Background/aim: Mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) is a rare clinicoradiological syndrome that typically presents with central nervous system symptoms such as loss of consciousness, seizure, headache, and ophthalmoparesis. Materials and methods: Here, we highlight the characteristics of this syndrome together with the clinical and MRI findings of 6 pediatric patients with MERS. Results: Between January 2017 and October 2020, 6 patients with MERS (3 boys and 3 girls) presented to our center. The mean age was 122 ± 54.6 (min-max: 44-180) months. None of the patients had a chronic disease. In our study, infectious agents were detected in 4 patients (66.6%), while noninfectious causes (one seizure and the other hyponatremia) were detected in two patients. All of our cases were discharged without any sequelae after an average of 12.1 ± 7 (min-max: 4-20) days of hospitalization. In 1 patient (case 6), control MRI could not be performed, and the radiological recovery of our other patients was shown to be between 14 days and 2 months. Conclusion: MERS is an acute encephalopathy with good prognosis and should be considered by neurologists in differential diagnosis due to its variable clinical presentation and specific MRI findings.
MERS, childhood, treatment, prognosis
ÇELİK, HALİL; DERİNKUYU, BETÜL EMİNE; AKSOY, ERHAN; ÖZTOPRAK, ÜLKÜHAN; CEYLAN, NESRİN; AZAPAĞASI, EBRU; ÖZDEM, SUNA; OĞUZ, MELAHAT MELEK; and YÜKSEL, DENİZ
"Clinically mild encephalitis/encephalopathy with a reversible splenial lesion of thecorpus callosum in childhood: a single-center experience,"
Turkish Journal of Medical Sciences: Vol. 52:
2, Article 15.
Available at: https://journals.tubitak.gov.tr/medical/vol52/iss2/15