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),...

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Detalles Bibliográficos
Autores principales: Kadowaki, Yuji, Nishiyama, Mitsuru, Nakamura, Makoto, Morisaka, Hiroyuki, Fujimoto, Shimpei, Terada, Yoshio, Kojima, Kensuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
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

Internet

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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