| Literature DB >> 30573661 |
Claudia G Nevarez Flores1, Alexander P Sun2, Howard Hast3.
Abstract
Purpura fulminans is a rapidly progressive syndrome of intravascular thrombosis and hemorrhagic infarction of the skin. The most common infectious etiology is Neisseria meningitidis sepsis, and less commonly it has been documented as a complication of invasive Streptococcus pneumoniae In children who are otherwise healthy, splenic dysfunction is a significant predisposing factor for invasive pneumococcal infection. We present the case of a 10-month-old girl with a history of developmental delay, who developed an overwhelming infection complicated by purpura fulminans and was found to have previously undiagnosed Mowat-Wilson syndrome with anatomic asplenia. We propose screening patients with clinical features suggestive of Mowat-Wilson syndrome for asplenia to evaluate the need for additional preventive care.Entities:
Mesh:
Year: 2019 PMID: 30573661 DOI: 10.1542/peds.2018-0922
Source DB: PubMed Journal: Pediatrics ISSN: 0031-4005 Impact factor: 7.124