Paroxysmal nocturnal hemoglobinuria (patient information)
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| Paroxysmal nocturnal hemoglobinuria (patient information) | |
| ICD-10 | D59.5 |
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| ICD-9 | 283.2 |
| OMIM | 311770 |
| DiseasesDB | 9688 |
| MedlinePlus | 000534 |
| MeSH | D006457 |
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Paroxysmal nocturnal hemoglobinuria |
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Where to find medical care for Paroxysmal nocturnal hemoglobinuria? |
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Paroxysmal nocturnal hemoglobinuria On the Web |
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Directions to Hospitals Treating Paroxysmal nocturnal hemoglobinuria |
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Risk calculators and risk factors for Paroxysmal nocturnal hemoglobinuria |
Editor-in-Chief: C. Michael Gibson, M.S.,M.D. [1] Phone:617-632-7753; Associate Editor-In-Chief: Lakshmi Gopalakrishnan, M.B.B.S.
Overview
Paroxysmal nocturnal hemoglobinuria is a rare disease in which red blood cells break down earlier than normal.
What are the symptoms of Paroxysmal nocturnal hemoglobinuria?
- Abdominal pain
- Back pain
- Blood clots may form in some people
- Dark urine: comes and goes
- Easy bruising or bleeding
- Headache
- Shortness of breath
What causes Paroxysmal nocturnal hemoglobinuria?
- Persons with this disease have blood cells that are missing a gene called PIG-A. This gene allows a substance called glycosyl-phosphatidylinositol (GPI) to help certain proteins stick to cells.
- Without PIG-A, important proteins cannot connect to the cell surface and protect the cell from substances in the blood called complement. As a result, red blood cells break down too early. The red cells leak hemoglobin into the blood, which can pass into the urine. This can happen at any time, but is more likely to occur during the night or early morning.
The disease can affect people of any age. It may lead to aplastic anemia, myelodysplastic syndrome, or acute myelogenous leukemia.
Who is at highest risk?
Risk factors, except for prior aplastic anemia, are not known.
When to seek urgent medical care?
Call your health care provider if you find blood in your urine, if symptoms worsen or do not improve with treatment or if new symptoms develop.
Diagnosis
- Red or brown urine signals the breakdown of red blood cells and that hemoglobin is being released into the body's circulation and eventually into the urine.
- Tests that may be done to diagnose this condition may include:
- Complete blood count (CBC)
- Coombs' test
- Flow cytometry to measure certain proteins
- Ham's (acid hemolysin) test
- Serum hemoglobin and haptoglobin
- Sucrose hemolysis test
- Urinalysis
- Urine hemosiderin
Treatment options
- Steroids or other drugs that suppress the immune system may help slow the break down of red blood cells.
- Blood transfusions may be needed.
- Supplemental iron and folic acid are provided.
- Blood thinners may also be needed to prevent clot formation.
- Soliris (eculizumab) is a drug used to treat PNH. It blocks the breakdown of red blood cells.
- Bone marrow transplantation can cure this disease.
- All patients with PNH should receive vaccinations against certain types of bacteria to prevent infection. Ask your doctor which ones are right for you.
Where to find medical care for Paroxysmal nocturnal hemoglobinuria?
Directions to Hospitals Treating Paroxysmal nocturnal hemoglobinuria
Prevention
There is no known way to prevent this disorder.
What to expect (Outlook/Prognosis)?
- The outcome varies. Most people survive greater than 10 years after their diagnosis. Death can result from complications such as blood clot formation (thrombosis) or bleeding.
- In rare cases, the abnormal cells may decrease over time.
Possible complications
- Acute myelogenous leukemia
- Aplastic anemia
- Blood clots
- Death