Desmoplastic infantile ganglioglioma is a rare intracranial tumor of early childhood with a usually excellent prognosis despite malignant features both radiologically and histologically. We present the case of a desmoplastic infantile ganglioglioma with histologically highly anaplastic features and both intracerebral and pial metastases. After partial resection the tumor was rapidly progressive and new metastases appeared. A combination of vincristine and carboplatinum was used according to the Low Grade Glioma Protocol of the International Society of Pediatric Oncology, with a temporary good response. When histologically characterized by highly anaplastic features, it seems the biologic behavior of this tumor remains uncertain. The aggressive behavior and the responsiveness to chemotherapy in this case may challenge the belief in the benign nature of these rare tumors.
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http://dx.doi.org/10.1097/00000478-200211000-00015 | DOI Listing |
Asian J Surg
October 2024
Department of Neurosurgery, Lanzhou University Second Hospital, Lanzhou, Gansu Province, China. Electronic address:
Clin Case Rep
August 2024
Multiple Sclerosis Research Center, Neuroscience Institute Tehran University of Medical Sciences Tehran Iran.
Here we present a co-occurrence of a non-typical presentation of DIG/DIA and multiple sclerosis in a 13-year-old female. Our case highlights how a thorough investigation prior to treatment is needed in patients with such condition to choose proper management for better prognosis.
View Article and Find Full Text PDFActa Neuropathol Commun
July 2024
Department of Pathology, Seoul National University College of Medicine, 101 Daehak-Ro, Jongno-Gu, Seoul, Republic of Korea.
Childs Nerv Syst
October 2024
Department of Neurosurgery, The Royal Children's Hospital, Melbourne, Australia.
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