Abstract |
We report a young adult with thymoma-associated myasthenia gravis (MG) who, following thymectomy, developed paraneoplastic limbic encephalitis (LE) and systemic lupus erythematosus (SLE). Although thymomas commonly co-occur with MG, LE is an uncommon autoimmune sequela. Herein, we discuss the pathophysiology of paraneoplastic LE and its management. Our report also highlights an unusual case of a thymoma patient who presented with multiple autoimmune disorders. The treatment of such a patient is therefore challenging and requires care from multiple specialized teams.
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Authors | Robin Liu, A Rashid Dar, Keng Yeow Tay, Mike W Nicolle, Richard I Inculet |
Journal | Cureus
(Cureus)
Vol. 10
Issue 11
Pg. e3581
(Nov 13 2018)
ISSN: 2168-8184 [Print] United States |
PMID | 30656085
(Publication Type: Case Reports)
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