Evidence map›Paper›PMID 32698273›Full record

ArticleInternational journal of surgery case reports2020

Intraosseous schwannoma of the femur in a patient with monoclonal gammopathy of undetermined significance.

Timothy McAleese, Kevin Clesham, Darren Moloney, Andrew Hughes, Nazia Faheem, Khalid Merghani

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2020. 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
0.5field-weighted citation impact, top 30% of its field
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, 10 citations in OpenAlex.

  1. Review
  2. Intraosseous schwannoma of distal femur: A case report.International journal of surgery case reports · 2022
    Article
  3. Article
  4. Article
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

6 authors at 1 institution in 1 country.

Timothy McAleeseNational University of Ireland, Galway, Co. Galway, Ireland; Department of Trauma and Orthopaedics, Midland Regional Hospital Tullamore, Tullamore, Co. Offaly, Ireland. Electronic address: t.mcaleese1@nuigalway.ie.
Kevin CleshamDepartment of Trauma and Orthopaedics, Midland Regional Hospital Tullamore, Tullamore, Co. Offaly, Ireland.
Darren MoloneyDepartment of Trauma and Orthopaedics, Midland Regional Hospital Tullamore, Tullamore, Co. Offaly, Ireland.
Andrew HughesDepartment of Trauma and Orthopaedics, Midland Regional Hospital Tullamore, Tullamore, Co. Offaly, Ireland.
Nazia FaheemDepartment of Histopathology, Midland Regional Hospital Tullamore, Tullamore, Co. Offaly, Ireland.
Khalid MerghaniDepartment of Trauma and Orthopaedics, Midland Regional Hospital Tullamore, Tullamore, Co. Offaly, Ireland.
Midland Regional Hospital at Tullamore · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSchwannomas are slow-growing, benign tumours normally originating from the schwann cells of the nerve sheath. Intraosseous schwannomas account for 0.175% of primary bone tumours and are extremely rare, especially outside the axial skeleton. Monoclonal gammopathy has been associated with soft tissue schwannomas but never with the intraosseous variety. PRESENTATION OF CASE: A 55-year-old woman with a background of monoclonal gammopathy of undetermined significance (MGUS) presented with a 2-year history of right thigh pain. CT scan showed a well defined, lytic lesion with a thin peripheral rim of sclerosis in the midshaft of the femur. MRI displayed a hyperintense, well marginated and homogenous lesion. Definitive diagnosis was made based on the classical histopathological appearance of schwannoma. We managed our patient with local curettage and prophylactic cephalomedullary nailing based on her high mirel score. DISCUSSION: Intraosseous schwannomas are poorly understood but most commonly reported in middle-aged women. Radiologically, their differential diagnosis includes malignant bone tumours, solitary bone cysts, aneurysmal bone cysts and giant cell tumours. As a result, they are usually diagnosed incidentally on histology. Although malignant transformation is possible in soft tissue schwannomas, all intraosseous schwannomas reported to date have been benign.

conclusionThis case demonstrates the importance of suspecting intraosseous schwannoma as a differential diagnosis for lytic bone lesions to avoid the overtreatment of patients. We also highlight monoclonal gammopathy of undetermined significance as a potential risk factor for a poorly understood disease and make recommendations about the appropriate management of these lesions.

Indexed as

Case reportFemoral schwannomaIntraosseous schannomaMonocloncal gamopathy of underdetermined significance (MGUS)NeurilemmomaPrimary bone tumour

Identifiers

PMID32698273
PMCPMC7322230
OpenAlexW3034519588

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.