Yeh E Ann, Greenberg Jay, Abla Oussama, Longoni Giulia, Diamond Eli, Hermiston Michelle, Tran Brandon, Rodriguez-Galindo Carlos, Allen Carl E, McClain Kenneth L
Department of Neurology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Center for Cancer and Blood Disorders, Children's National Medical Center, Washington, District of Columbia.
Pediatr Blood Cancer. 2018 Jan;65(1). doi: 10.1002/pbc.26784. Epub 2017 Sep 25.
Central nervous system (CNS) involvement in Langerhans cell histiocytosis (LCH) can include mass lesions of the hypothalamic pituitary axis, choroid plexus, cerebrum, and cerebellum or magnetic resonance imaging (MRI) signal abnormalities of the cerebellum, pons, and basal ganglia. The term neurodegenerative (ND) CNS-LCH has been given to the MRI signal abnormalities and neurologic dysfunction, although initially patients may have no clinical symptoms. Standardized evaluations to better understand the natural history and response to therapy are needed. We propose guidelines for clinical, radiologic, and physiologic tests as a framework for developing the best methods of evaluation, which can then be tested in prospective treatment protocols.
朗格汉斯细胞组织细胞增多症(LCH)累及中枢神经系统(CNS)可表现为下丘脑 - 垂体轴、脉络丛、大脑和小脑的肿块性病变,或小脑、脑桥和基底节的磁共振成像(MRI)信号异常。尽管最初患者可能没有临床症状,但MRI信号异常和神经功能障碍被称为神经退行性(ND)CNS - LCH。需要进行标准化评估以更好地了解其自然病史和对治疗的反应。我们提出临床、放射学和生理学检查的指南,作为开发最佳评估方法的框架,然后可在前瞻性治疗方案中进行测试。