TY - JOUR
T1 - Fatal autoimmune anti-nmda-receptor encephalitis with poor prognostication score in a young kenyan female
AU - Rakiro, Joe
AU - Sokhi, Dilraj
N1 - Publisher Copyright:
© 2021 Rakiro and Sokhi.
PY - 2021
Y1 - 2021
N2 - Auto-immune N-methyl-D-aspartate receptor encephalitis (NMDARE) is a relatively recently described cause of acute encephalopathy with very few reports from sub-Saharan Africa (SSA). We report a case of NMDARE in a young Kenyan female who was transferred to our facility with headaches, insomnia, behaviour changes and latterly pathog-nomonic orofacial dyskinesias. We comprehensively ruled out infectious and other inflam-matory/auto-immune causes. She was diagnosed with NMDARE by positive antibody testing in serum and cerebrospinal fluid and changes on brain magnetic resonance imaging. She was immunosuppressed with high-dose steroids, intravenous immunoglobulins, plasma exchange and rituximab, and showed signs of neurological improvement clinically and radiologically. Unfortunately, she succumbed to septic shock from prolonged intensive care. This is the first report of NMDARE in an indigenous patient from the eastern SSA. The majority (>80%) of patients are either left with mild disability or make a full recovery after NMDARE, but some factors – which comprise the NMDARE One-Year Functional Status (NEOS) prognostication score – can adversely affect outcome, as was the case in our patient.
AB - Auto-immune N-methyl-D-aspartate receptor encephalitis (NMDARE) is a relatively recently described cause of acute encephalopathy with very few reports from sub-Saharan Africa (SSA). We report a case of NMDARE in a young Kenyan female who was transferred to our facility with headaches, insomnia, behaviour changes and latterly pathog-nomonic orofacial dyskinesias. We comprehensively ruled out infectious and other inflam-matory/auto-immune causes. She was diagnosed with NMDARE by positive antibody testing in serum and cerebrospinal fluid and changes on brain magnetic resonance imaging. She was immunosuppressed with high-dose steroids, intravenous immunoglobulins, plasma exchange and rituximab, and showed signs of neurological improvement clinically and radiologically. Unfortunately, she succumbed to septic shock from prolonged intensive care. This is the first report of NMDARE in an indigenous patient from the eastern SSA. The majority (>80%) of patients are either left with mild disability or make a full recovery after NMDARE, but some factors – which comprise the NMDARE One-Year Functional Status (NEOS) prognostication score – can adversely affect outcome, as was the case in our patient.
KW - Anti-NMDA receptor encephalitis
KW - Auto-immune encephalitis
KW - Sub-Saharan Africa
UR - http://www.scopus.com/inward/record.url?scp=85107272158&partnerID=8YFLogxK
U2 - 10.2147/IMCRJ.S311071
DO - 10.2147/IMCRJ.S311071
M3 - Article
AN - SCOPUS:85107272158
SN - 1179-142X
VL - 14
SP - 343
EP - 347
JO - International Medical Case Reports Journal
JF - International Medical Case Reports Journal
ER -