Histiocytosis
 
histio_kid.jpg (119977 bytes) Histiocytosis is a rare blood disease that is caused by an excess of white blood cells called histiocytes. The histiocytes cluster together and can attack the skin, bones, lungs, liver, spleen, gums, ears, eyes and/or the central nervous system. The disease can range from limited involvement that spontaneously regresses to progressive multi-organ involvement that can be chronic and debilitating. In some cases the disease can be life threatening.

In some ways, histiocytosis is similar to cancer and has historically been treated by oncologists with chemotherapy and/or radiation. Unlike cancer, histiocytosis sometimes goes into remission without treatment. The vast majority of people diagnosed with histiocytosis are children under the age of ten, but it is also found in adults of all ages.

Histiocytosis affects roughly 1 in 200,000 children born each year in the United States. Histiocytosis is so rare that there is little research into its cause and treatment and is often referred to as an "orphan disease", meaning it strikes too few people to generate government-supported research.

For more information on Histiocytosis:  www.histio.org

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