Katz Joel S, Peruzzi Pier Paolo, Pierson Christopher R, Finlay Jonathan L, Leonard Jeffrey R
Division of Pediatric Neurosurgery, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH, 43205, USA.
Department of Neurosurgery, Grant Medical Center, Columbus, OH, USA.
Childs Nerv Syst. 2017 May;33(5):833-838. doi: 10.1007/s00381-017-3384-3. Epub 2017 Mar 22.
Atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system (CNS) are rare, highly malignant neoplasms that carry a poor prognosis. Even with prompt diagnosis, gross total resection and early initiation of intensive adjuvant therapy, the majority of patients will succumb within 9-12 months of diagnosis. The CPA location in children harbors lesions along a wide spectrum varying from benign to highly malignant. Imaging features of lesions within the CPA that aid the diagnostic process will help to initiate early treatment in higher-grade lesions. We report three cases, in very young children, all with cranial nerve deficits, who displayed CPA lesions with restricted diffusion on diffusion-weighted imaging (DWI) with pathology confirming AT/RT. We propose that in young children with a CPA tumor diffusion-weighted imaging should be routinely evaluated to aid in prompt management. In addition, the diagnosis of AT/RT should be highly suggestive in infants presenting with cranial nerve findings as well as DWI restricted diffusion within the CPA.
中枢神经系统(CNS)的非典型畸胎样/横纹肌样肿瘤(AT/RT)是罕见的高度恶性肿瘤,预后较差。即使能迅速诊断、进行全切除并尽早开始强化辅助治疗,大多数患者在确诊后9至12个月内仍会死亡。儿童CPA部位的病变范围广泛,从良性到高度恶性都有。有助于诊断过程的CPA内病变的影像学特征将有助于对高级别病变尽早进行治疗。我们报告了3例非常年幼的儿童病例,均有颅神经功能缺损,其CPA病变在扩散加权成像(DWI)上表现为扩散受限,病理证实为AT/RT。我们建议,对于患有CPA肿瘤的幼儿,应常规评估扩散加权成像,以帮助及时处理。此外,对于出现颅神经症状且CPA内DWI扩散受限的婴儿,应高度怀疑AT/RT的诊断。