Evidence map›Paper›PMID 42707808›Full record

ReviewNeurosurgery practice2026

Two-Staged Resection of an Infantile Spinal Epidural Teratoma With Intrathoracic Extension: Surgical Case Report With Literature Review.

Tae-Kyun Kim, Yasuhiro Kuroda, Mai Watakabe, Young-Soo Park, Ryota Sasaki, Kenta Nakase, Yudai Morisaki, Ryuta Matsuoka, Shohei Yokoyama, Masashi Kotsugi and 4 more

Abstract readReview
In one paragraph

Review in Neurosurgery practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Tae-Kyun KimDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.ORCID https://orcid.org/0000-0003-2765-7937
Yasuhiro KurodaDepartment of Surgery, Nara Medical University, Kashihara, Nara, Japan.
Mai WatakabeDepartment of Pediatrics, Nara Medical University, Kashihara, Nara, Japan.
Young-Soo ParkDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Ryota SasakiDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Kenta NakaseDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Yudai MorisakiDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Ryuta MatsuokaDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Shohei YokoyamaDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Masashi KotsugiDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Yasuhiro TakeshimaDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Shuichi YamadaDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Fumihiko NishimuraDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.
Ichiro NakagawaDepartment of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesSpinal epidural teratoma (SET) is a rare spinal tumor, particularly in the pediatric population. Because of its rarity and potential for extensive growth into both intraspinal and extraspinal compartments, surgical strategies are not well-standardized. This study aims to describe a successful 2-stage surgical approach for an extensive infantile SET and review the existing literature.

methodsA 1-month-old male infant presented with a large SET extending from T4 to L2 and into the posterior mediastinum. A two-stage surgical approach was performed to achieve gross total resection (GTR). The intraspinal tumor was removed using a split-spinous process laminotomy from T7 to L3. This technique used the natural flexibility of the infant's vertebral arches to create an "open-door" access without detaching the paravertebral muscles. The second surgery was performed 1 month later for the remnant tumor located inside the posterior mediastinal space. The intrathoracic tumor was removed using a thoracoscope with only three 5-mm ports and a small incision for specimen extraction.

resultsHistopathology confirmed a mature teratoma. Postoperative MRI demonstrated GTR. The patient remained neurologically intact and was discharged without respiratory or surgical complications. At the 16-month follow-up, there was no evidence of recurrence or spinal deformity. A literature review identified only 10 previous cases of pediatric SET, highlighting a male predominance and a high frequency of multilevel extension. Paraparesis was common in most cases, whereas 2 infants presented with dyspnea because of mediastinal compression. Histologically, all except 1 case were mature teratomas, and all cases treated with GTR remained recurrence-free.

conclusionGTR is the gold standard for pediatric SET because of its histologically mature nature. A staged approach with "open-door" split-spinous process laminotomy and thoracoscopic surgery was an effective strategy. Reducing surgical stress is essential in fragile infants with extensive SETs.

Indexed as

Intrathoracic extensionMultistaged surgeryPediatricSpinal epidural teratomaThoracoscopic surgery

Identifiers

PMID42707808
PMCPMC13549624

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.