Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report

Atypical hemolytic uremic syndrome is a rare disorder uncontrolled complement activation, which is classically manifested by anemia, thrombocytopenia and renal failure. Extrarenal manifestations are observed in 20 % of patients, most of which are associated with damage of the central nervous system....

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Main Authors: A. Yu. Smirnova, Yu. V. Dinikina, A. A. Tereshina, E. P. Evsutina, M. B. Belogurova
Format: Article
Language:Russian
Published: ABV-press 2021-04-01
Series:Онкогематология
Subjects:
Online Access:https://oncohematology.abvpress.ru/ongm/article/view/461
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author A. Yu. Smirnova
Yu. V. Dinikina
A. A. Tereshina
E. P. Evsutina
M. B. Belogurova
author_facet A. Yu. Smirnova
Yu. V. Dinikina
A. A. Tereshina
E. P. Evsutina
M. B. Belogurova
author_sort A. Yu. Smirnova
collection DOAJ
description Atypical hemolytic uremic syndrome is a rare disorder uncontrolled complement activation, which is classically manifested by anemia, thrombocytopenia and renal failure. Extrarenal manifestations are observed in 20 % of patients, most of which are associated with damage of the central nervous system. Eculizumab is effective treatment option. The article describes a case report of the severe atypical hemolytic uremic syndrome in a 20 m. o. patient who received immunotherapy with anti-GD2 antibodies (dinutuximab beta) for a high-risk neuroblastoma.
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spelling doaj.art-5a04910b85dd490eae21e8a0968b2c352023-03-30T20:15:13ZrusABV-pressОнкогематология1818-83462413-40232021-04-01161313510.17650/1818-8346-2021-16-1-31-35379Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case reportA. Yu. Smirnova0Yu. V. Dinikina1A. A. Tereshina2E. P. Evsutina3M. B. Belogurova4Almazov National Medical Research Centre, Ministry of Health of RussiaAlmazov National Medical Research Centre, Ministry of Health of RussiaAlmazov National Medical Research Centre, Ministry of Health of RussiaAlmazov National Medical Research Centre, Ministry of Health of RussiaAlmazov National Medical Research Centre, Ministry of Health of RussiaAtypical hemolytic uremic syndrome is a rare disorder uncontrolled complement activation, which is classically manifested by anemia, thrombocytopenia and renal failure. Extrarenal manifestations are observed in 20 % of patients, most of which are associated with damage of the central nervous system. Eculizumab is effective treatment option. The article describes a case report of the severe atypical hemolytic uremic syndrome in a 20 m. o. patient who received immunotherapy with anti-GD2 antibodies (dinutuximab beta) for a high-risk neuroblastoma.https://oncohematology.abvpress.ru/ongm/article/view/461atypical hemolytic uremic syndromeneuroblastomarisk factorimmunotherapy
spellingShingle A. Yu. Smirnova
Yu. V. Dinikina
A. A. Tereshina
E. P. Evsutina
M. B. Belogurova
Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report
Онкогематология
atypical hemolytic uremic syndrome
neuroblastoma
risk factor
immunotherapy
title Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report
title_full Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report
title_fullStr Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report
title_full_unstemmed Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report
title_short Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report
title_sort atypical hemolytic uremic syndrome in high risk neuroblastoma patient case report
topic atypical hemolytic uremic syndrome
neuroblastoma
risk factor
immunotherapy
url https://oncohematology.abvpress.ru/ongm/article/view/461
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AT yuvdinikina atypicalhemolyticuremicsyndromeinhighriskneuroblastomapatientcasereport
AT aatereshina atypicalhemolyticuremicsyndromeinhighriskneuroblastomapatientcasereport
AT epevsutina atypicalhemolyticuremicsyndromeinhighriskneuroblastomapatientcasereport
AT mbbelogurova atypicalhemolyticuremicsyndromeinhighriskneuroblastomapatientcasereport