1. Multicystic Encephalomalacia: The Neuropathology of Systemic Neonatal Parechovirus Infection
- Author
-
Josephine Heffernan, Pamela O’Connor, Michael B. McDermott, Sara Tone, Suzanne Cronly, Aisling Snow, Cillian De Gascun, Jane B Cryan, Louise Marie Lane, Mary O'Regan, and Ursula Morley
- Subjects
Male ,Pathology ,medicine.medical_specialty ,Parechovirus ,Neuropathology ,Pathology and Forensic Medicine ,03 medical and health sciences ,0302 clinical medicine ,Cerebrospinal fluid ,Encephalomalacia ,Fatal Outcome ,CSF pleocytosis ,030225 pediatrics ,Medicine ,Humans ,Picornaviridae Infections ,biology ,business.industry ,Human parechovirus ,Meninges ,Infant, Newborn ,General Medicine ,medicine.disease ,biology.organism_classification ,medicine.anatomical_structure ,Pediatrics, Perinatology and Child Health ,business ,030217 neurology & neurosurgery ,Encephalitis - Abstract
The Neuropathology of Human Parechovirus (HPeV) is not widely described due to the relatively recent discovery of the virus combined with a limited number of autopsy case reports. We report the case of an infant boy born at 38 weeks who, six days after birth, presented with fever and severe neurological dysfunction. Human Parechovirus Type 3 (HPeV3) RNA was detected in his cerebrospinal fluid (CSF) and blood. He died five days after his initial presentation. Neuropathologic examination demonstrated multicystic encephalomalacia (ME). This case report confirms that white matter pathology is dominant in HPeV3 infection. A unique feature, of HPeV encephalomalacia is absence of CSF pleocytosis and minimal inflammation in the meninges. The findings permit comment on the pathogenesis of brain injury by this virus.
- Published
- 2021