| Literature DB >> 29915889 |
Noriyuki Watanabe1, Haruo Ohtani2, Shuichi Mori1, Masahiro Iguchi1, Alexander Zaboronok3, Noriaki Sakamoto4, Masahide Matsuda3, Eiichi Ishikawa5, Akira Matsumura3.
Abstract
Although liposarcomas are the most common soft tissue sarcomas, their intracranial variants are extremely rare. Here, we present a case of a primary intracranial myxoid liposarcoma in a 23-year-old Japanese man who presented with generalized seizures and a mass in the left frontal lobe. The tumor was totally removed, and histological analyses pointed to liposarcoma. Thirteen years after his initial treatment, the patient presented with right-side weakness and local recurrence of tumor was discovered. Histology from the second resection confirmed the diagnosis of myxoid liposarcoma. Shortly after the second resection, progressive, new intracranial lesions were observed and despite a third resection, extensive intracerebral invasion by the tumor proved fatal. The histological features of myxoid liposarcoma were essentially similar with each recurrence, but the aggressive tumor behavior after the second operation did not align with expectations based on histological classification.Entities:
Keywords: Intracranial; Myxoid liposarcoma; Primary tumor; Recurrence
Mesh:
Year: 2018 PMID: 29915889 DOI: 10.1007/s00701-018-3598-5
Source DB: PubMed Journal: Acta Neurochir (Wien) ISSN: 0001-6268 Impact factor: 2.216