Polycythaemia is a blood disorder that results in an increased level
of circulating red blood cells in the blood stream. Polycythaemia
usually means an increase in haematocrit (the ratio of the volume of red
blood cells to the total volume of blood) and haemoglobin (the protein
responsible for transporting oxygen in the blood). Polycythaemia occurs
when the haematocrit is greater than 48% in women and 52% in men and/or
the haemoglobin level is greater than 16.5g/dL (gram per decalitre) in
women and 18.5g/dL in men. There are two types of polycythaemia, Primary
polycythaemia, which is due to inherent problems in red blood cell
production, and Secondary polycythaemia which occurs as a response to
other factors or underlying conditions that promote red blood cell
production.
Symptoms
Symptoms of polycythaemia may vary among people, with some having minimal to no symptoms. However, the common and general symptoms include:
Causes
Causes of polycythaemia are primary and secondary, just like its types. Here are details:
Primary Polycythaemia
Primary polycythaemia occurs due to acquired or inherited genetic mutations, and have two sub-types, which include:
Secondary polycythaemia is usually caused by increased erythropoietin in response to chronic hypoxia (low oxygen levels) or an erythropoietin secreting tumour.
o Chronic heart diseases
o Sleep apnoea
o Pulmonary hypertension
o Kidney Cancer
o Adrenal adenoma
o Uterine tumours
Symptoms
Symptoms of polycythaemia may vary among people, with some having minimal to no symptoms. However, the common and general symptoms include:
- Weakness
- Fatigue
- Headache
- Itching
- Easy bruising
- Joint pain
- Dizziness
- Abdominal pain
Causes
Causes of polycythaemia are primary and secondary, just like its types. Here are details:
Primary Polycythaemia
Primary polycythaemia occurs due to acquired or inherited genetic mutations, and have two sub-types, which include:
- Polycythaemia Vera: This is a rare condition typically associated with an elevated white blood cell count and platelet count, known as leucocytosis and thrombocytosis respectively. An enlarged spleen is a distinct clinical feature of polycythaemia Vera.
- Primary Familial and Congenital Polycythaemia (PFCP): This type is also thought to be caused by genetic mutations to the EPOR gene which provides instructions to make erythropoietin, which is the hormone responsible for red blood cell production.
Secondary polycythaemia is usually caused by increased erythropoietin in response to chronic hypoxia (low oxygen levels) or an erythropoietin secreting tumour.
- Chronic hypoxia is in turn caused by chronic lung diseases such as:
o Chronic heart diseases
o Sleep apnoea
o Pulmonary hypertension
- Erythropoietin secreting tumours can release increased amount of erythropoietin. The most common of these are:
o Kidney Cancer
o Adrenal adenoma
o Uterine tumours