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Primary HIV infection presenting with Kaposi sarcoma and limbic encephalitis

Authors :
Mathias Fousse
Klaus Fassbender
Sophie Roth
Dominic Kaddu-Mulindwa
Aline Klees-Rollmann
Source :
Journal of NeuroVirology. 26:292-296
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

The development of anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is often associated with neoplasia or infectious diseases as antibodies against neurons or synaptic proteins surface. A 30-year-old male patient was admitted to our department because of neurocognitive symptoms, particularly memory difficulties which had appeared a year prior and since then had been increasing. He had a medical history of smoking and hypertension. On examination, there were no focal neurological deficits. However, neuropsychological tests confirmed a lack of concentration and short-term memory impairment. Brain magnetic resonance imaging (MRI) and electroencephalography (EEG) remained unremarkable. Cerebrospinal fluid (CSF) analysis revealed a low lymphocytic pleocytosis without oligoclonal bands. Serum testing for human immunodeficiency virus (HIV) was positive with 420,000 HIV-1-RNA copies/ml. On a more detailed physical examination, a large number of purple patches were found on the entire body, which a biopsy confirmed to be Kaposi sarcoma (KS). A positive serum and CSF NMDA receptor antibody titer (serum 1:280; CSF 1:8) confirmed the diagnosis of an AIDS-associated anti-NMDA receptor encephalitis; therefore, we treated him with antiretroviral and immunosuppressive therapy. After 12 months, the KS lesions faded and the cognitive deficits improved slightly. Our case highlights that a detailed clinical examination and searching for neoplasia and/or an infection are helpful, though often neglected, tools for detecting an anti-NMDA receptor encephalitis.

Details

ISSN :
15382443 and 13550284
Volume :
26
Database :
OpenAIRE
Journal :
Journal of NeuroVirology
Accession number :
edsair.doi.dedup.....8c61f1114dec517db0ba8c249754e3fb