Vol 59, No 1 (2025)
Response to Letter to the Editors
Published online: 2025-01-17
From rarity to reality: Poland’s first case of neurological Erdheim-Chester Disease with cerebellar manifestations
Abstract
Not available
References
- Finsterer J, Mehri S. Erdheim-Chester disease is often complicated by neurological disorders. Neurol Neurochir Pol. 2024 [Epub ahead of print].
- 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; 58(5): 538–541.
- 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).
- Goyal G, Heaney ML, Collin M, et al. Erdheim-Chester disease: consensus recommendations for evaluation, diagnosis, and treatment in the molecular era. Blood. 2020; 135(22): 1929–1945.
- 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.
- Pegoraro F, Papo M, Cohen-Aubart F, et al. Long-term outcome and prognosis of mixed histiocytosis (Erdheim-Chester disease and Langerhans Cell Histiocytosis). EClinicalMedicine. 2024; 73: 102658.
