Suppr超能文献

急性小脑性共济失调作为伊默斯伦德-格里斯贝克综合征的首发表现。

Acute cerebellar ataxia as the first manifestation of Imerslund-Gräsbeck syndrome.

作者信息

Eslamiyeh Hosein

机构信息

1.Pediatric Neurology, Department of Pediatrics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

出版信息

Iran J Child Neurol. 2021 Fall;15(4):105-108. doi: 10.22037/ijcn.v15i4.27482.

Abstract

Imerslund-Gräsbeck syndrome is a rare condition caused by vitamin B12 deficiency and proteinuria. In this article, we reported the case of a 10-year-old girl with imbalance and urinary incontinence. The case had cerebellar ataxia as the primary manifestation. The disequilibrium had progressed gradually within three weeks and was consistent with the symptoms of cerebellar involvement and urinary incontinence. Brain and cervico-thoraco-lumbar magnetic resonance imaging were normal. The patient had elevated lactate dehydrogenase (LDH=4775), in addition to macrocytic anemia, on laboratory examinations; thus, the possibility of malignancy was raised. Then, bone marrow aspiration was performed, showing hypercellular marrow with megaloblastic changes. This finding proved megaloblastic anemia. Regarding the low prevalence of vitamin B12 deficiency in healthy individuals, extensive studies were performed to find out the cause. The serum level of vitamin B12 was found to be lower than the normal range. Although urinalysis revealed significant proteinuria, further nephrological investigations did not indicate any abnormalities. No evidence of serious problems was observed in the gastrointestinal tract study, and metabolic studies were normal. Finally, based on the obtained data, Imerslund-Gräsbeck syndrome was recognized. Patient was treated by vitamin B12 injection, leading to improved balance, and in one-month follow-up, she was able to walk independently, and the cerebellar symptoms had greatly disappeared; however, proteinuria persisted.

摘要

艾默斯伦德 - 格雷斯贝克综合征是一种由维生素B12缺乏和蛋白尿引起的罕见病症。在本文中,我们报告了一名10岁女孩出现平衡失调和尿失禁的病例。该病例以小脑共济失调为主要表现。失衡在三周内逐渐进展,与小脑受累症状及尿失禁相符。脑及颈胸腰段磁共振成像均正常。实验室检查显示,除巨幼细胞贫血外,患者乳酸脱氢酶升高(LDH = 4775),因此引发了恶性肿瘤的可能性。随后进行骨髓穿刺,结果显示骨髓细胞增多并有巨幼细胞改变。这一发现证实为巨幼细胞贫血。鉴于健康个体中维生素B12缺乏的患病率较低,我们进行了广泛研究以找出病因。发现血清维生素B12水平低于正常范围。虽然尿液分析显示有明显蛋白尿,但进一步的肾脏检查未发现任何异常。胃肠道检查未发现严重问题的迹象,代谢研究也正常。最后,根据所获数据,确诊为艾默斯伦德 - 格雷斯贝克综合征。患者接受维生素B12注射治疗后,平衡能力有所改善,在一个月的随访中,她能够独立行走,小脑症状已大为消失;然而,蛋白尿仍然存在。

相似文献

引用本文的文献

本文引用的文献

5

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验