Evidence map›Paper›PMID 34584071›Full record

ReviewSpinal cord series and cases2021

Rare case of multifocal extradural and intramedullary neurosarcoidosis without pulmonary involvement: a case report and literature review.

Ryan Shields, Olivia Sagan, Logan Roebke, Josh Vander Maten, Shailen Shah, George Chang, Dalia Ibrahim, Sumayya Naz

Open access · bronzeAbstract readCase ReportsReview
In one paragraph

Review in Spinal cord series and cases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 1 institution in 1 country.

Ryan ShieldsCollege of Medicine and Life Sciences, The University of Toledo, Toledo, OH, USA. ryan.shields@rockets.utoledo.edu.ORCID 0000-0001-7177-3316
Olivia SaganCollege of Medicine and Life Sciences, The University of Toledo, Toledo, OH, USA.ORCID 0000-0001-5340-5544
Logan RoebkeCollege of Medicine and Life Sciences, The University of Toledo, Toledo, OH, USA.
Josh Vander MatenCollege of Medicine and Life Sciences, The University of Toledo, Toledo, OH, USA.
Shailen ShahCollege of Medicine and Life Sciences, The University of Toledo, Toledo, OH, USA.
George ChangDepartment of Pathology, The University of Toledo, Toledo, OH, USA.
Dalia IbrahimDepartment of Pathology, The University of Toledo, Toledo, OH, USA.
Sumayya NazDepartment of Neurology, The University of Toledo, Toledo, OH, USA.
University of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSarcoidosis is a multisystem disease characterized histologically by noncaseating granulomas. Localization of sarcoidosis to the CNS is termed neurosarcoidosis, a complex and rare neuroinflammatory form of sarcoidosis. When the spinal cord is involved, lesions are often intradural. Here, we present a rare case of progressive myelopathy secondary to multifocal spinal extradural neurosarcoidosis with spinal cord compression and without pulmonary involvement. CASE PRESENTATION: A 29-year-old African American female presented to the emergency department with numbness and paresthesia of 2-month duration in her left lower extremity and 2-week duration in her right lower extremity. The patient reported difficulty ambulating, paresthesia below the umbilicus, and back pain radiating to bilateral lower extremities. She endorsed 9-month history of cough, subjective fevers, night sweats, and unintentional 15 kg weight loss. Examination revealed 4/5 strength in the left lower extremity. MRI of the brain and spinal cord revealed enhancing extradural lesions, with spinal cord compression at T8 measuring 1.3 × 1.9 cm. Lumbar puncture demonstrated oligoclonal bands and increased CSF neutrophils, lymphocytes, monocytes, and protein. T8 laminectomy with resection of the epidural lesion was performed. Histology showed granulomas, consistent with neurosarcoidosis. At follow-up, repeat spinal MRI revealed disease progression with intramedullary involvement. Long-term immunosuppressive treatment was eventually initiated with satisfactory response. DISCUSSION: This is a rare case of myelopathy secondary to spinal extradural neurosarcoidosis. Spinal neurosarcoidosis is predominantly an intradural process. Our review of the literature identified only seven cases of extradural neurosarcoidosis presenting with compressive myelopathy. Additional insight into management and rehabilitation following pathological diagnosis is of clinical significance.

Indexed as

Central Nervous System DiseasesSarcoidosisSpinal Cord CompressionSpinal Cord DiseasesAdultFemaleHumans

Identifiers

PMID34584071
PMCPMC8477626
OpenAlexW3203461344

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.