| Literature DB >> 34677733 |
June Tome1, Daniel Barry Maselli2, Roeun Im3, Matthew Brian Amdahl1, Daniel Pfeifle1, Catherine Hagen3, Magnus Halland4.
Abstract
The majority of cases of Shiga toxin-producing Escherichia coli are self-limited; however, the infection can occasionally be complicated by more severe phenomena, such as thrombotic microangiopathy, with resultant end-organ damage to the kidneys, colon, nervous system, and various other tissues. Shiga toxin-induced hemolytic uremic syndrome (ST-HUS)-the constellation of thrombocytopenia, hemolysis, and renal failure resulting from thrombotic microangiopathy in a subset of infections producing the Shiga toxin-is classically observed in the pediatric population. Nevertheless, the diagnosis should be considered in adults with this presentation, and especially in those with colonic findings suggestive of ischemia. ST-HUS must also be distinguished from other thrombotic microangiopathies and related conditions, such as disseminated intravascular coagulation, thrombotic thrombocytopenic purpura, and complement-mediated HUS, as these diagnoses prompt alternate management strategies. Here, we present a case of ST-HUS in a gentleman following pericardiectomy who was infected with non-O157:H7 E. coli producing Shiga toxin 2.Entities:
Keywords: Microangiopathic hemolytic anemia; Pseudomembranous colitis; Shiga toxin-producing Escherichia coli
Mesh:
Year: 2021 PMID: 34677733 DOI: 10.1007/s12328-021-01539-8
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265