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A case of multisystem Langerhans cell histiocytosis presenting as central diabetes insipidus
Langerhans cell histiocytosis (LCH) is a rare malignancy most commonly characterized by histiocytic infiltration of bone. LCH lesions in the skull place the adjacent central nervous system (CNS) at risk for involvement, which can manifest as central diabetes insipidus (CDI) when there is infiltratio...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Taylor & Francis
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968576/ https://www.ncbi.nlm.nih.gov/pubmed/32002162 http://dx.doi.org/10.1080/20009666.2019.1698231 |