Evidence map›Paper›PMID 39385309›Full record

ReviewJournal of medical case reports2024

Adult-onset Still's disease masquerading as acute coronary syndrome: a case report and review of the literature.

Indigo Milne, Rhea Kanwar, Whitney Martin, Daniel Egert, Allison Leisgang, Shirley A Albano-Aluquin, Maria P Henao, Christine Kreider, Paddy Ssentongo

Abstract readCase ReportsReview
In one paragraph

Review in Journal of medical case reports, 2024. 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
–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

2 citing papers in PubMed.

  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

9 authors.

Indigo MilnePenn State College of Medicine, Hershey, PA, USA.
Rhea KanwarPenn State College of Medicine, Hershey, PA, USA.
Whitney MartinDivision of Rheumatology, Department of Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.
Daniel EgertDivision of Hematology and Oncology, Department of Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.
Allison LeisgangDepartment of Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.
Shirley A Albano-AluquinDivision of Rheumatology, Department of Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.
Maria P HenaoDivision of Allergy and Immunology, Department of Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.
Christine KreiderDepartment of Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.
Paddy SsentongoDivision of Infectious Diseases and Epidemiology, Department of Medicine, Penn State Health Milton S. Hershey Medical Center, 500 University Drive, Hershey, PA, 17033, USA. pssentongo@pennstatehealth.psu.edu.ORCID http://orcid.org/0000-0003-1565-5731

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAdult-onset Still's disease is a rare systemic autoinflammatory disease. We present a case of a young man with a constellation of symptoms and myopericarditis as a complication of this disease. CASE: A 36-year-old Hispanic man with no significant past medical history developed a quotidian fever pattern following an upper respiratory tract infection. He initially presented with chest pain concerning for myocardial infarction and underwent cardiac catheterization, which revealed non-obstructive coronary artery disease. He was found to have myopericarditis, significant neutrophilic leukocytosis, and hyperferritinemia. He improved on high-dose corticosteroids but developed steroid-induced psychosis, and 4 months from symptom onset, he finally received tocilizumab, which eventually induced remission without adverse reactions. DISCUSSION: Adult-onset Still's disease should be considered in a patient with fevers of undetermined origin. Due to its multisystemic involvement, adult-onset Still's disease is often a diagnosis arrived at after an extensive cardiac, hematologic, malignant, and infectious workup. Imaging, laboratory testing, and bone marrow biopsy were necessary to rule out alternative etiologies of this patient's presentation. Steroids are the mainstay of treatment because they are easily affordable, although the high risk of adverse effects makes them less desirable. Interleukin-1 inhibitors (anakinra or canakinumab) and interleukin-6 inhibitor tocilizumab are the steroid-sparing biologic agents of choice but are cost-prohibitive.

conclusionAdult-onset Still's disease should be considered in the differential diagnoses of fever of undetermined origin. Early identification and initiation of treatment are critical to faster recovery and prevention of progression to severe complications. Steroids remain the standard first-line therapy and should be followed by disease-modifying steroid sparing drugs. The social determinants of health may preclude their timely initiation and should alert providers of proactive ways to avoid further delays.

Indexed as

Acute Coronary SyndromeAntibodies, Monoclonal, HumanizedStill's Disease, Adult-OnsetAdultDiagnosis, DifferentialFever of Unknown OriginHumansMaleMyocarditisPericarditisAntibodies, Monoclonal, HumanizedtocilizumabAdult-onset Still’s diseaseBone marrow biopsyFever of unknown originHemophagocytic lymphohistiocytosis

Identifiers

PMID39385309
PMCPMC11465706

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Registered trials

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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.