Abstract
The histiocytoses are a group of disorders characterized by accumulation of variable number of monocytes, macrophages, and dendritic cells in affected tissues of children and adults. Many different subtypes have been described with a wide range of clinical features and histopathological changes.
Langerhans cell histiocytoses include spectrum of clinical manifestation ranging from self-healing lesions to life-threatening disseminated disease. Juvenile xanthogranuloma is the most common type of non-Langerhans cells histiocytoses, and some other subtypes may show overlapping features. Necrobiotic xanthogranuloma, Rosai-Dorfman disease, Erdheim-Chester disease, and multicentric reticulohistiocytosis are characterized by systemic involvement. Infiltrating cells of malignant histiocytoses show cancerous changes. The diagnosis of histiocytoses is based on clinical findings in combination with histopathological analysis identifying tissue infiltration by histiocytes with ultrastructural and immunophenotypic characteristics of cells. Various different chemotherapeutic agents, lasers, cryotherapy, and radiofrequency ablation have shown variable success in the treatment of histiocytoses.
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Kothiwala, S.K., Kumar, P., Mandal, R.K. (2019). Histiocytoses. In: Smoller, B., Bagherani, N. (eds) Atlas of Dermatology, Dermatopathology and Venereology . Springer, Cham. https://doi.org/10.1007/978-3-319-45134-3_84-2
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DOI: https://doi.org/10.1007/978-3-319-45134-3_84-2
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Latest
Histiocytoses- Published:
- 06 July 2019
DOI: https://doi.org/10.1007/978-3-319-45134-3_84-2
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Histiocytoses- Published:
- 16 October 2018
DOI: https://doi.org/10.1007/978-3-319-45134-3_84-1