放射学与病理学的相关性:罗赛-多夫曼病

IF 1.3 Q4 NEUROIMAGING Neuroradiology Journal Pub Date : 2024-11-20 DOI:10.1177/19714009241303077
John C Benson, Alex B Pais, Ian T Mark, William O Tobin, John J Chen, Frederic B Meyer, Christopher H Hunt, Caterina Giannini
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引用次数: 0

摘要

罗赛-多夫曼病(Rosai-Dorfman Disease,RDD)又称窦性组织细胞增生症伴巨块淋巴结病,是一种罕见的非朗格汉斯细胞组织细胞肿瘤。虽然该病在青壮年中通常表现为大量无痛性淋巴结病,但有些患者的中枢神经系统也会受累。中枢神经系统病变可导致头痛、神经功能缺损,甚至神经功能障碍。中枢神经系统 RDD 的影像学表现通常与脑膜瘤相似:以硬脑膜为基础的圆形病变,通常有硬脑膜尾部。不过,也有一些影像学线索可以帮助放射科医生识别 RDD,甚至在组织病理学确诊之前。这篇中枢神经系统 RDD 患者的放射病理报告强调了中枢神经系统 RDD 最相关的临床、影像和病理特征,并讨论了神经放射科医生需要了解的疾病相关知识。
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Radiology-pathology correlation: Rosai-Dorfman disease.

Rosai-Dorfman Disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytic neoplasm. Although the disease classically presents as massive painless lymphadenopathy in young adults, RDD can also involve the central nervous system in some patients. CNS lesions, can cause headaches, neurologic deficits, and even neurologic deficits. The imaging appearance of CNS RDD typically mimics that of meningiomas: well-circumscribed dural-based lesions that often have dural tails. However, some imaging clues also exist that might help a radiologist recognize RDD, even before histopathologic confirmation. This radiology-pathology report of a patient with CNS RDD highlights the most pertinent clinical, imaging, and pathologic features of CNS RDD, and discusses what the neuroradiologist needs to know about the disease.

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来源期刊
Neuroradiology Journal
Neuroradiology Journal NEUROIMAGING-
CiteScore
2.50
自引率
0.00%
发文量
101
期刊介绍: NRJ - The Neuroradiology Journal (formerly Rivista di Neuroradiologia) is the official journal of the Italian Association of Neuroradiology and of the several Scientific Societies from all over the world. Founded in 1988 as Rivista di Neuroradiologia, of June 2006 evolved in NRJ - The Neuroradiology Journal. It is published bimonthly.
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