Blood Disease Definitions Flashcards

Basic Definitions of Blood Diseases with some signs and symptoms.

1
Q

Anemia Due to Blood Loss

A
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Microcytic Anemia

A

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).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Normochromic-normocytic Anemia

A

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)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Macrocytic Anemia

A

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.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Anemia S/S

A
Symptoms include:
● Tiredness. ● Lightheadedness. ●
coexisting disease, e.g. angina.
Signs include:
● Mucous membrane pallor. ● murmurs. ● Ankle oedema. ●Tachypnoea. ● Raised JVP. ● Postural hypotension. ●tachycardia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Leucopenia

A

low WBC count

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Leucocytosis

A

high WBC count

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Neutrophilia Causes

A

High Neutrophil Count: Infection. ● Trauma. ● Myocardial infarction (MI). ●Inflammation ● Malignancy. ● Myeloproliferative disorders.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Lymphocytosis

A

High Lymph count; Most commonly seen in viral infections

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Eosinophilia

A

High Eosinophil Count; Allergy ( asthma, drug reactions etc.), Parasitic Infections; Inflammatory Disease; Malignancy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Lymphadenopathy

A

Enlarged Lymph Nodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Splenomegaly

A

Enlarged Spleen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Thrombocytopenia

A

Low Platelet Count

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Thrombocytosis

A

High Platelet Count

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Megaloblastic anaemia

A

This results from deficiency of vitamin B12

or folic acid, both of which are required for DNA synthesis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Pernicious anaemia

A

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.

17
Q

Haemolytic anaemia

A

When destruction exceeds production, haemolytic anaemia results

18
Q

Sickle-cell anaemia

A

When HbS is deoxygenated, the Hb molecules polymerise and the red cell membrane becomes distorted, producing characteristic sickle-shaped cells

19
Q

thalassaemias

A

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.

20
Q

Leukemias

A

Leukaemias are malignant disorders of haematopoietic stem cells, associated with increased numbers of white cells in the bone marrow and/or peripheral blood

21
Q

Types of Leukemias

A

Acute lymphoblastic leukaemia (ALL).(most common in children) ●
(AML). ● Chronic lymphocytic leukaemia (CLL). ● leukaemia (CML)

22
Q

Acute Leukemias

A

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

23
Q

Most Common Type of Leukemia

A

Chronic lymphocytic leukaemia (CLL) is the most common variety of leukaemia, typically presenting between the ages of 65 and 70 yrs.

24
Q

Cytopenia

A

Cytopenia is a reduction in the number of mature blood cells.

25
Q

Hodgkin lymphomas

A

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)

26
Q

Non-Hodgkin lymphomas (NHL)

A

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)

27
Q

Multiple myeloma

A

This is a malignant proliferation of plasma cells and has a peak incidence between the ages of 60 and 70 yrs

28
Q

aplastic anaemia

A

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

29
Q

erythropoiesis

A

production of RBCs