{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,6,1]],"date-time":"2025-06-01T18:22:16Z","timestamp":1748802136504},"reference-count":32,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["PED"],"published-print":{"date-parts":[[2015,5]]},"abstract":"<jats:p>Erdheim-Chester disease (ECD) is non-Langerhans histiocytosis that can affect multiple organ systems. It usually affects middle-aged patients, and only a few reports of ECD in children appear in the literature. Central nervous system involvement is a common feature that usually occurs as infiltration of the hypothalamus-pituitary axis, cerebellum, and\/or brainstem. Meningeal involvement occurs less commonly. In this article, the authors discuss a rare pediatric case of ECD presenting as an infiltrative mass of the trigeminal nerve and resembling the clinical and imaging features of a trigeminal schwannoma.<\/jats:p>","DOI":"10.3171\/2014.10.peds14441","type":"journal-article","created":{"date-parts":[[2015,2,27]],"date-time":"2015-02-27T14:57:58Z","timestamp":1425049078000},"page":"493-498","source":"Crossref","is-referenced-by-count":15,"title":["Erdheim-Chester disease mimicking an intracranial trigeminal schwannoma: case report"],"prefix":"10.3171","volume":"15","author":[{"given":"Maysam","family":"Alimohamadi","sequence":"first","affiliation":[{"name":"International Neuroscience Institute;"},{"name":"Iranian International Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christian","family":"Hartmann","sequence":"additional","affiliation":[{"name":"Department of Pathology, Medical School of 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