Benson John C, Pais Alex B, Mark Ian T, Tobin William O, Chen John J, Meyer Frederic B, Hunt Christopher H, Giannini Caterina
Department of Radiology, Mayo Clinic, Rochester, MN, USA.
Department of Neurologic Surgery, Mayo Clinic, Rochester, MN, USA.
Neuroradiol J. 2024 Nov 20:19714009241303077. doi: 10.1177/19714009241303077.
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.
罗萨伊-多夫曼病(RDD),也称为伴有巨大淋巴结病的窦性组织细胞增多症,是一种罕见的非朗格汉斯细胞组织细胞肿瘤。尽管该疾病典型表现为年轻成年人的无痛性巨大淋巴结病,但在某些患者中RDD也可累及中枢神经系统。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的影像学表现通常类似于脑膜瘤:边界清晰的硬膜下病变,常伴有硬膜尾征。然而,即使在组织病理学确诊之前,也存在一些影像学线索可能有助于放射科医生识别RDD。这份关于中枢神经系统RDD患者的放射学-病理学报告强调了中枢神经系统RDD最相关的临床、影像学和病理学特征,并讨论了神经放射科医生需要了解的关于该疾病的知识。