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A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report

INTRODUCTION AND IMPORTANCE: Neurocysticercosis (NCC) is the most common helminthic central nervous system infection (CNS) in the Western hemisphere and the most common cause of acquired epilepsy worldwide. Due to its relatively prolonged latent period and clinical similarity to other infectious dis...

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Autores principales: Welch, Rachel L., Bernardin, Brooke, Albayar, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411572/
https://www.ncbi.nlm.nih.gov/pubmed/35987027
http://dx.doi.org/10.1016/j.ijscr.2022.107477
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author Welch, Rachel L.
Bernardin, Brooke
Albayar, Ahmed
author_facet Welch, Rachel L.
Bernardin, Brooke
Albayar, Ahmed
author_sort Welch, Rachel L.
collection PubMed
description INTRODUCTION AND IMPORTANCE: Neurocysticercosis (NCC) is the most common helminthic central nervous system infection (CNS) in the Western hemisphere and the most common cause of acquired epilepsy worldwide. Due to its relatively prolonged latent period and clinical similarity to other infectious diseases – including bacterial or viral meningitis and other helminthic infections – NCC may be difficult to diagnose, especially for clinicians who rarely encounter it. CASE PRESENTATION: This case report discusses a patient with obstructive hydrocephalus and eosinophilic meningitis secondary to racemose NCC. The diagnosis process was initially complicated by the patient's history of pork allergy and absence of radiographic evidence of helminthic CNS infection. Further investigation showed a 4th ventricle multi-cystic lesion causing hydrocephalus which prompted a surgical intervention with a ventriculoperitoneal shunt (VPS) in conjunction with anti-helminthic medical treatment. At 1-year follow-up, the patient has reported recurrence of VPS related complications. CLINICAL DISCUSSION: Larval cysts typically deposit within the brain parenchyma, making them easily detected on head computed tomography (CT) scans and leading to neurologic sequelae such as epilepsy. In this case, the absence of CT evidence of NCC and the patient's lifelong history of pork allergy slowed the diagnosis process. CONCLUSION: Racemose NCC is a rare subset of the disease in which cyst clusters occupy the extra parenchymal space, thereby changing the symptomatic profile and making the cysts more difficult to visualize in imaging studies. In this case, magnetic resonance imaging (MRI) was the best imaging modality to diagnosis extra parenchymal NCC and guide its surgical management.
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spelling pubmed-94115722022-08-27 A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report Welch, Rachel L. Bernardin, Brooke Albayar, Ahmed Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Neurocysticercosis (NCC) is the most common helminthic central nervous system infection (CNS) in the Western hemisphere and the most common cause of acquired epilepsy worldwide. Due to its relatively prolonged latent period and clinical similarity to other infectious diseases – including bacterial or viral meningitis and other helminthic infections – NCC may be difficult to diagnose, especially for clinicians who rarely encounter it. CASE PRESENTATION: This case report discusses a patient with obstructive hydrocephalus and eosinophilic meningitis secondary to racemose NCC. The diagnosis process was initially complicated by the patient's history of pork allergy and absence of radiographic evidence of helminthic CNS infection. Further investigation showed a 4th ventricle multi-cystic lesion causing hydrocephalus which prompted a surgical intervention with a ventriculoperitoneal shunt (VPS) in conjunction with anti-helminthic medical treatment. At 1-year follow-up, the patient has reported recurrence of VPS related complications. CLINICAL DISCUSSION: Larval cysts typically deposit within the brain parenchyma, making them easily detected on head computed tomography (CT) scans and leading to neurologic sequelae such as epilepsy. In this case, the absence of CT evidence of NCC and the patient's lifelong history of pork allergy slowed the diagnosis process. CONCLUSION: Racemose NCC is a rare subset of the disease in which cyst clusters occupy the extra parenchymal space, thereby changing the symptomatic profile and making the cysts more difficult to visualize in imaging studies. In this case, magnetic resonance imaging (MRI) was the best imaging modality to diagnosis extra parenchymal NCC and guide its surgical management. Elsevier 2022-08-05 /pmc/articles/PMC9411572/ /pubmed/35987027 http://dx.doi.org/10.1016/j.ijscr.2022.107477 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Welch, Rachel L.
Bernardin, Brooke
Albayar, Ahmed
A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report
title A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report
title_full A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report
title_fullStr A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report
title_full_unstemmed A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report
title_short A hidden infection: Racemose neurocysticercosis causing hydrocephalus; a case report
title_sort hidden infection: racemose neurocysticercosis causing hydrocephalus; a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411572/
https://www.ncbi.nlm.nih.gov/pubmed/35987027
http://dx.doi.org/10.1016/j.ijscr.2022.107477
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