Primary neurolymphomatosis with MAG antibody: a case report
Neurolymphomatosis (NL) is a rare neurologic manifestation of non-Hodgkin lymphoma (NHL) with poor prognosis. Investigations including MRI, PET/CT, nerve biopsy and cerebrospinal fluid (CSF) analysis can aid the diagnosis of NL. In this study, we presented a case of NL with co-existing myelin-associated glycoprotein (MAG) antibody. The patient first presented with symptoms of peripheral neuropathy involving multiple cranial nerves and cauda equina, and later developed obstructive hydrocephalus and deep matter lesions. He also had persistently positive MAG antibody, but did not develop electrophysiologically proven neuropathy and monoclonal immunoglobulin. The final brain biopsy confirmed diffuse large B cell lymphoma.
Authors
- Yue‐Bei Luo (ORCID: https://orcid.org/0000-0002-1056-0154)
- Huan Yang (ORCID: https://orcid.org/0000-0002-8690-2544)
- Jing Li (ORCID: https://orcid.org/0000-0002-4021-7111)
- Si Chen (ORCID: https://orcid.org/0000-0003-4339-5340)
- Honglian Zhang (ORCID: https://orcid.org/0000-0002-6822-5359)
Institutions
- Central South University (CN)
- First Affiliated Hospital of Jiangxi Medical College (CN)
- Jiangxi Provincial People's Hospital (CN)
- Xiangya Hospital Central South University (CN)
Publication Details
- Journal
- BMC Neurology
- Published
- 2024-09-05
- DOI
- https://doi.org/10.1186/s12883-024-03798-7
- Primary Topic
- CNS Lymphoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Health Commission of Jiangxi Province