ArticleCureus2025
Adult-Onset Still's Disease Presenting as Aseptic Meningitis: A Case Report and Literature Review.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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.
Who cites it
2 citing papers in PubMed.
- Article
- Adult-onset Still's disease presenting with aseptic meningitis: a case report.Frontiers in immunology · 2025Article
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disease that usually presents with nonspecific symptoms, making early diagnosis difficult. It presents with high spiking fevers, salmon-colored rashes, and arthritis. However, atypical presentations of AOSD exist, as seen in this case, where AOSD manifested as aseptic meningitis, further complicating the diagnosis. Given its rarity and symptom overlap with infections and autoimmune diseases, AOSD poses significant diagnostic challenges. This is a case report of a 51-year-old Saudi Arabian female who suffered several weeks of fever and rash and was initially treated for an allergic reaction. However, the persistence of symptoms led to further investigation. A rheumatology consultation suggested AOSD based on persistent fever, leukocytosis, and negative cerebrospinal fluid cultures. Laboratory findings, including a raised ferritin level, further supported the diagnosis. She was effectively treated with corticosteroids, immunoglobulins, and other immunosuppressive drugs, resulting in complete symptom resolution. This case highlights the importance of considering AOSD in patients with aseptic meningitis and persistent systemic inflammation, reinforcing the need for timely diagnosis and intervention.
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Registered trials
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