| Literature DB >> 33527058 |
Muhammad Hafiz Kamarul Bahrin1, Harini Vijayenthiran2, Laura Stimson2, Humayun Ahmad2.
Abstract
Immune thrombocytopenia purpura (ITP) involves autoimmune induced platelet destruction and decreased platelet production in part due to autoantibody destruction mechanisms. Most autoantibodies involved in its pathogenesis invoke autoreactive T cells and cytokine imbalance, and most drug therapies target these mechanisms. We describe a man in his late 40s, with a medical history of ITP, who presented with blood blisters on his mucosal surfaces and bruises on all four limbs with petechial rashes. He subsequently developed epistaxis and hemoptysis. In the recent past, he had been camping in Malta and felt feverish and nauseous on return. This was his first relapse of the disease in six years, and was unresponsive to prednisolone, IV immunoglobulins, and methylprednisolone, subsequently requiring romiplostim to recover platelet counts and reduce bleeding. When investigating the underlying causes of thrombocytopenia, aspects of virology and rickettsial serology were positive, requiring precautionary measures with long-term maintenance immunosuppression to prevent reactivation of infection.Entities:
Keywords: haemorrhagic bullae; immune thrombocytopenia purpura; romiplostim
Year: 2020 PMID: 33527058 PMCID: PMC7845478 DOI: 10.7759/cureus.12377
Source DB: PubMed Journal: Cureus ISSN: 2168-8184