Acute hemorrhagic leukoencephalitis of Weston Hurst secondary to herpes encephalitis presenting as status epilepticus: A case report and review of literature
•Acute hemorrhagic leukoencephalitis is a rare and fatal demyelinating disease.•This case presented a patient with an intracerebral hemorrhage in status epilepticus.•Treatment with high-dose methylprednisolone prevented mortality. Acute hemorrhagic leukoencephalitis (AHL) is a rare and mostly fatal...
Saved in:
Published in: | Journal of clinical neuroscience Vol. 67; pp. 265 - 270 |
---|---|
Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Scotland
Elsevier Ltd
01-09-2019
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | •Acute hemorrhagic leukoencephalitis is a rare and fatal demyelinating disease.•This case presented a patient with an intracerebral hemorrhage in status epilepticus.•Treatment with high-dose methylprednisolone prevented mortality.
Acute hemorrhagic leukoencephalitis (AHL) is a rare and mostly fatal fulminant demyelinating disease. This case describes a 63-year old male in status epilepticus associated with an intracerebral hemorrhage following a one week viral prodrome with rapid decline to coma. He exhibited peripheral leukocytosis, neutrophilic pleocytosis with normal glucose and high protein in cerebrospinal fluid (CSF). Additionally, CSF was positive for herpes simplex virus (HSV) polymerase chain reaction (PCR). Medical decompression, low-dose dexamethasone, antibiotics and acyclovir were initially given. Magnetic resonance imaging (MRI) was suggestive of AHL, thus he was treated with methylprednisolone 1 g/day for 5 days. The patient improved and was discharged with significant neurologic morbidity. This is the first reported case of AHL in the Philippines presenting as a diagnostic dilemma with a protracted clinical course who responded to high dose intravenous steroids. |
---|---|
Bibliography: | ObjectType-Case Study-3 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Review-1 ObjectType-Feature-5 ObjectType-Report-2 ObjectType-Article-4 |
ISSN: | 0967-5868 1532-2653 |
DOI: | 10.1016/j.jocn.2019.06.020 |