Evidence map›Paper›PMID 38505775›Full record

ArticleFrontiers in neuroscience2024

Case report: Febrile infection-related epilepsy syndrome in a 14-year-old girl with multiple organ failure and lethal outcome.

Lars Ruttkowski, Ines Wallot, Marie Korell, Elke Daur, Peter Seipelt, Andreas Leonhardt, Stefanie Weber, Nadine Mand

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In one paragraph

Article in Frontiers in neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Lars RuttkowskiPediatric Intensive Care, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.
Ines WallotPediatric Neurology, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.
Marie KorellPediatric Intensive Care, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.
Elke DaurPediatric Intensive Care, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.
Peter SeipeltPediatric Neurology, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.
Andreas LeonhardtPediatric Intensive Care, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.
Stefanie WeberPediatric Nephrology, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.
Nadine MandPediatric Intensive Care, Department of Pediatrics, Philipps-University Marburg, Marburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a case of an otherwise healthy 14-year-old girl with febrile infection-related epilepsy syndrome (FIRES), multiple organ failure (MOF), and ultimately a lethal outcome. This is a rare case of FIRES with MOF and consecutive death. Only a few cases have been described in the literature. The adolescent girl was initially admitted to our pediatric emergency department with a first episode of generalized tonic-clonic seizures after a short history of fever a week before admission. Seizures progressed rapidly into refractory status epilepticus without any evidence of the underlying cause, and treatment subsequently had to be escalated to thiopental anesthesia. Since the initial diagnostics showed no promising leads, the rare syndrome of FIRES was suspected, representing a catastrophic epileptic encephalopathy linked to a prior benign febrile infection. Methylprednisolone, intravenous immunoglobulins, and a ketogenic diet were initiated. Respiratory, circulatory, kidney, and liver failure developed during treatment, requiring increasing intensive care. Multiple attempts to deescalate antiepileptic treatment resulted in recurrent status epilepticus. A cranial MRI on the 10th day of treatment revealed diffuse brain edema and no cerebral perfusion. The patient was declared dead on the 11th day of treatment. FIRES should be taken into account in previously healthy children with a new onset of difficult-to-treat seizures after a short febrile infection when no other cause is apparent. First-line treatment, besides seizure control, is the early initiation of immunomodulatory therapy and the start of a ketogenic diet. As treatment is difficult and MOF may develop, patients should be transferred to a specialized children's hospital providing full intensive care.

Indexed as

FIRESmultiple organ failureNORSEpediatric neurologypediatric status epilepticus

Identifiers

PMID38505775
PMCPMC10948546

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.