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Adult-onset Langerhans cell histiocytosis changing CNS lesion from pituitary to suprasellar extension
SUMMARY: Langerhans cell histiocytosis (LCH) is a rare disease characterized by the proliferation of abnormal Langerhans cells in various tissues and organs, including bone, skin, the lungs, and the pituitary gland. Hypothalamic–pituitary lesions in LCH often cause central diabetes insipidus (CDI),...
Autores principales: | Kadowaki, Yuji, Nishiyama, Mitsuru, Nakamura, Makoto, Morisaka, Hiroyuki, Fujimoto, Shimpei, Terada, Yoshio, Kojima, Kensuke |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175615/ https://www.ncbi.nlm.nih.gov/pubmed/35642690 http://dx.doi.org/10.1530/EDM-22-0232 |
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