| Literature DB >> 32038753 |
Sabeen Yaqub1,2, Shelly A Stepenaskie1,2, Fatemeh Jafari Farshami1,2, Wilmer L Sibbitt1,2, Monthida Fangtham1,2, N Suzanne Emil1,2, Arthur D Bankhurst1,2.
Abstract
Painful, palpable purpura usually indicate underlying vasculitis. We report a case of systemic vasculitis treated with immunosuppression that developed painful, vasculitis-like purpuric lesions that progressed rapidly to fulminant Kaposi sarcoma (KS). These purpuric, tumorous lesions resolved completely following the suspension of immunosuppression; however, without immunosuppression, the underlying autoimmunity recurred. This case highlights the potential for early KS to present as a vasculitis mimic or pseudovasculitis that clinicians should keep in mind when purpuric, vasculitis-like lesions develop in an immunosuppressed patient with vasculitis. It is important to recognize these pseudovasculitis lesions as KS rather than recurrent vasculitis so that immunosuppression can be withdrawn.Entities:
Keywords: Immunosuppression; Kaposi sarcoma; purpura; vasculitis
Year: 2019 PMID: 32038753 PMCID: PMC6937164
Source DB: PubMed Journal: J Clin Aesthet Dermatol ISSN: 1941-2789