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[间脑综合征——三例报告]

[Diencephalic syndrome--report of three cases].

作者信息

Nishimoto A, Namba S, Yagyu Y

出版信息

No Shinkei Geka. 1984 Feb;12(2):211-9.

PMID:6717744
Abstract

Three cases of diencephalic syndrome, associated with brain tumors, are reported in this paper. Case 1. A 2-2/12-year old boy was initially admitted to our hospital because of failure to thrive which began at the age of three months. Physical examination revealed emaciation (weight, 7.8 kg), irritability and pallor without anemia. Horizontal nystagmus was seen. Laboratory studies were normal except for abnormally high plasma growth hormone (p-GH) which was incompletely suppressed by hyperglycemia (induced by glucose) and was not elevated by hypoglycemia (induced by insulin). A low grade astrocytoma of the optic nerve compression the hypothalamus was partially removed. After the operation followed by irradiation, p-GH returned to normal both in its basal level and in its reaction to insulin loading, then his gain of weight was accelerated. He was readmitted, however, at the age of 6 8/12 years with headache and vomiting. Since subtotal removal of the recurrent tumor and irradiation, preoperative symptoms have disappeared up to the present (7 9/12 years old). Case 2. A 3-9/12-year old girl was initially admitted because of failure to thrive since the age of 2 years. Examination on admission revealed emaciation (10.5 kg), irritability and right hemiparesis. Laboratory studies were normal except for high serum cholesterol (290 mg/dl). (p-HG was not measured) The patient had been well after the subtotal removal of the hypothalamic astrocytoma except occasional headache until the age of 6 years. She was readmitted at the age of 9 years with progressive emaciation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文报告了3例与脑肿瘤相关的间脑综合征病例。病例1:一名2岁2个月大的男孩因3个月大时开始出现发育不良而首次入院。体格检查发现消瘦(体重7.8千克)、易激惹和面色苍白但无贫血。可见水平性眼球震颤。实验室检查除血浆生长激素(p-GH)异常升高外均正常,该激素未被高血糖(由葡萄糖诱导)完全抑制,且未因低血糖(由胰岛素诱导)而升高。视神经低级星形细胞瘤压迫下丘脑,部分切除肿瘤。术后放疗后,p-GH的基础水平及其对胰岛素负荷的反应均恢复正常,随后其体重增加加速。然而,他在6岁8个月时因头痛和呕吐再次入院。自复发性肿瘤次全切除及放疗后,术前症状至今(7岁9个月)已消失。病例2:一名3岁9个月大的女孩因2岁起发育不良首次入院。入院检查发现消瘦(10.5千克)、易激惹和右侧偏瘫。实验室检查除高血清胆固醇(290毫克/分升)外均正常。(未检测p-HG)下丘脑星形细胞瘤次全切除后,患者情况良好,只是偶尔头痛,直到6岁。她在9岁时因进行性消瘦再次入院。(摘要截于250字)

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