Adult-onset Still′s disease with myocarditis and hemophagocytic lymphohistiocytosis: Rare manifestation with fatal outcome

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 unkn...

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Bibliographic Details
Published in:Indian Journal of Pathology and Microbiology
Main Authors: Devika Gupta, Rajat Jagani, Satish Mendonca, Khushi Ram Rathi
Format: Article in Journal/Newspaper
Language:English
Published: Wolters Kluwer Medknow Publications 2016
Subjects:
Adult-onset Still′s disease
hemophagocytic lymphohistiocytosis
myocarditis
Pathology
RB1-214
Microbiology
QR1-502
Pink salmon
Online Access:https://doi.org/10.4103/0377-4929.174825
https://doaj.org/article/2c3cabe5ea084dc69eb17d5cdafc5cd3
Description
Summary: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.

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