Histiocytosis

Histiocytosis is a general name for a group of syndromes that involve an abnormal increase in the number of immune cells known as histiocytes. The disease can affect anyone from infants to older adults.

Types of Histiocytosis[edit | edit source]

There are several types of histiocytosis, including:

Langerhans cell histiocytosis (LCH): This is the most common type of histiocytosis. LCH can damage skin, bones, and other parts of the body, or form tumors.

Non-Langerhans cell histiocytosis: This type includes a variety of conditions that cause histiocytes to build up in certain parts of the body, such as the skin, lymph nodes, and spleen.

Hemophagocytic lymphohistiocytosis (HLH): This is a severe form of histiocytosis that can affect many organs throughout the body.

Symptoms[edit | edit source]

The symptoms of histiocytosis can vary greatly depending on the type and severity of the condition. They may include:

Diagnosis[edit | edit source]

Histiocytosis is diagnosed through a combination of medical history, physical examination, and laboratory tests. These may include:

Treatment[edit | edit source]

Treatment for histiocytosis depends on the type and severity of the condition. It may include:

Prognosis[edit | edit source]

The prognosis for individuals with histiocytosis varies greatly. Some people may recover completely with treatment, while others may experience long-term complications or disability.

See Also[edit | edit source]

Histiocytosis Resources
Need Help Finding a Doctor? Need help finding a doctor or specialist anywhere in the world? Explore our world directory. WikiMD's DocFinder can assist you in locating millions of physicians.	Medical Knowledge Access the latest research - Most recent articles Ongoing trials.