Publication Type : Journal Article
Publisher : Medknow
Source : Indian Journal of Pathology and Microbiology
Url : https://doi.org/10.4103/0377-4929.174825
Campus : Faridabad
School : School of Medicine
Year : 2016
Abstract : Adult-onset Still's disease (AOSD) is a rare inflammatory disorder of unknown etiology characterized by fever, evanescent pink salmon rash, arthritis, and multiorgan involvement. Here, we report an unusual manifestation of AOSD in a 40-year-old male who presented to our hospital with pyrexia of unknown origin and rash of 3 weeks duration. All his serological investigations and imaging studies were unremarkable. He was fulfilling clinical and laboratory criteria as per Yamaguchi for AOSD and was managed for the same. Our patient did not respond well to the treatment, had a downhill course, and succumbed to his illness. Autopsy confirmed myocarditis and florid bone marrow reactive hemophagocytosis as the cause of his death.
Cite this Research Publication : Devika Gupta, Rajat Jagani, Satish Mendonca, KhushiRam Rathi, Adult-onset Still′s disease with myocarditis and hemophagocytic lymphohistiocytosis: Rare manifestation with fatal outcome, Indian Journal of Pathology and Microbiology, Medknow, 2016, https://doi.org/10.4103/0377-4929.174825