Agranulocytosis is a low level of white blood cells. These blood cells are part of the immune system. They help fight infections.
Agranulocytosis may be: Acquired—Develops after medical treatment or specific drugs. May appear suddenly or develop over time.
Congenital—present at birth
Cyclic neutropenia—cycles up and down over a 21-day periodSevere congenital neutropenia
White Blood Cells
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Agranulocytosis is caused by destruction of white blood cells or by the failure of bone marrow to make enough white blood cells.
With congenital agranulocytosis, these problems are caused by a genetic defect.
With acquired agranulocytosis, these problems may be caused by: Infections by virus, bacteria, or parasiteUnderlying inflammatory conditionChemotherapyDrugs—used in medical treatment or recreational useAutoimmune disease—your immune systems attacks your own tissue such as white blood cellsDamage to bone marrow usually by chemicals, radiation, or cancersCertain toxinsPoor nutrition—particularly low protein intake
Factors that increase your chance of developing agranulocytosis include: Undergoing chemotherapy treatment for cancerTaking certain medications, including some antithyroid medication, antidepressants, antihistamines, and anticonvulsantsInfectionExposure to certain chemical toxins or radiationAutoimmune diseasesEnlargement of the spleenVitamin B-12 or folate deficiencyLeukemia
myelodysplastic syndromesAplastic anemia or other diseases of the bone marrowFamily history of certain genetic diseases
Symptoms of agranulocytosis may include:
Rapid onset of fever, chills,
jaundice, weakness, or
sore throatMouth soresBleeding gums
Symptoms of congenital agranulocytosis may include: Mild infections of skin, mouth, and nosePoor weight gain in children
Your doctor will ask about your symptoms and medical history. You will be asked about recent infections, medical treatments, and medications. A physical exam will be done.
Your bodily fluids and tissues may be tested. This can be done with: Blood testsBone marrow testUrine tests
Treatment will be based on the type and cause of agranulocytosis that you have. Options include the following:
Leukocytes are a type of white blood cell. These cells are collected from a donor and carefully screened. They are then delivered through an IV. These white blood cells may make up for the deficit caused by agranulocytosis.
Antiviral, antibiotic, and antifungal medication may be needed to: Treat an infection that could be causing agranulocytosisTreat an infection that resulted from agranulocytosisPrevent an infection in people at high risk—this may include people with cancer or immune disorders
Granulocyte colony-stimulating factor (G-CSF) or granulocyte-macrophage colony-stimulating factor (GM-CSF) encourages the body to make more white blood cells. This may help with certain types of agranulocytosis.
When possible, the toxin or drug that is causing the problems will be removed.
Your doctor will monitor you if you are taking medication or having medical treatment that could lead to agranulocytosis. You may be given white blood cell stimulating medications before having treatments. This may prevent agranulocytosis.
Boulton F, Cooper C, et al. Neutropenia and agranulocytosis in England and Wales: incidence and risk factors.
American Journal of Hepatology. 2003 Apr;72(4):248-54.
Last reviewed August 2013 by Michael Woods, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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