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  3. Langerhans cell histiocytosis of the head and neck in the pediatric population in a tertiary center: Clinical presentation, classification and treatment.

Langerhans cell histiocytosis of the head and neck in the pediatric population in a tertiary center: Clinical presentation, classification and treatment.

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Autores de IIS La Fe

Participantes ajenos a IIS La Fe

  • De Luca Sologaistoa A

Grupos

Abstract

Langerhans cell histiocytosis (LCH) is a rare disease of unknown etiology with a heterogeneous and unspecific clinical presentation. Any organ or system may be involved but the most frequent is the skeleton. The diagnostic gold standard is done through histopathology combined with immunohistochemistry in the correct clinical setting. Treatment is still controversial. The objective of this study is to present a series of pediatric patients in order to contribute to the diagnosis and treatment of LCH.

Copyright © 2022 Elsevier B.V. All rights reserved.

Datos de la publicación

ISSN/ISSNe:
0165-5876, 1872-8464

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY  ELSEVIER IRELAND LTD

Tipo:
Article
Páginas:
111073-111073
PubMed:
35220158
Factor de Impacto:
0,579 SCImago ℠
Cuartil:
Q2 SCImago ℠

Citas Recibidas en Web of Science: 8

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Keywords

  • Birbeck granules, Head and neck, Langerhans cell histiocytosis, Langerin, Pediatric, Temporal bone

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