Evidence map›Paper›PMID 40255923›Full record

ArticleNMC case report journal2025

Thoracic Intradural Extramedullary Cavernous Malformation Mimicking Meningioma.

Takanori Fukunaga, Shingo Toyota, Tomoaki Murakami, Shuki Okuhara, Teruaki Nagano, Kosei Okochi, Koichi Nakashima, Motoki Nakamura, Shuhei Yamada, Takamune Achiha and 2 more

Abstract readCase Reports
In one paragraph

Article in NMC case report journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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

12 authors.

Takanori FukunagaDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Shingo ToyotaDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Tomoaki MurakamiDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Shuki OkuharaDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Teruaki NaganoDepartment of Pathology, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Kosei OkochiDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Koichi NakashimaDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Motoki NakamuraDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Shuhei YamadaDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Takamune AchihaDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Maki KobayashiDepartment of Neurosurgery, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
Haruhiko KishimaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cavernous malformation, also known as cavernoma or cavernous hemangioma, is a benign vascular malformation characterized by abnormal proliferation of capillaries that lack intervening neural tissue. Spinal intradural extramedullary cavernous malformations are exceedingly rare and, therefore, are often misdiagnosed. Here, we report a rare case of thoracic intradural extramedullary cavernous malformation that mimicked meningioma on preoperative imaging. A 77-year-old male patient presented with a two-month history of myelopathy, progressive paresthesia in the lower extremities, and difficulty walking, noted during an outpatient clinic visit. Spinal magnetic resonance imaging detected an intradural extramedullary mass lesion on the dorsal side at the Thoracic (Th) 10 vertebral level, compressing the thoracic cord. Preoperative imaging revealed a uniform T1- and T2-weighted intensity signal, suggesting meningioma. Intraoperatively, the mass appeared reddish with multiple abnormal vessels and adhered firmly to the thoracic cord. The lesion was completely resected, and postoperative pathological examination confirmed the diagnosis of cavernous malformation. The patient's preoperative symptoms improved postoperatively. Thoracic intradural extramedullary cavernous malformations are extremely rare and typically present with heterogeneous intensity signals on magnetic resonance imaging. Additionally, they can cause subarachnoid hemorrhage, emphasizing the importance of considering them in the preoperative differential diagnosis, even though imaging characteristics may be atypical. Surgical gross total resection should be considered to prevent future hemorrhage and neurological deterioration.

Indexed as

cavernous malformationextramedullaryintraduralmyelopathythoracic

Identifiers

PMID40255923
PMCPMC12009646

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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.