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1例结节性硬化症合并松果体区肿瘤

[A case of tuberous sclerosis associated with a pineal region tumor].

作者信息

Kurimoto M, Ohara S, Nakagaki S, Aoki S, Mori M

出版信息

No Shinkei Geka. 1987 Feb;15(2):167-71.

PMID:3561682
Abstract

The authors report a rare case of tuberous sclerosis associated with pineal region mixed glioma. A 38-year-old woman with tuberous sclerosis, who had a past history of left nephrectomy and tumorectomy of the right kidney for bilateral renal angiomyolipomas, was admitted because of headache and ataxic gait. CT scan and cerebral angiography suggested a pineal region tumor. Suboccipital craniectomy and partial removal of the tumor was performed via infratentorial supracerebellar approach. Microscopic examination revealed mixed oligodendroglioma and astrocytoma. It is well known that tuberous sclerosis is occasionally associated with brain tumors. However, with few exceptions, these have been subependymal giant cell astrocytomas in the lateral ventricles. They seem to originate from subependymal nodules of hamartomatous nature. As far as we are aware, association of pineal region tumor with tuberous sclerosis as in this case has not been reported.

摘要

作者报告了一例罕见的结节性硬化症合并松果体区混合性胶质瘤病例。一名38岁患有结节性硬化症的女性,既往因双侧肾血管平滑肌脂肪瘤接受过左肾切除术和右肾肿瘤切除术,因头痛和共济失调步态入院。CT扫描和脑血管造影提示松果体区肿瘤。通过枕下小脑上入路进行了枕下颅骨切除术和肿瘤部分切除术。显微镜检查显示为少突胶质细胞瘤和星形细胞瘤混合。众所周知,结节性硬化症偶尔会与脑肿瘤相关。然而,除少数例外,这些肿瘤均为侧脑室内的室管膜下巨细胞星形细胞瘤。它们似乎起源于错构瘤性质的室管膜下结节。据我们所知,像本例这样的松果体区肿瘤与结节性硬化症的关联尚未见报道。

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