1. A case of hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli after pericardiectomy
- Author
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Roeun Im, Magnus Halland, Matthew Brian Amdahl, Daniel B. Maselli, June Tome, Daniel Pfeifle, and Catherine E. Hagen
- Subjects
Adult ,medicine.medical_specialty ,Thrombotic microangiopathy ,medicine.medical_treatment ,Thrombotic thrombocytopenic purpura ,Gastroenterology ,hemic and lymphatic diseases ,Internal medicine ,medicine ,Humans ,Child ,Pericardiectomy ,Disseminated intravascular coagulation ,Purpura, Thrombotic Thrombocytopenic ,Shiga-Toxigenic Escherichia coli ,biology ,Thrombotic Microangiopathies ,business.industry ,Shiga toxin ,General Medicine ,Pseudomembranous colitis ,Microangiopathic hemolytic anemia ,medicine.disease ,Hemolysis ,Hemolytic-Uremic Syndrome ,biology.protein ,business - 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.
- Published
- 2021