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Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas

Multiple intracranial cavernomas are rare and occur mostly in familial cases. Clinical presentation with simultaneous rupture of two or more lesions has only been reported in four cases to date. A 15-year-old boy presented with simultaneous right frontal and superior vermian hematomas with hydroceph...

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Autores principales: Tyagi, Gaurav, Sikaria, Abhay, Birua, Gyani Jail Singh, Beniwal, Manish, Srinivas, Dwarakanath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Cerebrovascular Surgeons and Korean NeuroEndovascular Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537648/
https://www.ncbi.nlm.nih.gov/pubmed/35220696
http://dx.doi.org/10.7461/jcen.2022.E2021.08.001
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author Tyagi, Gaurav
Sikaria, Abhay
Birua, Gyani Jail Singh
Beniwal, Manish
Srinivas, Dwarakanath
author_facet Tyagi, Gaurav
Sikaria, Abhay
Birua, Gyani Jail Singh
Beniwal, Manish
Srinivas, Dwarakanath
author_sort Tyagi, Gaurav
collection PubMed
description Multiple intracranial cavernomas are rare and occur mostly in familial cases. Clinical presentation with simultaneous rupture of two or more lesions has only been reported in four cases to date. A 15-year-old boy presented with simultaneous right frontal and superior vermian hematomas with hydrocephalus. The patient underwent a ventriculoperitoneal shunt, and his magnetic resonance imaging (MRI) revealed multiple cavernomas with bleed in the above-mentioned locations. The patient underwent a midline suboccipital craniotomy and excision of the cavernoma. The supratentorial lesions were left in situ in lieu of small size, no history of seizures, mass effect, or other neurological deficits. The patient recovered well from surgery with significant improvement in truncal ataxia. He remained asymptomatic for supratentorial lesions at follow-up. Cavernomas should be considered as differential diagnoses in cases of multiple intraparenchymal hemorrhages, especially in pediatric patients. The surgical management should be rationalized based on the lesion location, the eloquence of the surrounding parenchyma, mass effect, and the risks of re-rupture. Due to the rarity of multiple simultaneous hemorrhages, the management of multiple cavernomas remains controversial. The patient’s relatives can be screened with MRI to rule out the familial form of the disease. Strict clinical and radiological follow-up is a must in such patients.
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spelling pubmed-95376482022-10-17 Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas Tyagi, Gaurav Sikaria, Abhay Birua, Gyani Jail Singh Beniwal, Manish Srinivas, Dwarakanath J Cerebrovasc Endovasc Neurosurg Case Report Multiple intracranial cavernomas are rare and occur mostly in familial cases. Clinical presentation with simultaneous rupture of two or more lesions has only been reported in four cases to date. A 15-year-old boy presented with simultaneous right frontal and superior vermian hematomas with hydrocephalus. The patient underwent a ventriculoperitoneal shunt, and his magnetic resonance imaging (MRI) revealed multiple cavernomas with bleed in the above-mentioned locations. The patient underwent a midline suboccipital craniotomy and excision of the cavernoma. The supratentorial lesions were left in situ in lieu of small size, no history of seizures, mass effect, or other neurological deficits. The patient recovered well from surgery with significant improvement in truncal ataxia. He remained asymptomatic for supratentorial lesions at follow-up. Cavernomas should be considered as differential diagnoses in cases of multiple intraparenchymal hemorrhages, especially in pediatric patients. The surgical management should be rationalized based on the lesion location, the eloquence of the surrounding parenchyma, mass effect, and the risks of re-rupture. Due to the rarity of multiple simultaneous hemorrhages, the management of multiple cavernomas remains controversial. The patient’s relatives can be screened with MRI to rule out the familial form of the disease. Strict clinical and radiological follow-up is a must in such patients. Korean Society of Cerebrovascular Surgeons and Korean NeuroEndovascular Society 2022-09 2022-02-28 /pmc/articles/PMC9537648/ /pubmed/35220696 http://dx.doi.org/10.7461/jcen.2022.E2021.08.001 Text en Copyright © 2022 by KSCVS and KoNES https://creativecommons.org/licenses/by-nc/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tyagi, Gaurav
Sikaria, Abhay
Birua, Gyani Jail Singh
Beniwal, Manish
Srinivas, Dwarakanath
Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas
title Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas
title_full Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas
title_fullStr Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas
title_full_unstemmed Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas
title_short Surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas
title_sort surgical management of simultaneous supra- and infratentorial hemorrhages in a pediatric patient with multiple cavernomas
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537648/
https://www.ncbi.nlm.nih.gov/pubmed/35220696
http://dx.doi.org/10.7461/jcen.2022.E2021.08.001
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