Polycythemia vera (NORD)

Polycythemia vera (NORD)

Core Conditions

Core Conditions

Plasmodium species (Malaria)
Antimalarials
HIV and AIDS: Pathology review
Testicular cancer
Testicular and scrotal conditions: Pathology review
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Heart failure: Pathology review
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Eye conditions: Refractive errors, lens disorders and glaucoma: Pathology review
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Eye conditions: Retinal disorders: Pathology review
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Ascending and descending spinal tracts
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Typical antipsychotics
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Back pain: Pathology review
Anatomy clinical correlates: Bones, joints and muscles of the back
Osteoporosis
Osteoporosis: Clinical sciences
Osteoporosis medications
Bones of the vertebral column
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Vessels and nerves of the vertebral column
Muscles of the back
Cauda equina syndrome
Blood groups and transfusions
Blood products and transfusion: Clinical
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Approach to hypertensive disorders in pregnancy: Clinical sciences
Preeclampsia & eclampsia
Aortic dissections and aneurysms: Pathology review
Aortic dissection
Aortic aneurysms and dissections: Clinical
Aortic dissection: Clinical sciences
Abdominal aortic aneurysm: Clinical sciences
Epstein-Barr virus (Infectious mononucleosis)
Leukemias: Pathology review
Acute leukemia
Complement system
Immune thrombocytopenia
Heparin-induced thrombocytopenia
Thrombotic thrombocytopenic purpura
Essential thrombocythemia (NORD)
Systemic lupus erythematosus
Systemic lupus erythematosus: Clinical sciences
Antiphospholipid syndrome
Treponema pallidum (Syphilis)
Fever of unknown origin: Clinical
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Anal cancer: Clinical sciences
Thyroid cancer
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Hepatitis C: Clinical sciences
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Hepatitis A and E: Clinical sciences
Viral hepatitis: Clinical
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Cushing syndrome
Graves disease
Chronic leukemia
Non-Hodgkin lymphoma
Hodgkin lymphoma
Stroke: Clinical
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Subarachnoid hemorrhage
Intracerebral hemorrhage
Gallbladder disorders: Pathology review
Approach to biliary colic: Clinical sciences
Biliary colic
Gallstone ileus
Anaphylaxis: Clinical sciences
Community-acquired pneumonia: Clinical sciences
Malaria: Clinical sciences
Sepsis: Clinical sciences
Approach to shock: Clinical sciences
Polymyalgia rheumatica
Rheumatoid arthritis
Measles virus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Hyponatremia
Electrolyte disturbances: Pathology review
Hyperkalemia
Hypercalcemia
Hypokalemia
Hypernatremia
Vasculitis: Pathology review
Vasculitis
Lymphomas: Pathology review
Myelodysplastic syndromes
Polycythemia vera (NORD)
Pulmonary transfusion reactions: Clinical sciences
Kawasaki disease
Upper respiratory tract infection
Febrile neutropenia: Clinical sciences
Severe chronic neutropenia (NORD)
Approach to postoperative respiratory distress: Clinical sciences
Approach to a postoperative fever: Clinical sciences
Atelectasis: Clinical sciences
Pleural effusion, pneumothorax, hemothorax and atelectasis: Pathology review
Cystic fibrosis
Cystic fibrosis: Pathology review
Dyslipidemias: Pathology review
Hyperthyroidism
Hypothyroidism: Pathology review
Hyperthyroidism: Pathology review
Hypothyroidism
Laryngitis
Nasal polyps
Diabetes insipidus and SIADH: Pathology review

Transcript

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In polycythemia vera, there are increased blood cell levels due to overproduction by the bone marrow, which is a soft tissue found within the bones.

Normally, about 45% of the total blood volume is made up of erythrocytes, or red blood cells, and their main function is to carry oxygen to tissues and bring carbon dioxide to the lungs so it can be expired. This value is called the hematocrit.

In polycythemia vera there’s an increase in red blood cell production.

It typically begins with a mutation in a single hematopoietic stem cell, which gives rise to red blood cells, white blood cells, and platelets.

In 90 percent of the affected individuals there is a mutation of the Janus Kinase 2 or JAK2 gene.

Normally, the kidneys produce erythropoietin which is a hormone that binds to receptors on the hematopoietic stem cells and activates JAK2 gene.

When that happens, it causes the cell to divide and thus produce more blood cells.

However, when there’s a mutation, it keeps JAK2 gene activated, and these cells are able to divide even in the absence of erythropoietin.

The mutated cells proliferate, and rapidly become the predominant hematopoietic cells in the bone marrow.

In time these cells start to die out and that’s when scar tissue forms.

At that point, the bone marrow can no longer produce blood cells, leading to anemia or low red blood cell levels, thrombocytopenia or low platelet levels, and leukopenia or low white blood cell levels. This is known as the spent phase.

And once the disease is in the spent phase, it’s really a different disease altogether - at that point it’s myelofibrosis.

The most common symptoms of polycythemia vera are fatigue, dizziness, increased sweating, redness in the face, blurred vision, and itchy skin especially after a hot shower.

Itchiness develops due to the increased number of basophils and mast cells which contain histamine that causes itching when released.

Splenomegaly or spleen enlargement is also common because the excess red blood cells buildup in the spleen, which usually helps with removing excess cells.

High turnover of red blood cells can cause build up of uric acid which leads to the inflammation of joints or gout and kidney stones.

Key Takeaways

Polycythemia vera is a bone marrow disorder in which there is an overproduction of blood cells, often caused by a JAK2 mutation within hematopoietic cells in the bone marrow. It can lead to elevated hemoglobin and hematocrit and predispose an individual to develop blood clots. Symptoms may include fatigue, weakness, headaches, dizziness, itching, and abdominal pain. Treatment may include medications to lower blood cell formation, and prevention of blood clots, phlebotomy, and radiation therapy.