Abstract

Background. Acute intestinal infections (AII) caused by Shiga-like toxin-producing Escherichia coli and accompanied by hemolytic uremic syndrome (HUS) development are characterized by rapid progression and poor prognosis. Bloody diarrhea (hemorrhagic colitis) requires timely medical treatment both at young age and at adolescence. The severe course of HUS affected by AII caused by enterohaemorrhagic Escherichia coli requires additional medical attention and timely renal replacement therapy (hemodialysis). Clinical Case Description. The description and analysis of the severe course of HUS affected by AII in 14 years old adolescent girl is presented. There were some difficulties during diagnostics and thus the pathogenetic therapy onset was delayed. Differential diagnosis between typical and atypical HUS was performed. The disease was characterized by rapid progression of acute kidney injury, cerebrovascular disease and ischemia, multiple organ dysfunction syndrome and disseminated intravascular coagulation resulting in fatal case. Conclusion. Atypical HUS is the most frequent cause of multiple organ dysfunction syndrome alongside with acute kidney injury. The challenges of early diagnostics of atypical GUS in childhood are not fully solved nowadays and require additional attention of pediatricians. The clinical case of atypical GUS complicated by intestinal infection caused by enterohaemorrhagic Escherichia coli is described in this article. The severity of the disease course was due to the early manifestation of extrarenal symptoms and multiple organ failure.

Highlights

  • Acute intestinal infections (AII) caused by Shiga-like toxin-producing Escherichia coli and accompanied by hemolytic uremic syndrome (HUS) development are characterized by rapid progression and poor prognosis

  • The severe course of HUS affected by AII caused by enterohaemorrhagic Escherichia coli requires additional medical attention and timely renal replacement therapy

  • The description and analysis of the severe course of HUS affected by AII in 14 years old adolescent girl is presented

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Summary

Клиническое наблюдение

Университет), Москва, Российская Федерация 2 Детская городская клиническая больница No 9 им. ОБОСНОВАНИЕ Гемолитико-уремический синдром (ГУС) — острое заболевание с триадой симптомов: Кумбс-негативной гемолитической анемией с фрагментированными эритроцитами (шизоцитами), тромбоцитопенией и острой почечной недостаточностью [1]. В основе патогенеза заболевания лежит повреждение эндотелия артериальных сосудов шига-токсином с развитием распространенной окклюзии тромбами сосудов мелкого калибра, прежде всего сосудов почек, с развитием острой почечной недостаточности [1, 6, 7]. Течение STEC-ГУС, как правило, тяжелое, с развитием экстраренальных симптомов и полиорганной недостаточности в период развития заболевания [7]. Кишечная инфекция и диарея могут спровоцировать первичный эпизод атипичного ГУС, что иногда затрудняет дифференциальную диагностику с типичным вариантом заболевания. Challenges in Diagnostics and Management of Atypical Hemolytic Uremic Syndrome Associated with Acute Intestinal Infection in Adolescent: Clinical Case

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