Antibody‐Negative Paraneoplastic Limbic Encephalitis, Parkinsonism, Hypothermia, and Narcolepsy Associated with Endometrial Carcinoma

Abstract

Background Background: We describe the clinical and neuropathological features of a patient with T-cellmediated paraneoplastic limbic encephalitis, parkinsonism, hypothermia, and narcolepsy-like presentation associated with endometrial carcinoma. Objectives Objectives: This patient with prominent parkinsonism and narcolepsy broadens the phenotype of known paraneoplastic syndromes and demonstrates the importance of investigation for occult malignancy even in the absence of paraneoplastic antibodies. Methods Methods: This is a case report with diagnosis confirmed at postmortem. ResultsResults: Paraneoplastic antibodies were not detected. The initial improvement with immunosuppression was short lived, and postmortem neuropathological examination demonstrated encephalitis with predominant T-cell infiltration affecting the hypothalamus and extending to the brainstem, suggestive of a paraneoplastic syndrome. ConclusionsConclusions: Although the possibility of a novel antibody cannot be ruled out, consideration must also be given to recent demonstration of purely T-cell-mediated neuronal destruction in the context of paraneoplastic syndromes.

What’s New in Narcolepsy? Review of All Published Literature in 2020

“…Novel antibodies related to paraneoplastic syndromes should be studied or reported and can not be ruled out as suggested by authors [15] appeared to be suitable and efficient instruments for assessing HRQoL in PWN [30]. Chang., et al in their case control study reported significantly increased risk of narcolepsy patients to burn injury compared to unaffected controls.…”