Cryptococcosis
Cryptococcosis is an acute or chronic, localized or disseminated infection by few species of Cryptococcus (most often Cryptococcus neoformans or Cryptococcus gattii).
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Cryptococcosis is believed to be acquired by inhalation of the infectious propagule from the environment. In humans, C. neoformans causes three types of infections: Sites of involvement include the lungs, central nervous system and meninges, skin, and visceral organs.
- Wound or cutaneous cryptococcosis
- Pulmonary cryptococcosis
- Cryptococcal meningitis.
Risk factors[edit | edit source]
Cryptococcosis is a defining opportunistic infection for AIDS, and is the second-most-common AIDS-defining illness in Africa. Other conditions that pose an increased risk include certain lymphomas (e.g., Hodgkin's lymphoma), sarcoidosis, liver cirrhosis, and patients on long-term corticosteroid therapy. The prevalence of cryptococcosis has been increasing over the past 20 years for many reasons, including the increase in incidence of AIDS and the expanded use of immunosuppressive drugs.
Cryptococcosis can rarely occur in the non-immunosuppressed people, particularly with Cryptococcus gattii.
Additional images[edit | edit source]
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Prevention[edit | edit source]
Antifungal prophylaxis such as fluconazole and itraconazole reduces the risk of contracting cryptococcosis in those with low CD4 cell count and high risk of developing such disease in a setting of cryptococcal antigen screening tests are not available.
Treatment[edit | edit source]
Treatment options in persons without HIV-infection have not been well studied. Intravenous Amphotericin B combined with flucytosine by mouth is recommended for initial treatment (induction therapy).
The medication(s) listed below have been approved by the Food and Drug Administration (FDA) as orphan products for treatment of this condition.
Amphotericin B Liposomal (Brand name: AmBisome®) can be used in the treatment of disseminated cryptococcosis including
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NIH genetic and rare disease info[edit source]
Cryptococcosis is a rare disease.
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Contributors: Prab R. Tumpati, MD
