Literature DB >> 7447764

Demyelinative chiamal lesions.

R H Spector, J S Glaser, N J Schatz.   

Abstract

To clarify the clinical syndrome of demyelinative chiasmal involvement, six case histories were analyzed and the literature was reviewed. This entitity is characterized by especial predilection for women in the third to fifth decades; visual deficites of a chiasmal pattern that may be modest to marked, with a generallly good prognosis for functional recovery; and other signs and symptoms, not necessarily severe, of scattered lesions of the neuraxis. Neuroradiological studies, especially laminography of the sellar area and computerized tomography, must be employed to rule out a suprasellar mass lesion. The efficacy of systemic corticosteroid therapy is moot, but it seems reasonable to use such agents during acute stages, especially where vision is severely reduced on both sides.

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Mesh:

Year:  1980        PMID: 7447764     DOI: 10.1001/archneur.1980.00500610037005

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  3 in total

1.  [Incomplete, incongruent homonymous hemianopsia toward the right].

Authors:  K H Eibl; A S Neubauer; A Kampik; M W Ulbig
Journal:  Ophthalmologe       Date:  2004-03       Impact factor: 1.059

2.  The diagnostic challenge of bilateral vision loss: a case of chiasmal optic neuritis.

Authors:  Selma Topaloglu; Ayhan Koksal; Nilüfer Kale Icen; Belgin Mutluay; Sevim Baybas
Journal:  Neurol Sci       Date:  2014-05-09       Impact factor: 3.307

3.  Chiasmal apoplexy: haemorrhage from a cavernous malformation in the optic chiasm.

Authors:  L Regli; N de Tribolet; F Regli; J Bogousslavsky
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-09       Impact factor: 10.154

  3 in total

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