A rare case of oligoastrocytoma with atypical symptoms initially diagnosed as multiple sclerosis: A case report
Author(s) -
Jiguo Gao,
YANLI TI,
Hongmei Meng,
Teng Zhao,
Chunkui Zhou,
Lijun Zhu,
Shaokuan Fang
Publication year - 2015
Publication title -
molecular and clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.442
H-Index - 7
eISSN - 2049-9469
pISSN - 2049-9450
DOI - 10.3892/mco.2015.686
Subject(s) - medicine , multiple sclerosis , biopsy , cancer , stereotactic biopsy , pathology , dermatology , radiology , immunology
Oligoastrocytoma (OA) is an extremely rare tumor that may be difficult to diagnose, as it mimics multiple sclerosis (MS) clinically and radiologically. OA and MS are both space-occupying lesions. The symptoms of OA are complex and depend on tumor location and size. The clinical symptoms of OA are frequently not typical of glioma; therefore, OA is associated with a high misdiagnosis rate. We herein share our experience with diagnosing a rare OA case with atypical symptoms, which was initially diagnosed as MS, while stereotactic biopsy provided the final diagnosis. Due to the rarity and high misdiagnosis rate of OAs, it is suggested that clinical physicians update their knowledge regarding brain tumor classification and increase their awareness of rare tumor occurrence.
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