week 10 Flashcards

blood disorders and workshop 5

1
Q

Erythrocytes function

A

= increase oxygen diffusion, Haemoglobin

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1
Q
  • Describe blood components
A
  • Erythrocytes; Non-nucleated (RBC)
  • Leukocytes; have nucleus usually the largest cell type of coloured purple
  • platelets; non-nucleated (small)
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2
Q

Erythrocytes Disorders

A
  1. Anaemia= <Haemoglobin concentration or reduction in haematocrit
    2.Polycythaemia = Increase in RBC concentration
    * Increase in haemoglobin
    * Increase in haematocrit
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3
Q

Anaemia caused by

A

Decrease in MCV
* Decrease in MCH
Genetic and acquired forms of Anaemia.

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4
Q

common types of anaemia

A

Common
* Anisocytosis = variation in RBC size
* Poikilocytosis = abnormal shape RBC

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5
Q

Anaemia refers to

A

anaemia refers to a reduction in hemoglobin concentration in the blood, leading to decreased oxygen-carrying capacity.

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6
Q

symptoms of anemia include

A

Increased heart rate
Fatigue, weakness
Pallor of the skin
Headaches and mild fever

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7
Q

causes of anaemia

A

Causes of anemia include blood loss, decreased red blood cell production, or increased red blood cell destruction​

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8
Q

Normal Erythrocyte Diagnostics:

A

Mean Corpuscular Volume (MCV): Measures the average size of red blood cells. Normal range in adults: 80-96 fL/red cell.
Mean Corpuscular Hemoglobin (MCH): Amount of hemoglobin per red cell. Normal range in adults: 27-33 picograms (pg)/cell.
Mean Corpuscular Hemoglobin Concentration (MCHC): Concentration of hemoglobin in a given volume of packed red cells. Normal range in adults: 33-36 g/d

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9
Q

General Anaemia Classifications:

A

Microcytic/Hypochromic Anemia:
Characterized by smaller-than-normal red cells (low MCV) and reduced hemoglobin (low MCH).
Common causes: iron deficiency, thalassemia.
Macrocytic Anemia:
Characterized by larger-than-normal red cells (high MCV).
Common causes: Vitamin B12 or folate deficiency (megaloblastic anemia).
Normocytic/Normochromic Anemia:
Red cells are of normal size and hemoglobin content but reduced in number.
Causes: acute blood loss, bone marrow failure, most hemolytic anemias

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10
Q

Cellular Anaemic Variants:

A

Iron Deficiency Anemia: Causes hypochromic microcytic red cells (pale, small RBCs).
Megaloblastic Anemia: Due to Vitamin B12 or folate deficiency; causes macrocytic red cells (larger RBCs).
Sickle Cell Anemia: Inherited form that results in sickle-shaped red cells under low oxygen conditions. Causes chronic hemolytic anemia and vaso-occlusion.
Thalassemia: Genetic disorder affecting hemoglobin synthesis, resulting in microcytic hypochromic anemia.
Hereditary Spherocytosis: Red cells are spherical and lack deformability, leading to their premature destruction in the spleen

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11
Q

whats this?

A

Hypochromic microcytic anaemia of iron deficiency. Hypochromic refers to red blood cells (RBCs) that have less hemoglobin than normal, resulting in a pale appearance. Microcytic refers to smaller-than-normal RBCs, which is characteristic of iron deficiency anemia.
The RBCs in the image appear both pale (due to reduced hemoglobin content) and small, which are hallmarks of iron deficiency.

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12
Q

Anemia causes a reduction in….

A

the blood’s oxygen-carrying capacity.

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13
Q

Three Classifications of Anemia:

A

Dyshaemopoietic Anemia: Caused by production failure (e.g., iron deficiency, vitamin B12 deficiency).
Haemorrhagic Anemia: Caused by excessive blood loss.
Haemolytic Anemia: Caused by excessive destruction of RBCs​

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14
Q

whats this

A
  • Dyshaemopoietic
    (Production failure)
    Anaemias, specifically iron deficiency anemia the most common cause of anaemia.
  • Iron Deficiency Anemia leads to the production of microcytic (small) and hypochromic (pale) red blood cells. This is due to a lack of sufficient iron needed for hemoglobin production.
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15
Q

Causes of iron deficiency anemia include

A

Increased requirements (e.g., pregnancy, growth spurts)
Malabsorption (e.g., conditions that reduce iron absorption like celiac disease)
Malnutrition (poor dietary intake of iron)

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16
Q

what is this?

