Intracranial Rosai-Dorfman disease mimicking multiple meningiomas in a child: a case report and review of the literature

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• 作者：Yongji Tian ; Junmei Wang ; Jin zhao Ge ; Zhenyu Ma ; Ming Ge
• 关键词：Rosai ; Dorfman disease ; Central nervous system ; Child ; Meningiomas ; Sinus histiocytosis with massive lymphadenopathy
• 刊名：Child's Nervous System
• 出版年：2015
• 出版时间：February 2015
• 年：2015
• 卷：31
• 期：2
• 页码：317-323
• 全文大小：833 KB
• 参考文献：1. Foucar E, Rosai J, Dorfman R (1990) Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity. Semin Diagn Pathol 7:19-3
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• 刊物类别：Medicine
• 刊物主题：Medicine & Public Health
  Neurosurgery
  Neurosciences
  
• 出版者：Springer Berlin / Heidelberg
• ISSN：1433-0350

文摘

Objective Rosai-Dorfman disease (RDD) is a rare idiopathic, non-neoplastic histioproliferative disease. Central nervous system (CNS) manifestations are extremely rare. In this paper, we describe a 6-year-old boy with intracranial RDD mimicking multiple meningiomas both clinically and radiologically. We reviewed the literature to understand the clinical behaviour, clinicopathological features and treatment options. Methods A PubMed (US National Library of Medicine) search using the keywords ‘Rosai-Dorfman disease-and ‘central nervous system-was performed and citations were reviewed. Results Eighty-five cases of RDD involving the CNS have been reported until date, and only 7 cases involved children. Of the 85 cases, 16 cases mimicked multiple meningiomas. Our case is the first to involve multiple lesions in a child under 14?years old. Conclusion After reviewing the literature, we concluded that RDD should be considered as a differential diagnosis for lesions mimicking multiple meningiomas, especially in children. Resection of the intracranial lesion is the most effective treatment, and a definitive diagnosis should be based on histopathologic and immunocytochemical examinations.