SUN-271 Langerhans Cell Histiocytosis: A Difficult Diagnosis in Cranial Diabetes Insipidus

Background Langerhans cell histiocytosis (LCH) is a myeloid neoplastic disorder that is rare in adults, with a reported incidence of 1-2 cases per million per year. Cranial diabetes insipidus (CDI) is the most common and often the first endocrine manifestation of LCH, when histiocytes infiltrate the...

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Veröffentlicht in:J Endocr Soc
Hauptverfasser: Ng, Ivy Hoi Yee, Cheung, Elaine Yun Ning, Kam, Grace Yee Wai
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2020
Schlagworte:
Neuroendocrinology and Pituitary
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7209532/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.644
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