AI Article Synopsis
- Cryoglobulinemia vasculitis is a potential complication to consider for patients with adult-onset Still's disease (AOSD) presenting with skin purpura.
- The case highlights the importance of including cryoglobulinemia vasculitis in the differential diagnosis when AOSD is suspected.
- This scenario adds to the understanding of the hematological complications associated with AOSD, which can include conditions like hemophagocytic syndrome and thrombotic microangiopathy.
Article Abstract
Key Clinical Message: The present case indicates that cryoglobulinemia vasculitis should be considered in the differential diagnosis of purpura in patients with adult-onset Still's disease (AOSD).
Abstract: The presence of purpura is suggested in adult-onset Still's disease (AOSD) hematological complications of hemophagocytic syndrome, disseminated intravascular coagulation, or thrombotic microangiopathy. We herein report a case of AOSD complicated by cryoglobulinemia vasculitis presenting with purpura.
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Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10918707 | PMC |
| http://dx.doi.org/10.1002/ccr3.8632 | DOI Listing |
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