SUN-278 Isolated Hypothalamic Langerhans Cell Histiocytosis in an Adult Manifesting as Panhypopituitarism

Background: Langerhans Cell Histiocytosis (LCH) is a rare disease characterized by abnormal proliferation of bone marrow derived histiocytes. Although predominantly a childhood disease, LCH can occur at any age and has an incidence of one to two cases per million in adults. LCH can involve a single...

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Udgivet i:J Endocr Soc
Main Authors: Mikhael, Alexandra, Gautam, Nitesh, Buehler, Lauren Anne, Skugor, Mario
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2020
Fag:
Neuroendocrinology and Pituitary
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208031/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.133
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