A

This image highlights various Dyshaemopoietic (Production Failure) Anemias, particularly those related to Vitamin B12, folate deficiency, and Pernicious Anaemia. Histological feature: Hypersegmented neutrophils, which are a hallmark of megaloblastic anemia.

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17
Q

causes of Vitamin B12 and Folate Deficiency Anemia:

A

Causes include:
Gastrectomy (removal of part of the stomach reduces absorption)
Congenital lack of intrinsic factor (necessary for B12 absorption)
Crohn’s Disease (affects nutrient absorption in the intestines)
Malnutrition

18
Q

what is Pernicious Anemia:?

A

A type of B12 deficiency anemia caused by a severe or total lack of intrinsic factor secretion.
This condition leads to poor B12 absorption and requires lifelong B12 replacement therapy.
Prognosis is poor without treatment.

19
Q

Other Dyshaemopoietic Anemias:

A

Folate deficiency anemia: Clinically similar to pernicious anemia but caused by folate deficiency rather than B12.
Aplastic anemia: Failure of bone marrow to produce enough blood cells. It can be primary (rare) or secondary.
Toxic dyshaemopoietic anemia: Anemia caused by exposure to toxins.
Leucoerythroblastic anemia: Caused by a space-occupying lesion in the bone marrow, leading to crowding out of normal hematopoiesis

20
Q

whats this

A
  • This image shows spherocytes, which are red blood cells that appear round and lack the normal biconcave shape. This is characteristic of hereditary spherocytosis, a type of hemolytic anemia.
  • This condition is caused by a defect in the erythrocyte membrane proteins, particularly spectrin or ankyrin, leading to membrane instability.
  • Splenectomy is often performed in severe cases to reduce the hemolysis and anemi
21
Q

Haemorrhagic Anemias

A

= acute (>1500ml is bad) or chronic blood loss (from ulcers and hemmorrhoids or malignant tumours)

22
Q

Haemolytic Anemias-Sickle Cell Anemia cause?

A

Caused by a homozygous inherited mutation in the gene for hemoglobin. Under low oxygen tension, the variant hemoglobin crystallizes, causing chronic hemolytic anemia and microvascular occlusion.
Bone marrow becomes hyperplastic, and there is early splenomegaly in childhood, followed by a shrinking spleen due to vascular occlusion.

23
Q

Thalassemia is

A

Genetic disorder affecting alpha or beta globin chain synthesis.Thalassemia major causes severe microcytic hypochromic anemia, with bone marrow hyperplasia, cortical bone thinning, and enlargement of the liver and spleen (extramedullary erythropoiesis).
Results in severe anemia, growth retardation, and failure of sexual development.

24
Q

Acquired Haemolytic Anemias caused by?

A

Caused by conditions such as malaria, autoimmune anemias, and toxic anemias.

25
Q

Malaria causes

A

Damaged red blood cells become sticky, leading to anemia and microthrombi.
Symptoms include cyclic fevers and chills, hepatosplenomegaly, jaundice, and kidney damage due to the sudden rupture of a large number of erythrocytes.

26
Q

what are polycythaemias:?

A

Primary Polycythemia: Possibly neoplastic in nature, with abnormal sensitivity to erythropoietin.
Secondary Polycythemia: Caused by conditions like high altitude (stimulating bone marrow hyperplasia) or cardiovascular diseases (like COPD), leading to compensatory increases in red cell production.
Results in increased blood viscosity, which can cause skin congestion, nosebleeds, hypertension, splenomegaly, and thrombosis​

27
Q

what are Leukocytes?

A

WBC, for defence, 5 types: Neutrophil (granulocytes)
* Lymphocytes
* Monocytes
* Eosinophil (granulocytes)
* Basophil (granulocytes) (most to least abundant)

28
Q

what is this?

