Evidence map›Paper›PMID 36910634›Full record

ArticleFrontiers in oncology2023

Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review.

Giulio Bonomo, Alessandro Gans, Elio Mazzapicchi, Emanuele Rubiu, Paolo Alimonti, Marica Eoli, Rosina Paterra, Bianca Pollo, Guglielmo Iess, Francesco Restelli and 5 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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

15 authors.

Giulio BonomoDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Alessandro GansDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Elio MazzapicchiDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Emanuele RubiuDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Paolo AlimontiDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Marica EoliMolecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Rosina PaterraMolecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Bianca PolloNeuropathology Unit, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Guglielmo IessDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Francesco RestelliDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Jacopo FalcoDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Francesco AcerbiDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Marco Paolo SchiaritiDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Paolo FerroliDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Morgan BroggiDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sporadic Spinal Psammomatous Malignant Melanotic Nerve Sheath Tumor (SSP-MMNST) is a rare subgroup of peripheral nerve sheath tumors arising along the spine. Only a few reports of SSP-MMNST have been described. In this paper, we review the literature on SSP-MMNST focusing on clinical, and diagnostic features, as well as investigating possible pathogenetic mechanisms to better implement therapeutic strategies. We also report an illustrative case of a young female presenting with cervicobrachial pain due to two SSP-MMNSTs arising from C5-6 right spinal roots. Case description: We report a case of a 28-year-old woman presenting with right arm weakness and dysesthesia. Clinical examination and neuroimaging were performed, and, following surgical removal of both lesions, a histological diagnosis of SSP-MMNST was obtained. Results: The literature review identified 21 eligible studies assessing 23 patients with SSP-MMNST, with a mean onset age of 41 years and a slight male gender preference. The lumbar district was the most involved spinal segment. Gross-total resection (GTR) was the treatment of choice in all amenable cases, followed in selected cases with residual tumor by adjuvant radiotherapy or chemotherapy. The metastatic and recurrence rates were 31.58% and 36.8%, respectively. Conclusion: Differently from common schwannomas, MMNST represents a rare disease with known recurrence and metastatization propensity. As reported in our review, SSP-MMNST has a greater recurrence rate when compared to other forms of spinal MMNST, raising questions about the greater aggressiveness of the former. We also found that residual disease is related to a higher risk of systemic disease spreading. This metastatic potential, usually associated with primary lumbar localization, is characterized by a slight male prevalence. Indeed, whenever GTR is unachievable, considering the higher recurrence rate, adjuvant radiation therapy should be taken into consideration.

Indexed as

case reportmalignant melanotic nerve sheath tumormelanotic schwannomanerve sheathpsammomatousspinalsporadictumor

Identifiers

PMID36910634
PMCPMC9998981

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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.