The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature Review

<i>Background and Objectives</i>: The opsoclonus-myoclonus syndrome (OMS) is characterised by opsoclons, myoclons and impaired balance, often concomitant with sleep disorder and behavioural difficulties. The symptoms develop as a result of autoimmune response triggered by a neuroblastic...

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Main Authors: Agnieszka Mizia-Malarz, Weronika Stolpa, Grażyna Sobol-Milejska
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Medicina
Subjects:
Online Access:https://www.mdpi.com/1010-660X/56/8/412
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spelling doaj-b7e200defba74722ab2184a57fec81542020-11-25T03:26:53ZengMDPI AGMedicina1010-660X2020-08-015641241210.3390/medicina56080412The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature ReviewAgnieszka Mizia-Malarz0Weronika Stolpa1Grażyna Sobol-Milejska2Department of Pediatric Oncology, Haematology and Chemotherapy, Upper Silesia Children’s Care Heatlh Centre, Medical University of Silesia, 16 Medykow Street, 40-752 Katowice, PolandDepartment of Pediatric Oncology, Haematology and Chemotherapy, Upper Silesia Children’s Care Heatlh Centre, Medical University of Silesia, 16 Medykow Street, 40-752 Katowice, PolandDepartment of Pediatric Oncology, Haematology and Chemotherapy, Upper Silesia Children’s Care Heatlh Centre, Medical University of Silesia, 16 Medykow Street, 40-752 Katowice, Poland<i>Background and Objectives</i>: The opsoclonus-myoclonus syndrome (OMS) is characterised by opsoclons, myoclons and impaired balance, often concomitant with sleep disorder and behavioural difficulties. The symptoms develop as a result of autoimmune response triggered by a neuroblastic tumour (NT). OMS can also develop secondarily to a viral infection or as an immune response triggered by an unknown agent. This leads to the activation of B- and T-cells, which produce and release autoantibodies or cytokines directly within the central nervous system (CNS), thus damaging the neurons within the cerebellum and the brain stem. The available OMS treatments aim at decreasing lymphocyte, cytokine and autoantibody production or accelerating the utilisation of the latter. Another treatment option for OMS involves using cytostatic agents, which damage T- and B-cells causing their depletion and impaired function, which reduces their ability to produce antibodies and cytokines. <i>Materials and Methods</i>: We present a single-centre experience in treating OMS secondary to NT in 7 children. <i>Results</i>: The combined treatment with cyclophosphamide plus dexamethasone resulted in a complete resolution of OMS symptoms in 4 children, and a significant improvement in the 3 children. Two of them periodically present hyperactivity, and one girl requires an additional support at school due to special educational needs (SEN). <i>Conclusions</i>: NT resection does not resolve OMS in children with OMS secondary to NT. The combined treatment with dexamethasone plus cyclophosphamide seems to be an effective treatment of OMS.https://www.mdpi.com/1010-660X/56/8/412opsoclonus-myoclonus syndromeneuroblastic tumourstreatmentchildren
collection DOAJ
language English
format Article
sources DOAJ
author Agnieszka Mizia-Malarz
Weronika Stolpa
Grażyna Sobol-Milejska
spellingShingle Agnieszka Mizia-Malarz
Weronika Stolpa
Grażyna Sobol-Milejska
The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature Review
Medicina
opsoclonus-myoclonus syndrome
neuroblastic tumours
treatment
children
author_facet Agnieszka Mizia-Malarz
Weronika Stolpa
Grażyna Sobol-Milejska
author_sort Agnieszka Mizia-Malarz
title The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature Review
title_short The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature Review
title_full The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature Review
title_fullStr The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature Review
title_full_unstemmed The Treatment of Opsoclonus-Myoclonus Syndrome Secondary to Neuroblastic Tumours—Single-Centre Experience and Literature Review
title_sort treatment of opsoclonus-myoclonus syndrome secondary to neuroblastic tumours—single-centre experience and literature review
publisher MDPI AG
series Medicina
issn 1010-660X
publishDate 2020-08-01
description <i>Background and Objectives</i>: The opsoclonus-myoclonus syndrome (OMS) is characterised by opsoclons, myoclons and impaired balance, often concomitant with sleep disorder and behavioural difficulties. The symptoms develop as a result of autoimmune response triggered by a neuroblastic tumour (NT). OMS can also develop secondarily to a viral infection or as an immune response triggered by an unknown agent. This leads to the activation of B- and T-cells, which produce and release autoantibodies or cytokines directly within the central nervous system (CNS), thus damaging the neurons within the cerebellum and the brain stem. The available OMS treatments aim at decreasing lymphocyte, cytokine and autoantibody production or accelerating the utilisation of the latter. Another treatment option for OMS involves using cytostatic agents, which damage T- and B-cells causing their depletion and impaired function, which reduces their ability to produce antibodies and cytokines. <i>Materials and Methods</i>: We present a single-centre experience in treating OMS secondary to NT in 7 children. <i>Results</i>: The combined treatment with cyclophosphamide plus dexamethasone resulted in a complete resolution of OMS symptoms in 4 children, and a significant improvement in the 3 children. Two of them periodically present hyperactivity, and one girl requires an additional support at school due to special educational needs (SEN). <i>Conclusions</i>: NT resection does not resolve OMS in children with OMS secondary to NT. The combined treatment with dexamethasone plus cyclophosphamide seems to be an effective treatment of OMS.
topic opsoclonus-myoclonus syndrome
neuroblastic tumours
treatment
children
url https://www.mdpi.com/1010-660X/56/8/412
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