Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4046
Title: Pediatric neuroschistosomiasis: A case report and review of the literature
Authors: Wen, S. C. H.
Kumbla, S.
Ryan, M. M.
Anderson, R.
Steer, A.
Wray, A.
Issue Date: 2019
Source: 8, (5), 2019, p. 489-491
Pages: 489-491
Journal: Journal of the Pediatric Infectious Diseases Society
Abstract: Neuroschistosomiasis is a rare but severe manifestation of Schistosoma infection. Diagnosis is challenging and surgical biopsy is often required to confirm diagnosis and exclude malignancy. We present a pediatric case of presumed pseudotumoral cerebral schistosomiasis secondary to Schistosoma mansoni with an excellent therapeutic response to empirical praziquantel and corticosteroid treatment.L6298261062019-11-18
2019-11-25
DOI: 10.1093/jpids/piz009
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L629826106&from=exporthttp://dx.doi.org/10.1093/jpids/piz009 |
Keywords: child;clinical article;contrast enhancement;corticosteroid therapy;electrolyte blood level;eosinophilia;female;headache;human;neuroschistosomiasis;nuclear magnetic resonance imaging;levetiracetam;priority journal;review;Schistosoma mansoni;school child;seizure;serology;temporal lobe;dexamethasoneelectrolyte;olfactory hallucination;praziquantel;basal ganglion;case report
Type: Article
Appears in Sites:Children's Health Queensland Publications

Show full item record

Page view(s)

46
checked on Mar 20, 2025

Google ScholarTM

Check

Altmetric


Items in DORA are protected by copyright, with all rights reserved, unless otherwise indicated.