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.

Detalles Bibliográficos
Autores principales: Jouni, Hayan, Kuzo, Ronald S., Anavekar, Nandan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804999/
https://www.ncbi.nlm.nih.gov/pubmed/29435464
http://dx.doi.org/10.1177/2324709617752962
Descripción
Sumario: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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