A Pediatric Case of Late Relapse of Neonatal Herpes Simplex Encephalitis in a 14-Year-Old

Authors

  • Kevin Jiang UT Health San Antonio, Department of Radiology, San Antonio, USA
  • Sally Choi UT Health San Antonio, Department of Radiology, San Antonio, USA
  • Carlos Bazan UT Health San Antonio, Department of Radiology, San Antonio, USA
  • Andrea Gilbert UT Health San Antonio, Department of Pathology, San Antonio, USA
  • Jason Lally UT Health San Antonio, Department of Pathology, San Antonio, USA

DOI:

https://doi.org/10.3941/jrcr.5495

Abstract

Herpes simplex encephalitis is the most common type of viral encephalitis. However, recurrence or relapse is rare. Late relapse, defined as recurrent active infection later than 3 months from the end of antiviral treatment, is even rarer. The following case illustrates the longest recorded idiopathic late relapse of herpes simplex encephalitis with biopsy-proven confirmation on histopathology. The literature suggests multiple mechanisms for relapse including latent reactivation, post-infectious autoimmune disease, and genetic predisposition. Regardless, untreated recurrent herpes simplex encephalitis has a high morbidity and mortality, and it is the only etiology of viral encephalitis with an effective anti-viral treatment. As such, it should remain an important consideration on the differential diagnosis of encephalitis for prompt recognition and timely management.

 

14 year old female with recurrent HSV encephalitis

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Published

2025-01-31

Issue

Section

Neuroradiology