Multi-System Langerhans Cell Histiocytosis as a Mimic of IgG4-Related Disease: A Case Report and Literature Review

Langerhans cell histiocytosis (LCH) is a rare disease characterized by the clonal accumulation and/or proliferation of specific dendritic cells resembling normal epidermal Langerhans cells (LCs). Clinical manifestations are variable, depending on the affected tissues or organs, however, LCH with ele...

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Detalles Bibliográficos
Autores principales: Feng, Xiaohui, Zhang, Lu, Chen, Fuqiong, Yuan, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353717/
https://www.ncbi.nlm.nih.gov/pubmed/35937835
http://dx.doi.org/10.3389/fendo.2022.896227

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353717/
https://www.ncbi.nlm.nih.gov/pubmed/35937835
http://dx.doi.org/10.3389/fendo.2022.896227

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