Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages
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- 0.270 · how far apart the two teachers sit on this one work
- Validation status
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Abstract
The histiocytoses are rare disorders characterized by the accumulation of macrophage, dendritic cell, or monocyte-derived cells in various tissues and organs of children and adults. More than 100 different subtypes have been described, with a wide range of clinical manifestations, presentations, and histologies. Since the first classification in 1987, a number of new findings regarding the cellular origins, molecular pathology, and clinical features of histiocytic disorders have been identified. We propose herein a revision of the classification of histiocytoses based on histology, phenotype, molecular alterations, and clinical and imaging characteristics. This revised classification system consists of 5 groups of diseases: (1) Langerhans-related, (2) cutaneous and mucocutaneous, and (3) malignant histiocytoses as well as (4) Rosai-Dorfman disease and (5) hemophagocytic lymphohistiocytosis and macrophage activation syndrome. Herein, we provide guidelines and recommendations for diagnoses of these disorders.
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The record
- Venue
- Blood
- Topic
- Histiocytic Disorders and Treatments
- Field
- Medicine
- Canadian institutions
- SickKids FoundationHospital for Sick ChildrenUniversity of Toronto
- Funders
- National Cancer Institute
- Keywords
- HistiocyteHistiocytosisPathologyHemophagocytic lymphohistiocytosisMucocutaneous zoneMedicineLangerhans cell histiocytosisErdheim–Chester diseaseMacrophage activation syndromeRosai–Dorfman diseasePhenotypeBiologyDisease
- Has abstract in OpenAlex
- yes