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Ependymoma of the Sella Turcica and Suprasellar Region Kohei HASHINO 1 , Taku SATO 1 , Yugo KISHIDA 1,2 , Yosuke KUROMI 1 , Yuichiro KIKO 3 , Masayuki YAMADA 1 , Masao TAMBARA 1 , Jun SAKUMA 1 , Kiyoshi SAITO 1 1Department of Neurosurgery, Fukushima Medical University 2Department of Neurosurgery, Japanese Red Cross Nagoya Daini Hospital 3Department of Diagnostic Pathology, Fukushima Medical University Keyword: ependymoma , suprasellar , sella turcica , transsphenoidal approach pp.185-191
Published Date 2021/1/10
DOI https://doi.org/10.11477/mf.1436204374
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 An ependymoma of the sella turcica and the suprasellar region has been described by only 10 reports in the available literature. We describe similar pathology in a 70-year-old woman who presented with dementia and visual disturbance. Magnetic resonance imaging with gadolinium revealed a mixed contrast-enhanced lesion(maximum diameter 3.5 cm)in the sella turcica and suprasellar area associated with a noncommunicating hydrocephalus. The patient was preoperatively presumptively diagnosed with a craniopharyngioma. The lesion was adherent to the hypothalamus, and the third ventricular floor was completely resected via an endoscopic endonasal transsphenoidal approach. Histopathological findings confirmed an ependymoma. Although her visual disturbance improved, the patient developed postoperative panhypopituitarism. She has had no recurrence for 7 years postoperatively. An ependymoma of the sella turcica and the suprasellar region is extremely rare; establishing the preoperative diagnosis is challenging in such patients. Maximum tumor resection and long-term follow-up are essential for good prognosis.


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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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