The medical therapy for cerebellar mutism syndrome: a case report and literature review.


Journal

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
ISSN: 1433-0350
Titre abrégé: Childs Nerv Syst
Pays: Germany
ID NLM: 8503227

Informations de publication

Date de publication:
09 2021
Historique:
received: 29 03 2021
accepted: 26 05 2021
pubmed: 16 6 2021
medline: 16 9 2021
entrez: 15 6 2021
Statut: ppublish

Résumé

Cerebellar mutism syndrome (CMS) represents a major complication affecting many children that undergo surgery for posterior fossa lesions. Etiology and pathophysiology are still not fully understood. CMS deeply influences quality of life and recovery of these patients. An effective treatment has not been defined yet. This case-based review aims at analyzing the available evidence and knowledge to better delineate this phenomenon and to determine whether CMS can be successfully treated with pharmacological therapy. Systematic research and retrieval of databases were conducted analyzing all papers where medical treatment of CMS was reported. A summary of the latest understanding and reports regarding definition, clinical manifestations, pathophysiology, management, and outcome of CMS has been conducted. Consensus on definition of this syndrome is lacking. CMS is the term accepted by the Posterior Fossa Society in 2016. Pathophysiology is still poorly understood but the most likely mechanism is injury along proximal components of the efferent cerebellar pathway. Nine papers describing positive effects of pharmacological therapy for CMS have been identified. Fluoxetine, zolpidem, bromocriptine, and midazolam are the drugs that seem to alleviate symptoms of CMS and improve recovery. To date, cognitive rehabilitation and physiotherapy are the only treatment options available. CMS has deep impact on affected children and their families. Despite attempts to identify preventive measures and treatment, cases still occur on a regular basis. Pharmacological treatments have been proposed to help reduce the symptoms of CMS with some promising results, but reports are limited; therefore, further studies are needed.

Identifiants

pubmed: 34128119
doi: 10.1007/s00381-021-05233-5
pii: 10.1007/s00381-021-05233-5
doi:

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2727-2734

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Alice Noris (A)

Neurosurgery and Functional Neurosurgery Unit, Department of Neurosciences, Meyer Children's Hospital Florence, Viale Gaetano Pieraccini, 24, 50139, Florence, Italy.

Anna Zicca (A)

Department of Anesthesia and Intensive Care, Meyer Children's Hospital, Florence, Italy.

Matteo Lenge (M)

Neurosurgery and Functional Neurosurgery Unit, Department of Neurosciences, Meyer Children's Hospital Florence, Viale Gaetano Pieraccini, 24, 50139, Florence, Italy.

Edoardo Picetti (E)

Department of Anesthesia and Intensive Care, Parma University Hospital, Parma, Italy.

Clelia Zanaboni (C)

Department of Anesthesia and Intensive Care, Parma University Hospital, Parma, Italy.

Sandra Rossi (S)

Department of Anesthesia and Intensive Care, Parma University Hospital, Parma, Italy.

Flavio Giordano (F)

Neurosurgery and Functional Neurosurgery Unit, Department of Neurosciences, Meyer Children's Hospital Florence, Viale Gaetano Pieraccini, 24, 50139, Florence, Italy. flavio.giordano@meyer.it.

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