Vol 59, No 1 (2025)
Letter to the Editors
Published online: 2024-11-06
Erdheim-Chester disease is often complicated by neurological disorders
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Abstract
Not available
Keywords: Erdheim-Chester diseasehistiocytosisbrainneurological involvement
References
- Kaleta K, Możdżeń K, Murawska A, et al. From rarity to reality: Poland's first case of neurological Erdheim-Chester Disease with cerebellar manifestations. Neurol Neurochir Pol. 2024 [Epub ahead of print].
- Chrostowska P, Drozd-Sokołowska J, Miśkiewicz P. Erdheim‑Chester disease with orbital involvement and progressive impairment of vision. Pol Arch Intern Med. 2022; 132(4).
- Aubart FC, Poupel L, Saint-Charles F, et al. Profound systemic alteration of the immune phenotype and an immunoglobulin switch in Erdheim-Chester disease in 78 patients from a single center. Haematologica. 2022; 107(6): 1347–1357.
- Jezierska M, Stefanowicz J, Romanowicz G, et al. Langerhans cell histiocytosis in children - a disease with many faces. Recent advances in pathogenesis, diagnostic examinations and treatment. Postepy Dermatol Alergol. 2018; 35(1): 6–17.
- Manaka K, Makita N, Iiri T. Erdheim-Chester disease and pituitary involvement: a unique case and the literature. Endocr J. 2014; 61(2): 185–194.
- Aktan Suzgun M, Everest E, Kucukyurt S, et al. Erdheim-Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature. Neuropathology. 2024; 44(1): 59–67.
- Finsterer J. Double Subclavian Steal Syndrome As Initial Manifestation of Erdheim-Chester Disease: A Case Report. Cureus. 2023; 15(12): e50427.
