Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages
Université Paris-Saclay · Assistance Publique – Hôpitaux de Paris · +27 more institutions
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…
Citation impact
- FWCI
- 74.88
- Percentile
- 100%
- References
- 105
Authors
24- JEJean‐François EmileCorresponding
Université Paris-Saclay, Assistance Publique – Hôpitaux de Paris, Hôpital Ambroise-Paré
- OAOussama Abla
University of Toronto, Hospital for Sick Children, SickKids Foundation
- SFSylvie Fraitag
Hôpital Necker-Enfants Malades
- AHAnnaCarin Horne
Karolinska University Hospital, Karolinska Institutet
- JHJulien Haroche
Sorbonne Université, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital
Topics & keywords
- Histiocyte
- Histiocytosis
- Pathology
- Hemophagocytic lymphohistiocytosis
- Mucocutaneous zone
- Medicine
- Langerhans cell histiocytosis
- Erdheim–Chester disease
- Good health and well-being