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Introduction::Rosai-Dorfman disease (RDD) is an uncommon, benign, and idiopathic histiocytic proliferative disorder. Multiple intracranial RDD is extremely rare and treatment varies.Case presentation::A 9-year-old girl was admitted with 3-month history of blurred vision and facial paralysis, a 2-month history of recurrent giggle, and cognitive impairment. Computed tomography and magnetic resonance imaging scans revealed bilateral ventricular masses based on the dural membrane and the diameters of the masses were 9.1 cm and 9.2 cm, respectively. The lesions were completely removed with staging surgeries. Fifteen months after operation, blurred vision was still present but facial paralysis and giggle and cognitive impairment disappeared. Imaging examinations suggested that there were no new or recurring lesions.Conclusion::For multiple large intracranial masses, surgical treatment is necessary and staged surgery benefits perioperative safety. Active follow-up with magnetic resonance imaging is necessary.
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篇名 Staging surgery for intraventricular bilateral giant Rosai-Dorfman disease in children
来源期刊 儿科学研究(英文) 学科
关键词 Intraventricular Pediatric Rosai-Dorfman disease Sinus histiocytosis Staging surgery
年,卷(期) 2022,(1) 所属期刊栏目 Case Report
研究方向 页码范围 50-54
页数 5页 分类号
字数 语种 中文
DOI 10.1002/ped4.12306
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Intraventricular
Pediatric
Rosai-Dorfman disease
Sinus histiocytosis
Staging surgery
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
儿科学研究(英文)
季刊
2096-3726
10-1593/R
大16开
北京市西城区金融大街27号投资广场A座2101
2017
eng
出版文献量(篇)
198
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0
总被引数(次)
26
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