Evidence map›Paper›PMID 40837301›Full record

ArticleSurgical neurology international2025

Symptomatic pseudotumor in Meckel cave mimics trigeminal schwannoma.

Tomoya Sofue, Megumi Chatani, Yoshihiro Kuga, Hiroyuki Ohnishi

Abstract readCase Reports
In one paragraph

Article in Surgical neurology international, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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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5 · Who and what money

Authors and funding

4 authors.

Tomoya SofueDepartment of Neurosurgery, Ohnishi Neurological Center, Akashi, Hyogo, Japan.
Megumi ChataniDepartment of Neurosurgery, Ohnishi Neurological Center, Akashi, Hyogo, Japan.
Yoshihiro KugaDepartment of Neurosurgery, Ohnishi Neurological Center, Akashi, Hyogo, Japan.
Hiroyuki OhnishiDepartment of Neurosurgery, Ohnishi Neurological Center, Akashi, Hyogo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Inflammatory pseudotumor is non-neoplastic lesions that form tumor-like masses, typically occurring in the lungs and orbits, with rare involvement of intracranial regions such as the Meckel cave. While neuroimaging can assist in differential diagnosis, definitive diagnosis may remain challenging. Some cases are associated with immunoglobulin G4 (IgG4)-related disease, highlighting the importance of histopathological confirmation to guide appropriate management. Case Description: A case of a 42-year-old woman presented with facial numbness and headache. Magnetic resonance imaging revealed a 25-mm enhancing mass in the left Meckel cave, initially suspected to be a trigeminal schwannoma. Craniotomy and tumor resection were performed. Intraoperative findings and rapid pathology indicated marked inflammatory cell infiltration without features of schwannoma. The final diagnosis was inflammatory pseudotumor, with no evidence of IgG4-related disease or malignancy. Postoperative symptoms improved, and only a short course of steroids was administered. Conclusion: This case underscores the diagnostic difficulty of distinguishing inflammatory pseudotumor from neoplastic lesions in skull base regions. Surgical biopsy or resection is critical for definitive diagnosis, especially in cases with progressive symptoms. Individualized treatment planning based on disease activity and neurological impact remains essential due to the absence of standardized treatment guidelines.

Indexed as

Meckel cavePathological diagnosisPseudotumorTrigeminal schwannoma

Identifiers

PMID40837301
PMCPMC12361671

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