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Clinical characteristics and management of neurocysticercosis patients: a retrospective assessment of case reports from Europe

  • Dominik Stelzle
  • , Annette Abraham
  • , Miriam Kaminski
  • , Veronika Schmidt
  • , Robert De Meijere
  • , Javier A. Bustos
  • , Hector Hugo Garcia
  • , Priyadarshi Soumyaranjan Sahu
  • , Branko Bobić
  • , Carmen Cretu
  • , Peter Chiodini
  • , Veronique Dermauw
  • , Brecht Devleesschauwer
  • , Pierre Dorny
  • , Ana Fonseca
  • , Sarah Gabriël
  • , Maria Ángeles Gómez Morales
  • , Minerva Laranjo-González
  • , Achim Hoerauf
  • , Ewan Hunter
  • Ronan Jambou, Maja Jurhar-Pavlova, Ingrid Reiter-Owona, Smaragda Sotiraki, Chiara Trevisan, Manuela Vilhena, Naomi F. Walker, Lorenzo Zammarchi, Andrea Sylvia Winkler
  • Technical University of Munich
  • University of Oslo
  • Charité – Universitätsmedizin Berlin
  • Instituto Nacional de Ciencias Neurológicas
  • Medical University of the Americas
  • University of Belgrade
  • Carol Davila University of Medicine and Pharmacy
  • Hospital for Tropical Diseases
  • London School of Hygiene and Tropical Medicine
  • Institute of Tropical Medicine
  • Ghent University
  • Universidade Nova de Lisboa
  • Italian National Institute of Health
  • IRTA-UAB)
  • University Hospital Bonn
  • Partner Site Bonn-Cologne
  • The Newcastle-upon-Tyne Hospitals NHS Foundation Trust
  • Institut Pasteur, Paris
  • University “Ss. Cyril and Methodius”
  • Hellenic Agricultural Organisation DIMITRA
  • Universidade de Évora
  • Liverpool School of Tropical Medicine
  • University of Florence

Producción científica: Contribución a una revistaArtículo de revisiónrevisión exhaustiva

25 Citas (Scopus)

Resumen

Objectives: Neurocysticercosis (NCC) is a parasitic disease caused by the larval stage of the tapeworm Taenia solium. NCC mainly occurs in Africa, Latin America and South-East Asia and can cause a variety of clinical signs/symptoms. Although it is a rare disease in Europe, it should nonetheless be considered as a differential diagnosis. The aim of this study was to describe clinical characteristics and management of patients with NCC diagnosed and treated in Europe. Methods: We conducted a systematic search of published and unpublished data on patients diagnosed with NCC in Europe (2000-2019) and extracted demographic, clinical and radiological information on each case, if available. Results: Out of 293 identified NCC cases, 59% of patients presented initially with epileptic seizures (21% focal onset); 52% presented with headache and 54% had other neurological signs/symptoms. The majority of patients had a travel or migration history (76%), mostly from/to Latin America (38%), Africa (32%) or Asia (30%). Treatment varied largely depending on cyst location and number. The outcome was favorable in 90% of the cases. Conclusions: Management of NCC in Europe varied considerably but often had a good outcome. Travel and migration to and from areas endemic for T. solium will likely result in continued low prevalence of NCC in Europe. Therefore, training and guidance of clinicians is recommended for optimal patient management.

Idioma originalInglés
Número de artículotaac102
PublicaciónJournal of Travel Medicine
Volumen30
N.º1
DOI
EstadoPublicada - 1 ene. 2023
Publicado de forma externa

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