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Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas

BACKGROUND: Hydatid disease is a life-threatening parasitic infestation caused by Echinococcus granulosus. Infection with E. granulosus typically results in the formation of hydatid cysts in the liver, lungs, kidney, and spleen. Primary intracranial hydatid cyst disease is extremely rare. Here, we a...

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Autores principales: Altibi, Ahmed M. A., Qarajeh, Raed A. H., Belsuzarri, Telmo A. B., Maani, Walid, Kanaan, Tareq M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154201/
https://www.ncbi.nlm.nih.gov/pubmed/27999716
http://dx.doi.org/10.4103/2152-7806.194512
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author Altibi, Ahmed M. A.
Qarajeh, Raed A. H.
Belsuzarri, Telmo A. B.
Maani, Walid
Kanaan, Tareq M. A.
author_facet Altibi, Ahmed M. A.
Qarajeh, Raed A. H.
Belsuzarri, Telmo A. B.
Maani, Walid
Kanaan, Tareq M. A.
author_sort Altibi, Ahmed M. A.
collection PubMed
description BACKGROUND: Hydatid disease is a life-threatening parasitic infestation caused by Echinococcus granulosus. Infection with E. granulosus typically results in the formation of hydatid cysts in the liver, lungs, kidney, and spleen. Primary intracranial hydatid cyst disease is extremely rare. Here, we are reporting an unusual case of Echinococcus, where the only identifiable lesion was a hydatid cyst in the brain without liver or lung involvement. We are also providing a description for the surgical technique used to remove the cyst, highlighting the possible surgical pitfalls. CASE DESCRIPTION: The patient is a 13-year-old male with a history of progressive headache for 1 month. Intracranial hydatid cyst was suspected based on computed tomography and magnetic resonance imaging findings. The cyst was delivered without rupture using hydrostatic dissection (Dowling's technique), and pathological analysis confirmed the diagnosis. Postoperatively, the patient showed marked neurological improvement and all signs and symptoms resolved. CONCLUSION: Intracranial hydatid cyst is very rare. Nevertheless, it should always be considered as a differential diagnosis in cerebral cystic lesions, especially in children. The surgical technique used to remove the cyst appears to be safe. However, several precautions must be applied intraoperatively to avoid the catastrophe of cyst rupture.
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spelling pubmed-51542012016-12-20 Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas Altibi, Ahmed M. A. Qarajeh, Raed A. H. Belsuzarri, Telmo A. B. Maani, Walid Kanaan, Tareq M. A. Surg Neurol Int Case Report BACKGROUND: Hydatid disease is a life-threatening parasitic infestation caused by Echinococcus granulosus. Infection with E. granulosus typically results in the formation of hydatid cysts in the liver, lungs, kidney, and spleen. Primary intracranial hydatid cyst disease is extremely rare. Here, we are reporting an unusual case of Echinococcus, where the only identifiable lesion was a hydatid cyst in the brain without liver or lung involvement. We are also providing a description for the surgical technique used to remove the cyst, highlighting the possible surgical pitfalls. CASE DESCRIPTION: The patient is a 13-year-old male with a history of progressive headache for 1 month. Intracranial hydatid cyst was suspected based on computed tomography and magnetic resonance imaging findings. The cyst was delivered without rupture using hydrostatic dissection (Dowling's technique), and pathological analysis confirmed the diagnosis. Postoperatively, the patient showed marked neurological improvement and all signs and symptoms resolved. CONCLUSION: Intracranial hydatid cyst is very rare. Nevertheless, it should always be considered as a differential diagnosis in cerebral cystic lesions, especially in children. The surgical technique used to remove the cyst appears to be safe. However, several precautions must be applied intraoperatively to avoid the catastrophe of cyst rupture. Medknow Publications & Media Pvt Ltd 2016-11-21 /pmc/articles/PMC5154201/ /pubmed/27999716 http://dx.doi.org/10.4103/2152-7806.194512 Text en Copyright: © 2016 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Altibi, Ahmed M. A.
Qarajeh, Raed A. H.
Belsuzarri, Telmo A. B.
Maani, Walid
Kanaan, Tareq M. A.
Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas
title Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas
title_full Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas
title_fullStr Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas
title_full_unstemmed Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas
title_short Primary cerebral echinoccocosis in a child: Case report – Surgical technique, technical pitfalls, and video atlas
title_sort primary cerebral echinoccocosis in a child: case report – surgical technique, technical pitfalls, and video atlas
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154201/
https://www.ncbi.nlm.nih.gov/pubmed/27999716
http://dx.doi.org/10.4103/2152-7806.194512
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