Solving a Mystery . . . 8 Years Later
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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| Format: | Book |
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SAGE Publishing,
2018-01-01T00:00:00Z.
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| 100 | 1 | 0 | |a Hayan Jouni MD |e author |
| 700 | 1 | 0 | |a Ronald S. Kuzo MD |e author |
| 700 | 1 | 0 | |a Nandan S. Anavekar MBBCh |e author |
| 245 | 0 | 0 | |a Solving a Mystery . . . 8 Years Later |
| 260 | |b SAGE Publishing, |c 2018-01-01T00:00:00Z. | ||
| 500 | |a 2324-7096 | ||
| 500 | |a 10.1177/2324709617752962 | ||
| 520 | |a 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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| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Journal of Investigative Medicine High Impact Case Reports, Vol 6 (2018) | |
| 787 | 0 | |n https://doi.org/10.1177/2324709617752962 | |
| 787 | 0 | |n https://doaj.org/toc/2324-7096 | |
| 856 | 4 | 1 | |u https://doaj.org/article/f210b0a1c3d64267be6ffe160d9c35c5 |z Connect to this object online. |