Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Neurological Medicine
Volume 2017 (2017), Article ID 9131579, 4 pages
https://doi.org/10.1155/2017/9131579
Case Report

Evolution of Cerebral Atrophy in a Patient with Super Refractory Status Epilepticus Treated with Barbiturate Coma

1Department of Neurology, University of Missouri, 5 Hospital Drive, CE 540, Columbia, MO 65211, USA
2Cleveland Clinic, Department of Neurology, Cerebrovascular Center, 9500 Euclid Avenue, Cleveland, OH 44125, USA
3Cleveland Clinic, Department of Pharmacy, 9500 Euclid Avenue, Cleveland, OH 44125, USA
4Cleveland Clinic, Department of Neurology, Epilepsy Center, 9500 Euclid Avenue, Cleveland, OH 44125, USA
5Wake Forest University School of Medicine, Neurology and Critical Care (Anesthesia), Reynolds M, Medical Center Blvd, Winston Salem, NC 27157, USA

Correspondence should be addressed to Christopher R. Newey; ude.iruossim.htlaeh@cyewen

Received 30 August 2016; Revised 1 December 2016; Accepted 12 December 2016; Published 15 January 2017

Academic Editor: Samuel T. Gontkovsky

Copyright © 2017 Christopher R. Newey et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Introduction. Status epilepticus is associated with neuronal breakdown. Radiological sequelae of status epilepticus include diffusion weighted abnormalities and T2/FLAIR cortical hyperintensities corresponding to the epileptogenic cortex. However, progressive generalized cerebral atrophy from status epilepticus is underrecognized and may be related to neuronal death. We present here a case of diffuse cerebral atrophy that developed during the course of super refractory status epilepticus management despite prolonged barbiturate coma. Methods. Case report and review of the literature. Case. A 19-year-old male with a prior history of epilepsy presented with focal clonic seizures. His seizures were refractory to multiple anticonvulsants and eventually required pentobarbital coma for 62 days and midazolam coma for 33 days. Serial brain magnetic resonance imaging (MRI) showed development of cerebral atrophy at 31 days after admission to our facility and progression of the atrophy at 136 days after admission. Conclusion. This case highlights the development and progression of generalized cerebral atrophy in super refractory status epilepticus. The cerebral atrophy was noticeable at 31 days after admission at our facility which emphasizes the urgency of definitive treatment in patients who present with super refractory status epilepticus. Further research into direct effects of therapeutic coma is warranted.