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Langerhans Cell Histiocytosis

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Pediatric Head and Neck Tumors

Abstract

Langerhans cell histiocytosis is characterized by the clonal proliferation of histiocytes, a type of white blood cell, in various organs of the body. There is a large range of presentations, from isolated lesions, most often of bone, to widespread, multisystem disease. Disease that appears to be isolated may be more widespread either at diagnosis or in the future, so broad workup and vigilant surveillance is required. Patients with involvement of only one organ system can often be cured with surgical resection or curettage alone, whereas patients with involvement of high-risk bony sites, risk organs, or widespread disease require chemotherapy and have variable outcomes.

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Correspondence to Carlos Rodriguez-Galindo MD .

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Green, A., Rodriguez-Galindo, C. (2014). Langerhans Cell Histiocytosis. In: Rahbar, R., Rodriguez-Galindo, C., Meara, J., Smith, E., Perez-Atayde, A. (eds) Pediatric Head and Neck Tumors. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-8755-5_26

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  • DOI: https://doi.org/10.1007/978-1-4614-8755-5_26

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