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In medicine, histiocytosis is an excessive number of histiocytes[1] (tissue macrophages), and the term is also often used to refer to a group of rare diseases which share this sign as a characteristic. Occasionally and confusingly, the term histiocytosis is sometimes used to refer to individual diseases.
| Histiocytosis | |
|---|---|
| Specialty | Hematology  |
According to the Histiocytosis Association, 1 in 200,000 children in the United States are born with histiocytosis each year.[2] HAA also states that most of the people diagnosed with histiocytosis are children under the age of 10, although the disease can afflict adults. The disease usually occurs from birth to age 15.[3]
Histiocytosis (and malignant histiocytosis) are both important in veterinary as well as human pathology.
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Histiocytosis is a rare disease, thus its diagnosis may be challenging. A variety of tests may be used, including:[5]
- Imaging
- CT scans of various organs such as lung, heart and kidneys.
- MRI of the brain, pituitary gland, heart, among other organs.
- Skeletal survey is useful in children
- Ultrasound of liver and spleen
- Blood tests: measure cell counts and inflammation
- Breathing tests
- Tissue biopsy and molecular testing to detect mutations
There are competing systems for classifying histiocytoses. According to the 1999 classification proposed by the World Health Organization, they can be divided into three categories.[6][7] However, the classifications in ICD10 and MeSH are slightly different, as shown below:
| Name | WHO | ICD10 | MeSH |
|---|---|---|---|
| Langerhans cell histiocytosis (LCH) | I | D76.0 | Langerhans-cell histiocytosis |
| Juvenile xanthogranuloma (JXG) | II | D76.3 | non-Langerhans-cell histiocytosis |
| Hemophagocytic lymphohistiocytosis (HLH) | II | D76.1 | non-Langerhans-cell histiocytosis |
| Niemann–Pick disease | II | E75.2 | non-Langerhans-cell histiocytosis |
| Sea-blue histiocytosis | II | – | non-Langerhans-cell histiocytosis |
| Acute monocytic leukemia | III | C93.0 | malignant histiocytic disorders |
| Malignant histiocytosis | III | C96.1 | malignant histiocytic disorders |
| Erdheim–Chester disease | II | C96.1 | malignant histiocytic disorders |
Alternatively, histiocytoses may be divided into the following groups:[8]: 714–724
Lymphohistiocytosis is a similar immune system disease characterized by the inappropriate activation of natural killer cells, CD8+ cytotoxic T-cells, and macrophages, involving principally the liver, spleen and central nervous system and associated with severe lymphoid atrophy.[9][10]
Various treatments exist for histiocytosis. The one selected depends on the location of the disease and the patient history. The modalities used may include:[11]
- Chemotherapy
- Cladribine (also known as 2CDA or Leustatin)
- Etoposide
- Methotrexate
- 6-mercaptopurine
- Vinblastine
- Surgery
- Radiation therapy
Patients and families can gain support and educational materials from the Histiocytosis Association.[citation needed]
The Histiocyte Society, a nonprofit organization, is a group of more than 200 physicians and scientists from around the world committed to improving the lives of patients with histiocytic disorders by conducting clinical and laboratory research into the causes and treatment of this disease. The Society has instituted several clinical trials and treatment plans.[12][13]
The North American Consortium for Histiocytosis (NACHO) is a group of institutions that collaborate on scientific and clinical research for histiocytic diseases. Established in 2014 by 12 institutions, it was funded through a consortium grant from the St. Baldrick's Foundation.[14]
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