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神经垂体的颗粒细胞瘤伴视束水肿。

Granular cell tumor of the neurohypophysis with optic tract edema.

机构信息

Department of Radiology, Nihon University School of Medicine, 30-1 Kamicho Oyaguchi, Itabashi-ku, Tokyo, 173-8610, Japan,

出版信息

Jpn J Radiol. 2014 Mar;32(3):179-82. doi: 10.1007/s11604-013-0279-4. Epub 2014 Jan 11.

Abstract

Granular cell tumor of the neurohypophysis is a rare disease entity. To our knowledge, this is the first report concerning a granular cell tumor of the neurohypophysis associated with optic tract edema. A 55-year-old man underwent brain magnetic resonance imaging (MRI) for a medical check-up, and a suprasellar tumor was detected. Brain computed tomography (CT) demonstrated a well delineated, homogenous, slightly hyperdense suprasellar tumor. MRI detected a lobular tumor that was isointense on T1-weighted images, hypointense on T2-weighted images, and showed homogeneous enhancement after administration of a gadopentetate dimeglumine. T2-weighted images and fluid-attenuated inversion recovery (FLAIR) images demonstrated a hyperintense region in the optic tract. Subtotal tumor resection was performed, and histological examination confirmed the diagnosis of granular cell tumor. Postoperative MRI showed that the tumor volume was reduced and optic tract edema diminished compared with the preoperative findings. We also review the literature focusing on radiographic findings, and compare the effectiveness of MRI and CT for diagnosing granular cell tumor of the neurohypophysis.

摘要

垂体神经部颗粒细胞瘤是一种罕见的疾病。据我们所知,这是首例报道的垂体神经部颗粒细胞瘤伴有视束水肿。一位 55 岁男性因体检行颅脑磁共振成像(MRI)检查,发现鞍上区肿瘤。颅脑 CT 显示边界清楚、均匀的稍高密度鞍上区肿瘤。MRI 发现分叶状肿瘤,T1 加权像呈等信号,T2 加权像呈低信号,钆喷替酸葡甲胺增强后呈均匀强化。T2 加权像和液体衰减反转恢复(FLAIR)图像显示视束内高信号区域。行肿瘤次全切除术,组织学检查证实为颗粒细胞瘤。术后 MRI 显示与术前相比,肿瘤体积缩小,视束水肿减轻。我们还复习了文献,重点关注影像学表现,并比较了 MRI 和 CT 诊断垂体神经部颗粒细胞瘤的效果。

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