| Literature DB >> 28332155 |
Joel S Katz1,2, Pier Paolo Peruzzi1,3, Christopher R Pierson4,5, Jonathan L Finlay3,6, Jeffrey R Leonard7,8.
Abstract
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.Entities:
Keywords: Atypical teratoid rhabdoid tumor; Cerebellopontine angle; Diffuse-weighted imaging
Mesh:
Year: 2017 PMID: 28332155 DOI: 10.1007/s00381-017-3384-3
Source DB: PubMed Journal: Childs Nerv Syst ISSN: 0256-7040 Impact factor: 1.475