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1.
Emerg Infect Dis ; 27(5): 1509-1512, 2021 05.
Artículo en Inglés | MEDLINE | ID: mdl-33900194

RESUMEN

We report a fatal case of hemolytic uremic syndrome with urinary tract infection in Japan caused by Shiga toxin-producing Escherichia coli. We genotypically identified the isolate as OX18:H2. Whole-genome sequencing revealed 3 potentially pathogenic lineages (OX18:H2, H19, and H34) that have been continuously isolated in Japan.


Asunto(s)
Infecciones por Escherichia coli , Síndrome Hemolítico-Urémico , Escherichia coli Shiga-Toxigénica , Humanos , Japón , Escherichia coli Shiga-Toxigénica/genética , Secuenciación Completa del Genoma
2.
Nephrology (Carlton) ; 23(6): 592-596, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28976051

RESUMEN

Children with systemic lupus erythematosus (SLE) generally undergo a pretreatment kidney biopsy. However, some of these patients, especially those with antiphospholipid syndrome (APS), may experience serious coagulopathic complications. We report herein two cases of paediatric SLE with APS in which, despite normal blood test results, the disparate coagulopathic complications of haemorrhage and embolism developed following a kidney biopsy. Case 1 was, an 8-year-old male in whom, primary APS was initially diagnosed. Fourteen months later SLE was diagnosed. Based on a percutaneous kidney biopsy, International Society of Nephrology and the Renal Pathology Society (ISN/RPS) class III-A lupus nephritis was histologically diagnosed. On post-biopsy Day 9, a giant haematoma in the fascia of the left kidney developed and was accompanied by changes in the vital signs. Case 2, a 13-year-old male, initially received the diagnosis of SLE with APS and underwent two courses of pulse methylprednisolone therapy. His coagulation abnormalities improved, and a percutaneous needle kidney biopsy was performed, leading to the histological diagnosis of ISN/RPS class III-A lupus nephritis. Furthermore, thrombotic microangiopathy was also detected in the renal histopathology. On post biopsy Day 6, the patient experienced right leg pain. A contrast CT and lower extremity ultrasonography detected a massive deep vein thrombosis and partial left pulmonary artery thrombosis. A kidney biopsy in children with SLE and APS can cause lethal coagulopathic complications, and the risks to such patients should be weighed carefully before the procedure is performed.


Asunto(s)
Síndrome Antifosfolípido/complicaciones , Arteriopatías Oclusivas/etiología , Biopsia/efectos adversos , Hematoma/etiología , Riñón/patología , Lupus Eritematoso Sistémico/complicaciones , Nefritis Lúpica/etiología , Trombosis de la Vena/etiología , Adolescente , Edad de Inicio , Anticoagulantes/uso terapéutico , Síndrome Antifosfolípido/sangre , Síndrome Antifosfolípido/diagnóstico , Síndrome Antifosfolípido/tratamiento farmacológico , Arteriopatías Oclusivas/sangre , Arteriopatías Oclusivas/diagnóstico , Arteriopatías Oclusivas/tratamiento farmacológico , Coagulación Sanguínea , Niño , Glucocorticoides/uso terapéutico , Hematoma/sangre , Hematoma/diagnóstico , Hematoma/tratamiento farmacológico , Humanos , Lupus Eritematoso Sistémico/diagnóstico , Lupus Eritematoso Sistémico/tratamiento farmacológico , Nefritis Lúpica/patología , Masculino , Factores de Riesgo , Tomografía Computarizada por Rayos X , Ultrasonografía Doppler en Color , Trombosis de la Vena/sangre , Trombosis de la Vena/diagnóstico , Trombosis de la Vena/tratamiento farmacológico
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