Evidence map›Paper›PMID 41409871›Full record

ArticleSurgical neurology international2025

A rare case of cauda equina paraganglioma histologically simulating ependymoma.

Ebrahim Mohamd Kher Alyousef, Bashayer Abdulla Alshamsi, Mahra Ali Almazrouei, Ammar Shahid Tanweer, Tasnim Ebrahem Alyousef, Elaf Ebrahem Alyousef

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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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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ebrahim Mohamd Kher AlyousefDepartment of Neurosurgery, Saqr Hospital, Ras Al Khaimah, United Arab Emirates.
Bashayer Abdulla AlshamsiDepartment of medicine, Sheikh Shakhbout Medical City SSMC, Abudhabi, United Arab Emirates.
Mahra Ali AlmazroueiDepartment of Medicine, Mohammed Bin Rashid University MBRU, Dubai, United Arab Emirates.
Ammar Shahid TanweerDepartment of Medicine, Mohammed Bin Rashid University MBRU, Dubai, United Arab Emirates.
Tasnim Ebrahem AlyousefDepartment of Medicine, Gaziantep University, Gaziantep, Turkey.
Elaf Ebrahem AlyousefDepartment of Medicine, Gaziantep University, Gaziantep, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Paragangliomas of the cauda equina are rare neuroendocrine tumors that can mimic ependymomas on imaging and histology, creating diagnostic challenges and influencing surgical planning. Case Description: A 41-year-old man presented with progressive low back pain and bilateral leg numbness. MRI showed a well-circumscribed, enhancing intradural extramedullary mass at L3. He underwent L3-L4 laminectomy with gross-total microsurgical excision. Histopathology revealed pseudorosettes and uniform tumor cells, initially suggesting ependymoma; however, immunohistochemistry demonstrated strong synaptophysin and S100 positivity with negative GFAP and EMA, confirming a cauda equina paraganglioma. Postoperatively, the patient recovered fully and remained asymptomatic at 1-year follow-up. Conclusion: Paragangliomas can closely resemble ependymomas, and accurate diagnosis requires immunohistochemistry. Complete surgical excision yields excellent outcomes, and individualized long-term imaging follow-up is recommended because recurrence, although uncommon, can occur.

Indexed as

Cauda equineEpendymomaImmunohistochemistryNeurosurgeryParagangliomaSpinal tumor

Identifiers

PMID41409871
PMCPMC12707721

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