Abstract
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multisystem involvement and insidious symptoms. In this article, we describe an interesting case of Erdheim-Chester disease that was eventually diagnosed 8 years after symptoms initially started.
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APA
Jouni, H., Kuzo, R. S., & Anavekar, N. S. (2018). Solving a mystery … 8 years later. Journal of Investigative Medicine High Impact Case Reports, 6. https://doi.org/10.1177/2324709617752962
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