The clinical manifestations of Langerhans cell histiocytosis in the central
nervous system include not only the classical involvement of the hypothala
mus-hypophyseal axis, but also of other anatomic locations, with the corres
ponding variability of symptoms.
We report here two patients with meningeal lesions. In both patients, the o
nset of the disease was systemic, and neurological symptoms developed some
years later. Imaging studies, particularly magnetic resonance, are very sen
sitive tools for the diagnosis and follow-up of these lesions.
The natural history of this disease is still poorly understood. In this pap
er we related the clinical manifestations to the morphological changes obse
rved in imaging studies.