American journal of medical genetics. Part A
From a Long-Standing Yellowish Plaque to a Diagnosis of a Rare Disorder: A Case of Erdheim-Chester Disease Treated With Vemurafenib.
Bugra Yilmaz, Gulsen Akoglu, Selim Sayin, Isinsu Kuzu, Hale Kivrak, Meltem Ayli
Published: 202610.1002/ajmga.70045
Abstract
Erdheim-Chester disease (ECD) is a rare, systemic, and potentially malignant non-Langerhans cell histiocytosis characterized by the infiltration of foamy histiocytes into multiple organ systems. The diagnosis of ECD is often complicated and time-cons…
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