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Diagnosis and treatment for pure aqueductal tumor
Institution:1. Department of Neurosurgery, Kanazawa Medical University, 1-1 Daigaku, Uchinada 920-0293, Ishikawa, Japan;2. Department of Diabetology and Endocrinology, Kanazawa Medical University, Ishikawa, Japan;3. Department of Pathology and Laboratory Medicine, Kanazawa Medical University, Ishikawa, Japan;1. Division of Pediatric Neurosurgery, Department of Neurosurgery, Seoul National University Children''s Hospital, Seoul, Republic of Korea;2. Department of Neurosurgery, Seoul National University Hospital, Seoul, Republic of Korea;3. Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea;1. School of Medicine, University of Liverpool, Liverpool, United Kingdom;2. Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom;3. Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom;4. Department of Neurosurgery, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom;5. Department of Neuropathology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom;6. Department of Neuroradiology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom;1. Department of Neurosurgery, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Manchester Academic Health Sciences Centre, Salford, Greater Manchester, UK;2. Complex NF1 Service, Manchester Centre for Genomic Medicine, St Mary’s Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK;3. Division of Evolution and Genomic Sciences, School of Biological Sciences, University of Manchester, Manchester Academic Health Sciences Centre, Manchester, UK;4. Neuropathology Unit, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Manchester Academic Health Sciences Centre, Salford, Greater Manchester, UK;5. Division of Neuroscience & Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK;6. Department of Neuroradiology, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Manchester Academic Health Sciences Centre, Salford, Greater Manchester, UK;1. Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy;2. Department of Neurosurgery, Humanitas Clinical and Research Center IRCCS, Rozzano, Milan, Italy
Abstract:Pure aqueductal tumor (PAT) typically originates from pure aqueductal region and is extremely rare. It is radiographically similar to tectal glioma. We examined two patients with PATs who were diagnosed with pilocytic astrocytoma and rosette-forming glioneuronal tumor. Both cases showed a progressive clinical course. It is important to distinguish between PAT and tectal glioma by radiographic imaging because the treatment strategy is different. While observation is common for tectal gliomas, a biopsy is recommended at the same time of endoscopic third ventriculostomy for PAT with hydrocephalus. Low-grade PATs show an aggressive clinical course in some cases. Our two cases also showed aggressive course in spite of no genetic aggressive mutations. Sagittal view by constructive interference in steady state (CISS) imaging was helpful to make an accurate diagnosis of PAT. Close observation is needed if PAT is diagnosed as low-grade tumor.
Keywords:Aqueduct  Tectum  ETV  BRAF V600E  IDH1
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