孤立的颅内模拟脑膜瘤的Rosai-Dorfman病1例报告。

Taehan Yongsang Uihakhoe chi Pub Date : 2022-05-01 Epub Date: 2022-05-25 DOI:10.3348/jksr.2021.0121
Minji Shin, Young Jin Heo, Donghyun Kim, Hae Woong Jeong, Jin Wook Baek, Ha Young Park
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引用次数: 0

摘要

罗赛-多尔夫曼病(Rosai-Dorfman Disease, RDD)是一种罕见的淋巴细胞增生性疾病,孤立性颅内RDD的发生极为罕见。颅内rdd多数表现为硬脑膜肿块,MRI呈均匀强化,术前难以与脑膜瘤鉴别,除非发现大量颈淋巴肿大。我们在此报告一例罕见的孤立性颅内RDD病例,患者为65岁男性。脑MRI显示一个明确的肿块样病变,包括右额叶凸出和轻微的扩散限制。然而,术前脑血管造影仅观察到轻微的腮红。虽然孤立性颅内RDD的病例很少见,但当在脑血管造影上发现伴有血管不足的硬脑膜肿块时,应考虑作为潜在的鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Isolated Intracranial Rosai-Dorfman Disease Mimicking Meningioma: A Case Report.

Isolated Intracranial Rosai-Dorfman Disease Mimicking Meningioma: A Case Report.

Rosai-Dorfman Disease (RDD) is a rare lymphoproliferative disease, and the occurrence of isolated intracranial RDD is extremely rare. Most cases of intracranial RDDs present as dural masses showing homogenous enhancement on MRI, which makes it difficult to differentiate these masses from meningiomas before surgery unless massive cervical lymphadenopathy is observed. We herein report a rare case of isolated intracranial RDD in a 65-year-old male. Brain MRI revealed a well-defined enhancing mass-like lesion involving the right frontal convexity and subtle diffusion restriction. However, only a subtle blush was observed on the preoperative cerebral angiogram. Although instances of isolated intracranial RDD are rare, it should be considered as a potential differential diagnosis when a dural mass with hypovascularity is visualized on the cerebral angiogram.

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