Langerhans' cell histiocytosis of the temporal lobe and pons
Makaleler > Tam Makale · 2004
Yazarlar: S Cagli, N Oktar, E Demirtas
British Journal of Neurosurgery, Uluslararası, Wos, 2004, cilt 18, ss 174-180
DOI: 10.1080/02688690410001681055
Özet
Intracerebral Langerhans' cell histiocytosis (LCH) is rare and tends to involve the hypothalamus. The authors report a rare case of LCH in the temporal lobe that subsequently was followed by a brainstem lesion. This appears to be the first case of temporal lobe and brainstem LCH that has been treated successfully and published. A 24-year-old man complained of cacosmia and nausea with a slight headache. He had a left temporal LCH, which was removed completely, but developed a brainstem lesion a year later. The pontine LCH was treated with radiosurgery. The follow-up period was 4 years without any neurological or radiological symptoms or signs. The 12 cases of solitary intracranial non-hypothalamic LCH reported previously are reviewed. Gamma knife radiosurgery effectively controlled the local growth of the pontine LCH without adverse effect.