| Literature DB >> 30061130 |
Allison Virginia Lange1, Salahuddin Kazi1, Weina Chen2, Arti Barnes3.
Abstract
We describe a case of an adult with dermatomyositis (DM) who presents with a rash, high fevers, tachycardia and hypotension, initially concerning for an infectious aetiology or a DM flare. She was found to have cytomegalovirus viraemia which improved after starting valganciclovir. After extensive workup and lack of improvement with broad-spectrum antimicrobial therapy, intravenous immunoglobulin and steroids, the patient was diagnosed with macrophage activation syndrome after bone marrow biopsy and levels of soluble CD25 (soluble interleukin (IL)-2 receptor) and IL2 were obtained. Unfortunately, despite therapy with dexamethasone, anakinra and etoposide, the patient decompensated and the patient's family opted for comfort care. The patient subsequently expired in the intensive care unit. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: adult intensive care; connective tissue disease; infectious diseases
Mesh:
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Year: 2018 PMID: 30061130 DOI: 10.1136/bcr-2018-225231
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X