Evidence map›Paper›PMID 38742265›Full record

ArticleBrain tumor research and treatment2024

Pediatric Eosinophilic Granuloma Associated With Delayed Epidural Hematoma Following on Seizure: A Case Report.

Hyun Jeong Cho, Sung Chan Park, Jong Min Lee, Na Young Jung, Jun Bum Park

Abstract readCase Reports
In one paragraph

Article in Brain tumor research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers 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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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hyun Jeong ChoDepartment of Neurosurgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.ORCID https://orcid.org/0009-0007-7566-4628
Sung Chan ParkDepartment of Neurosurgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.ORCID https://orcid.org/0000-0003-2660-3611
Jong Min LeeDepartment of Neurosurgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.ORCID https://orcid.org/0000-0003-2324-8706
Na Young JungDepartment of Neurosurgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.ORCID https://orcid.org/0000-0001-9996-1378
Jun Bum ParkDepartment of Neurosurgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea. parkjb@uuh.ulsan.kr.ORCID https://orcid.org/0000-0001-6005-9221

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic granuloma (EG), a subtype of Langerhans cell histiocytosis (LCH), the monostotic form, is a rare condition characterized by a solitary bone lesion. It is even more unusual for this condition to be accompanied by an epidural hematoma (EDH). This case is unique in that it is the first to involve delayed EDH following a seizure. We describe a remarkable example of EG accompanied by an EDH and consider the rarity of this comorbidity. A 32-month-old boy developed a rapidly growing skull mass following a minor head injury. During surgical preparation for a biopsy, the patient experienced a single convulsion. Imaging following the seizure revealed an EDH in the vicinity of the mass. The mass was excised and confirmed to be an EG, but with positive margins. The patient underwent chemotherapy after systemic skeletal evaluation, in accordance with the LCH III protocol established by the Histiocytosis Society. EG is a rare neoplasm that typically presents as a painless growth on the skull that gradually enlarges over time. The correlation between EG and EDH is exceedingly uncommon, with only a few documented cases. This case study underscores the significance of considering EG in the differential diagnosis of an expanding cranium mass, even when associated with EDH. Prompt diagnosis and treatment can prevent serious complications and improve patient outcomes.

Indexed as

Case reportCerebral hemorrhageEosinophilic granulomaHistiocytosisLangerhans-cellSeizures

Identifiers

PMID38742265
PMCPMC11096632

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