Histiocytosis, often referred to as the “orphan disease,” is a rare blood disease that affects only about 1 in 200,000 children born each year in the US.
We have Arizona’s only histiocytosis team exclusively focused on the disease.
Our team benefits from working with the vast resources available to Phoenix Children’s and our Center for Cancer and Blood Disorders. This opportunity ensures our patients, and their loved ones, understand and benefit from the care and treatment journey.
A hallmark of histiocytosis is abnormal cell growth, but not necessarily cancerous growth. These cells are often found in the immune system and can manifest as Langerhans Cell Histiocytosis (LCH), Hemophagocytic Lymphohistiocytosis (HLH), Juvenile Xanthogranulomatosis (JXG) and Rosai-Dorfman Disease (RDD), among others.
