Erdheim-Chester disease with chorioretinal and orbital involvement: a case report
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info:eu-repo/semantics/closedAccessTarih
2024Yazar
Cabuk, Kubra SerefogluTellioglu, Adem
Karabulut, Gamze Ozturk
Nacaroglu, Senay Asik
Fazil, Korhan
Elverdi, Tugrul
Taskapili, Muhittin
Karslioglu, Safak
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Cabuk, K. S., Tellioglu, A., Karabulut, G. O., Nacaroglu, S. A., Fazil, K., Elverdi, T., ... & Karslioglu, S. (2023). Erdheim-Chester disease with chorioretinal and orbital involvement: a case report. Arquivos Brasileiros de Oftalmologia.Özet
A 42-year-old woman presented with bilateral proptosis, chemosis, leg pain, and vision loss. Orbital, chorioretinal, and multi-organ involvement of Erdheim- Chester disease, a rare non-Langerhans histiocytosis, with a negative BRAF mutation was diagnosed based on clinical, radiological, and pathological findings. Interferon-alpha-2a (IFN alpha-2a) was started, and her clinical condition improved. However, 4 months later, she had vision loss with a history of IFN alpha 2a cessation. The same therapy was administered, and her clinical condition improved. The Erdheim-Chester disease is a rare chronic histiocytic proliferative disease that requires a multidisciplinary approach and can be fatal if left untreated because of multisystemic involvements.
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ARQUIVOS BRASILEIROS DE OFTALMOLOGIACilt
87Sayı
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