Pineoblastomas, which originate from the pineal gland, are extremely malignant tumors that grow quickly and aggressively. Because they spread so fast and the probability of longterm survival is poor, it is important to diagnose these tumors early. This article discusses magnetic resonance's role in imaging pineoblastomas. MR is particularly effective for this task due to its ability to visualize the pineoblastoma in three different planes, both before and after the administration of gadolinium.
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Zhonghua Er Ke Za Zhi
January 2025
Department of Medical Oncology, Pediatric Oncology Center,Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, National Key Clinical Discipline of Pediatric Oncology,Laboratory for Clinical Medicine, Capital Medical University, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing100045, China.
Neurology
November 2024
From the Departments of Neurosurgery (R.Z., X.H., S.Z.), Cardiovascular Surgery (J.L.), West China Hospital of Sichuan University.
J Pak Med Assoc
March 2024
Department of Neurosurgery, The Aga Khan University, Karachi, Pakistan.
BMJ Case Rep
July 2024
Pediatrics, Children's Hospital Orange County, Orange, Florida, USA
Neuro Oncol
December 2024
Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Pineal parenchymal tumors are rare neoplasms for which evidence-based treatment recommendations are lacking. These tumors vary in biology, clinical characteristics, and prognosis, requiring treatment that ranges from surgical resection alone to intensive multimodal antineoplastic therapy. Recently, international collaborative studies have shed light on the genomic landscape of these tumors, leading to refinement in molecular-based disease classification in the 5th edition of the World Health Organization (WHO) classification of tumors of the central nervous system.
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