| Literature DB >> 18584981 |
Cyril Mignot1, Isabelle Desguerre, Lydie Burglen, Lucie Hertz-Pannier, Florence Renaldo, Jean-François Gadisseux, Serge Gallet, Danielle Pham-Dinh, Odile Boespflug-Tanguy, Diana Rodriguez.
Abstract
We report a patient with infantile Alexander disease (AXD) due to the recurrent p.Arg79Cys GFAP mutation. In addition to typical AXD abnormalities, magnetic resonance imaging demonstrated a tumor-like lesion of the optic chiasm suggestive of a glioma. A transient papilloedema appeared during the follow-up and the lesion partially regressed despite a worsening of white matter involvement. Rare radiological and pathological tumor-like lesions have already been reported in AXD patients. This patient confirms that enlargement of the optic chiasm is a rare feature of AXD, possibly linked to abnormal astrocytic proliferation.Entities:
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Year: 2008 PMID: 18584981 DOI: 10.1016/j.braindev.2008.05.005
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961