From Cough to Myocarditis: A Systemic Tale of Adult-Onset Still's Disease
Iman A. A Shaat, Faiza Javed, Taha Elsahy, Praveenraja Shanmugam, Rabbiya Shafqat Cheema

TL;DR
This paper presents a case of a rare inflammatory disease, Adult-Onset Still's Disease, highlighting its diagnostic challenges and successful treatment with corticosteroids.
Contribution
The paper contributes a detailed case report emphasizing the diagnostic and therapeutic importance of recognizing AOSD through elevated ferritin and systemic features.
Findings
AOSD was diagnosed based on prolonged fever, hyperferritinemia, and exclusion of other conditions.
The patient showed rapid improvement with high-dose corticosteroids.
Systemic features like myocarditis and splenomegaly indicated severe disease.
Abstract
Adult-onset Still's disease (AOSD) is a rare systemic autoinflammatory disorder that presents a significant diagnostic challenge due to its nonspecific features and overlap with infectious, autoimmune, and malignant conditions. We report a case of a 39-year-old man who initially presented with fever, sore throat, myalgia, and cough. He was initially treated for a presumed respiratory infection. On re-presentation, he developed worsening pyrexia, polyarthritis, odynophagia, and dyspnea. Laboratory investigations revealed markedly elevated inflammatory markers, hyperferritinemia exceeding 6000 µg/L, neutrophilic leukocytosis, anemia, thrombocytopenia, and deranged liver function tests. Imaging demonstrated splenomegaly and pleural effusion, while elevated troponin and ECG changes were consistent with myocarditis. Extensive infectious, autoimmune, and malignant evaluations were…
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Taxonomy
TopicsAutoimmune and Inflammatory Disorders Research · Eosinophilic Disorders and Syndromes