A

Neutrophils
* Most abundant WBC
* Granulated – enzymes, lysozymes
* Spend 14 days in bone marrow
* Neutrophil half life is 6-9 hours
* Therefore peripheral neutrophils only 10% of all neutrophils

29
Q

whats this?

A

Lymphocytes
Large round nucleus
* T and B forms
* Stimulate and regulate the immune system

30
Q

this?

A

Monocytes
* Largest
* Curved, single lobed nucleus
* Similar function to neutrophil
* Enter tissue
* Form macrophage
* Phagocytose

31
Q
A

Eosinophil
* Large red granules
* Lobulated nucleus
* Important in mediating allergy
* Defence against parasites

32
Q

What’s this

A

Basophil
* Least abundant
* Large blue/black granules obscure nucleus
* Contain Heparin and histamine
* Involved in hypersensitivity
* Act like mast cells

33
Q

what is this?

A

qualitative leukocyte disorders, specifically focusing on hypersegmented neutrophils and toxic granulation.
Key Features in the Image:
Hypersegmented Neutrophils: These are neutrophils with more than the normal number of nuclear segments (typically 6 or more lobes), often seen in megaloblastic anemia (due to vitamin B12 or folate deficiency).
Toxic Granulation: This refers to the presence of dark, coarse granules in the cytoplasm of neutrophils, which can occur during severe infections or inflammatory conditions, such as sepsis.

34
Q

what are Leukocyte Disorders?

A

has Quantitative vs Qualitative changes. Quantitative
* Leukocytosis = increase number
* Eg. Monocytosis, eosinophil leucocytosis
* Leukopenia = decrease in number
* Eg. Overwhelming sepsis, autoimmune diseases, drug induced. Qualitative
* Changes in phagocyte cell function
* Hypersegmented neutrophils
* Toxic granulation

35
Q

what is this

A

This image likely represents a bone marrow aspirate or peripheral blood smear in a case of leukemia or another bone marrow disorder. The image shows:

Numerous abnormal cells: Large cells with abnormal nuclear-to-cytoplasmic ratios, including blasts (immature white blood cells), which are typical in leukemias.
Prominent purple-stained nuclei in many of the cells, which suggests the presence of immature or neoplastic leukocytes.
Increased cellularity: There appears to be a significant number of white blood cells, possibly indicating a proliferative disorder such as acute leukemia.

36
Q

Platelet Disorders

A
  • Deficiency = thrombocytopenia
  • Spontaneous bleeding
  • Increase = thrombocytosis
  • Due to = blood loss, iron deficiency, trauma, inflammatory conditions
37
Q

What is the clinical term used to describe the radiating pain?

A

Referred angina

38
Q

What does diaphoresis mean?

A

Profuse sweating

39
Q

A 45-year-old man was awakened by chest pain that radiated to both arms and neck and
was associated with diaphoresis. His blood pressure was 160/110. He was treated with diuretics (Lasix). He
developed a friction rub. Two days after the onset of the chest pain he had a cardiac arrest and died. what condition did he likely have? and The event MOST LIKELY associated with
this patient’s problem was:

A

Occlusion of a coronary artery. Occlusive thrombus

40
Q

treating with diuretics.=

A

Decrease BP

41
Q

What is a transmural infarct?

A

Infarct spanning whole thickness of heart wall.

42
Q

Give 3 abnormal features of the
myocardium pictured:

A

Coagulative Necrosis: The myocardial fibers appear wavy and lack nuclei, which indicates coagulative necrosis due to ischemia. This is typical of myocardial infarction (MI) within the first 24-48 hours after the ischemic event.

Neutrophil Infiltration: There is a visible infiltration of neutrophils between the muscle fibers, which is a hallmark of acute inflammation in response to tissue injury, commonly seen in the early stages of MI (1-3 days after onset).

Loss of Cellular Detail: The myocardial cells show loss of distinct striations and structural integrity, which is another feature of ischemic damage, as the cells lose their ability to maintain their normal morphology due to the lack of oxygen and nutrients.

These findings are consistent with the early stages of a myocardial infarction and reflect the inflammatory response and tissue damage caused by the lack of blood supply to the heart muscle.