Evidence map›Paper›PMID 38094193›Full record

ArticleRadiology case reports2024

An uncommon presentation of a multifocal spinal osseous sarcoidosis: A case report on the diagnosis and exclusion with literature review.

Alex Gilman, Amanda Burke, Kailey Nolan, Lauren Beckmeyer, Donald Hefelfinger, Austin Peters, Steve Nelson

Open access · goldAbstract readCase Reports
In one paragraph

Article in Radiology case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 1 country.

Alex GilmanDepartment of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, OH, USA.
Amanda BurkeDepartment of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, OH, USA.
Kailey NolanBrethen Center for Surgical Advancement at Premier Health, Dayton, OH, USA.
Lauren BeckmeyerDepartment of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, OH, USA.
Donald HefelfingerDepartment of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, OH, USA.
Austin PetersDepartment of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, OH, USA.
Steve NelsonDepartment of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, OH, USA.
Wright State University · USPremier Health Care · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcoidosis is a granulomatous disease of indeterminate etiology. Women are more commonly affected than men at nearly twice the incidence with black women most commonly afflicted in the United States. Osseous spinal sarcoidosis (SS) is thought to be uncommon. Such lesions are often mistaken for metastatic disease, multiple myeloma, or disseminated fungal/granulomatous infection complicating the diagnosis, clinical course, and treatment. Patients presenting with clinical and imaging features of sarcoidosis may have normal serum laboratory values further complicating diagnosis. We present the case of a 61-year-old African American female with a diagnosis of osseous spinal sarcoidosis and normal calcium and ACE levels. Her initial presentation began with an incidentally discovered pulmonary nodule and was subsequently discovered to have multiple enlarging pulmonary nodules and widespread sclerotic lesions throughout her spine. This imaging presentation occurred before development of hilar adenopathy and cutaneous manifestations of sarcoidosis. Here, we describe her clinical course, exclusion of metastatic disease, and other confounders to arrive at the correct diagnosis.

Indexed as

MRINeuroradiologyNeurosarcoidosisPulmonary sarcoidosisSpinal sarcoidosis

Identifiers

PMID38094193
PMCPMC10716349
OpenAlexW4389120623

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.