Asaeda Masahiro, Kurosaki Masamichi, Kambe Atsushi, Takenobu Atsumi, Horie Yasushi, Yamane Yukou, Murakami Yoshio, Watanabe Takashi
Division of Neurosurgery, Institute of Neurological Sciences, Faculty of Medicine, Tottori University, 36-1 Nishi-cho, Yonago-shi, Tottori 683-8504, Japan.
No To Shinkei. 2004 Mar;56(3):243-6.
We report an 80-year-old woman who was admitted to our hospital with symptoms due to diabetes insipidus. Magnetic resonance (MR) imaging demonstrated a sellar/suprasellar cystic lesion with marginal enhancement and the thick pituitary stalk. The MR imaging depicted edema spreading along the optic tract on fluid-attenuated inversion recovery (FLAIR) images. Upon neurological examination at the time of admission, there were no abnormal findings affecting the field of vision or visual acuity. In endocrinological examination, the basal plasma values of pituitary hormones were within normal range except for that of prolactin, which was 47.9 ng/ml. The preoperative diagnosis was craniopharyngioma, and the intrasellar mass was partially removed by the endoscopic transnasal transsphenoidal approach. Postoperative histopathological examination revealed Rathke's cleft cyst associated with squamous metaplasia. Lymphocytic infiltration was also confirmed in both the anterior and posterior pituitary lobe. The postoperative course was satisfactory. Edema spreading along the optic tract was reported as a characteristic MR imaging finding for diagnosis of craniopharyngiomas or optic nerve glioma. However, it is suggested that edema of the optic pathway seems to be caused not only by craniopharyngioma but also other suprasellar lesions. It was a rare case of secondary lymphocytic hypophysitis caused by Rathke's cleft with edema along the optic tract.
我们报告了一名80岁女性,因尿崩症症状入院。磁共振成像显示鞍区/鞍上囊性病变,边缘强化,垂体柄增厚。磁共振成像在液体衰减反转恢复(FLAIR)图像上显示水肿沿视束扩散。入院时神经检查未发现影响视野或视力的异常。在内分泌检查中,除催乳素为47.9 ng/ml外,垂体激素的基础血浆值均在正常范围内。术前诊断为颅咽管瘤,经鼻内镜经蝶窦入路部分切除鞍内肿物。术后组织病理学检查显示拉克氏囊肿伴鳞状化生。垂体前叶和后叶均证实有淋巴细胞浸润。术后病程顺利。水肿沿视束扩散是颅咽管瘤或视神经胶质瘤诊断的特征性磁共振成像表现。然而,提示视路水肿似乎不仅由颅咽管瘤引起,也可由其他鞍上病变引起。这是一例由拉克氏囊肿伴视束水肿引起的继发性淋巴细胞性垂体炎罕见病例。