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Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient

BACKGROUND: Spinal myelitis is an infrequent manifestation of spinal cord infection. It is caused by the Schistosoma species, which are endemic in South America, part of the Middle East, and Africa. CASE PRESENTATION: We report the case of a 13-year-old male adolescent complaining of progressive low...

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Autores principales: Al-Abdulwahhab, Abdulrahman Hamad, Al-Sharydah, Abdulaziz Mohammad, Al-Suhibani, Sari Saleh, Al-Jubran, Saeed Ahmad, Al-Haidey, Ali Khalaf, Al-Hifzi, Abdulkhaliq Ibrahim, Al-Issawi, Wissam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173919/
https://www.ncbi.nlm.nih.gov/pubmed/30323860
http://dx.doi.org/10.1186/s13037-018-0175-z
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author Al-Abdulwahhab, Abdulrahman Hamad
Al-Sharydah, Abdulaziz Mohammad
Al-Suhibani, Sari Saleh
Al-Jubran, Saeed Ahmad
Al-Haidey, Ali Khalaf
Al-Hifzi, Abdulkhaliq Ibrahim
Al-Issawi, Wissam
author_facet Al-Abdulwahhab, Abdulrahman Hamad
Al-Sharydah, Abdulaziz Mohammad
Al-Suhibani, Sari Saleh
Al-Jubran, Saeed Ahmad
Al-Haidey, Ali Khalaf
Al-Hifzi, Abdulkhaliq Ibrahim
Al-Issawi, Wissam
author_sort Al-Abdulwahhab, Abdulrahman Hamad
collection PubMed
description BACKGROUND: Spinal myelitis is an infrequent manifestation of spinal cord infection. It is caused by the Schistosoma species, which are endemic in South America, part of the Middle East, and Africa. CASE PRESENTATION: We report the case of a 13-year-old male adolescent complaining of progressive lower back pain and weakness of the lower extremities for 3 days. Initial magnetic resonance imaging revealed typical transverse myelitis. Subsequently, parasite serology showed a markedly elevated level of Schistosoma antibody titers, and cerebrospinal fluid analysis yielded normal results. Because of our presumptive diagnosis of neuroschistosomiasis, the patient was prescribed an empirical regimen of an anti-parasitic agent, after which his neurological deficit promptly subsided. The patient was followed for 1 year and showed a complete long-term resolution of symptoms. CONCLUSIONS: This case highlights the increasing prevalence of neuroschistosomiasis in recent years, particularly in patients with a history of travel to endemic regions. Moreover, the study reports the clinicoradiological features of this enigmatic disorder. This rare occurrence potentiates further studies to address unanswered questions about neuroschistosomiasis.
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spelling pubmed-61739192018-10-15 Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient Al-Abdulwahhab, Abdulrahman Hamad Al-Sharydah, Abdulaziz Mohammad Al-Suhibani, Sari Saleh Al-Jubran, Saeed Ahmad Al-Haidey, Ali Khalaf Al-Hifzi, Abdulkhaliq Ibrahim Al-Issawi, Wissam Patient Saf Surg Case Report BACKGROUND: Spinal myelitis is an infrequent manifestation of spinal cord infection. It is caused by the Schistosoma species, which are endemic in South America, part of the Middle East, and Africa. CASE PRESENTATION: We report the case of a 13-year-old male adolescent complaining of progressive lower back pain and weakness of the lower extremities for 3 days. Initial magnetic resonance imaging revealed typical transverse myelitis. Subsequently, parasite serology showed a markedly elevated level of Schistosoma antibody titers, and cerebrospinal fluid analysis yielded normal results. Because of our presumptive diagnosis of neuroschistosomiasis, the patient was prescribed an empirical regimen of an anti-parasitic agent, after which his neurological deficit promptly subsided. The patient was followed for 1 year and showed a complete long-term resolution of symptoms. CONCLUSIONS: This case highlights the increasing prevalence of neuroschistosomiasis in recent years, particularly in patients with a history of travel to endemic regions. Moreover, the study reports the clinicoradiological features of this enigmatic disorder. This rare occurrence potentiates further studies to address unanswered questions about neuroschistosomiasis. BioMed Central 2018-10-06 /pmc/articles/PMC6173919/ /pubmed/30323860 http://dx.doi.org/10.1186/s13037-018-0175-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Al-Abdulwahhab, Abdulrahman Hamad
Al-Sharydah, Abdulaziz Mohammad
Al-Suhibani, Sari Saleh
Al-Jubran, Saeed Ahmad
Al-Haidey, Ali Khalaf
Al-Hifzi, Abdulkhaliq Ibrahim
Al-Issawi, Wissam
Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient
title Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient
title_full Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient
title_fullStr Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient
title_full_unstemmed Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient
title_short Neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient
title_sort neuroschistosomiasis mimicking lower back pain: case report of a rare differential diagnosis in a pediatric patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173919/
https://www.ncbi.nlm.nih.gov/pubmed/30323860
http://dx.doi.org/10.1186/s13037-018-0175-z
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