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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...
保存先:
| 出版年: | J Community Hosp Intern Med Perspect |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Taylor & Francis
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6968576/ https://ncbi.nlm.nih.gov/pubmed/32002162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/20009666.2019.1698231 |
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