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Optic neuritis in a child with Rathke cleft cyst Namie Kobayashi 1,2 , Kentaro Kobayashi 2 , Takatsugu Onoda 2 , Yi-Ning Chen 2 , Hidetoshi Ikeda 3 , Emiko Adachi-Usami 4 1Dept of Ophthalmol, Southern Tohoku Gen Hosp 2Southern Tohoku Eye Clin 3Neurosurgery Res Inst for Pituitary Dis, Southern Tohoku Gen Hosp 4Chiba Univ pp.1189-1195
Published Date 2014/8/15
DOI https://doi.org/10.11477/mf.1410105350
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Abstract. Purpose:To report a child with recurrent unilateral optic neuritis secondary to Rathke cleft cyst. Case:A 15-year-old boy presented with impaired vision in the right eye. He had had migaine and decreased vision to 0.3 in the right eye 4 years before. Peroal prednisolone was followed by recovery of vision. Findings:Corrected visual acuity was counting fingers right and 1.2 left. Funduscopy showed normal findings. Fluorescein angiography showed hyperfluorescence towards the late phase. Peroral prednisolone was followed by improvement of vision one month later. Right visual acuity gradually decreased to 0.1 during the following 5 months associated with migraine, visual field defect, and attacks of fainting. Fourteen months after his initial visit, computed tomography showed Rathke cleft cyst adjacent to the pituitary gland. Excision of the cyst was followed by improvement of vision to 1.2 and of visual field. Conclusion:This case illustrates that Rathke cleft cyst may induce symptoms simulating optic neuritis in childhood.


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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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