anus and skin (boil,
abscess)
The general symptoms :fever, chills,
malaise, weakness and fatigability.
Septicaemia
the infection will be severe & life threatening
within hours to few days
30WaseemTameemi
31. The clinical features of
neutropenia:
Commensal by normal
individuals may become
pathogens.
(Staphylococcus epidermidis or
Gram‐negative organisms in the bowel)
Candida and Aspergillus.
Invasive bacterial or fungal infections
may occur in the organs like GIT, lungs
and urinary tract.
31WaseemTameemi
32. Neutropenia
1. infections:
Flu,Hepatitis B virus, Epstein-Barr virus and
HIV
Enteric fever, brucellosis, and tuberculosis
Malaria
2. Drugs: cytotoxic, carbimazole, sulphasalazine,
trimethoprim, carbamazapines,
3. Auto immune:SLE, Felty’s syndrome
4. Congenital: Kostmann’s syndrome,
Schwachman–Diamond
5. acute leukemia
6. bone marrow failure or infiltration
32WaseemTameemi