Giant cerebellar cavernous malformation in children: A case report and literature review

Giant cerebellar cavernomas in children are rare and must be differentiated from hemorrhagic cerebellar tumors. The diagnosis and treatment of giant cerebellar cavernomas is challenging, but complete surgical resection can lead to favorable outcomes and complete neurological recovery in most cases....

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Published in:	Journal of cerebrovascular and endovascular neurosurgery Vol. 26; no. 3; pp. 304 - 310
Main Authors:	Akramov, Olim Zaribovich, Nazarova, Lilia Aleksandrovna, Kurbanov, Fuat Mukadasavoch, Tashmatov, Sukhrob Abdurashibovich, Rakhimov, Ikrom Ismatovich, Usmankhanov, Odilkhon Ayubxanovich, Chaurasia, Bipin
Format:	Journal Article
Language:	English
Published:	Korea (South) Korean Society of Cerebrovascular Surgeons and Korean NeuroEndovascular Society 01-09-2024 대한뇌혈관외과학회
Subjects:	Case Report 신경외과학 Central nervous system vascular malformations Cerebellum Cerebral cavernous malformation
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Abstract	Giant cerebellar cavernomas in children are rare and must be differentiated from hemorrhagic cerebellar tumors. The diagnosis and treatment of giant cerebellar cavernomas is challenging, but complete surgical resection can lead to favorable outcomes and complete neurological recovery in most cases. We present a case of eight months old baby who was diagnosed with a giant cavernoma resulting in secondary obstructive hydrocephalus with neuropsychiatric presentations. The patient underwent a paramedian craniotomy surgery with a suboccipital approach and complete surgical resection of the cavernoma was done. Over nine months of observation, the child showed improvement in their ability to walk and fully recovered from a neurological perspective. We also conducted a literature review to identify eleven cases of giant cerebellar cavernomas in children, including our case. The data were analyzed to determine the clinical features, treatment, and outcomes of giant cerebellar cavernomas in children.
AbstractList	Giant cerebellar cavernomas in children are rare and must be differentiated from hemorrhagic cerebellar tumors. The diagnosis and treatment of giant cerebellar cavernomas is challenging, but complete surgical resection can lead to favorable outcomes and complete neurological recovery in most cases. We present a case of eight months old baby who was diagnosed with a giant cavernoma resulting in secondary obstructive hydrocephalus with neuropsychiatric presentations. The patient underwent a paramedian craniotomy surgery with a suboccipital approach and complete surgical resection of the cavernoma was done. Over nine months of observation, the child showed improvement in their ability to walk and fully recovered from a neurological perspective. We also conducted a literature review to identify eleven cases of giant cerebellar cavernomas in children, including our case. The data were analyzed to determine the clinical features, treatment, and outcomes of giant cerebellar cavernomas in children. Giant cerebellar cavernomas in children are rare and must be differentiated from hemorrhagic cerebellar tumors. The diagnosis and treatment of giant cerebellar cavernomas is challenging, but complete surgical resection can lead to favorable outcomes and complete neurological recovery in most cases. We present a case of eight months old baby who was diagnosed with a giant cavernoma resulting in secondary obstructive hydrocephalus with neuropsychiatric presentations. The patient underwent a paramedian craniotomy surgery with a suboccipital approach and complete surgical resection of the cavernoma was done. Over nine months of observation, the child showed improvement in their ability to walk and fully recovered from a neurological perspective. We also conducted a literature review to identify eleven cases of giant cerebellar cavernomas in children, including our case. The data were analyzed to determine the clinical features, treatment, and outcomes of giant cerebellar cavernomas in children. KCI Citation Count: 0 Giant cerebellar cavernomas in children are rare and must be differentiated from hemorrhagic cerebellar tumors. The diagnosis and treatment of giant cerebellar cavernomas is challenging, but complete surgical resection can lead to favorable outcomes and complete neurological recovery in most cases. We present a case of eight months old baby who was diagnosed with a giant cavernoma resulting in secondary obstructive hydrocephalus with neuropsychiatric presentations. The patient underwent a paramedian craniotomy surgery with a suboccipital approach and complete surgical resection of the cavernoma was done. Over nine months of observation, the child showed improvement in their ability to walk and fully recovered from a neurological perspective. We also conducted a literature review to identify eleven cases of giant cerebellar cavernomas in children, including our case. The data were analyzed to determine the clinical features, treatment, and outcomes of giant cerebellar cavernomas in children.Giant cerebellar cavernomas in children are rare and must be differentiated from hemorrhagic cerebellar tumors. The diagnosis and treatment of giant cerebellar cavernomas is challenging, but complete surgical resection can lead to favorable outcomes and complete neurological recovery in most cases. We present a case of eight months old baby who was diagnosed with a giant cavernoma resulting in secondary obstructive hydrocephalus with neuropsychiatric presentations. The patient underwent a paramedian craniotomy surgery with a suboccipital approach and complete surgical resection of the cavernoma was done. Over nine months of observation, the child showed improvement in their ability to walk and fully recovered from a neurological perspective. We also conducted a literature review to identify eleven cases of giant cerebellar cavernomas in children, including our case. The data were analyzed to determine the clinical features, treatment, and outcomes of giant cerebellar cavernomas in children.
Author	Kurbanov, Fuat Mukadasavoch Akramov, Olim Zaribovich Chaurasia, Bipin Tashmatov, Sukhrob Abdurashibovich Usmankhanov, Odilkhon Ayubxanovich Rakhimov, Ikrom Ismatovich Nazarova, Lilia Aleksandrovna
Author_xml	– sequence: 1 givenname: Olim Zaribovich surname: Akramov fullname: Akramov, Olim Zaribovich organization: Department of Neurosurgery, National Children's Medical Center, Ministry of Healthcare of Republic of Uzbekistan, Tashkent, Uzbekistan – sequence: 2 givenname: Lilia Aleksandrovna surname: Nazarova fullname: Nazarova, Lilia Aleksandrovna organization: Department of Neurosurgery, National Children's Medical Center, Ministry of Healthcare of Republic of Uzbekistan, Tashkent, Uzbekistan – sequence: 3 givenname: Fuat Mukadasavoch surname: Kurbanov fullname: Kurbanov, Fuat Mukadasavoch organization: Department of Neurosurgery, National Children's Medical Center, Ministry of Healthcare of Republic of Uzbekistan, Tashkent, Uzbekistan – sequence: 4 givenname: Sukhrob Abdurashibovich surname: Tashmatov fullname: Tashmatov, Sukhrob Abdurashibovich organization: Department of Neurosurgery, National Children's Medical Center, Ministry of Healthcare of Republic of Uzbekistan, Tashkent, Uzbekistan – sequence: 5 givenname: Ikrom Ismatovich surname: Rakhimov fullname: Rakhimov, Ikrom Ismatovich organization: Department of Neurosurgery, Tashkent Pediatric Medical Institute, Tashkent, Uzbekistan – sequence: 6 givenname: Odilkhon Ayubxanovich surname: Usmankhanov fullname: Usmankhanov, Odilkhon Ayubxanovich organization: Department of Neurosurgery, Tashkent Pediatric Medical Institute, Tashkent, Uzbekistan – sequence: 7 givenname: Bipin surname: Chaurasia fullname: Chaurasia, Bipin organization: Department of Neurosurgery, Neurosurgery Clinic, Birgunj, Nepal
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References	ref13 ref24 ref12 ref23 ref15 ref14 ref20 ref11 ref22 ref10 ref21 Avci (ref2) 2007 Atalar (ref1) 2007 Grujić (ref7) 2020 ref17 ref19 ref18 ref8 ref9 ref4 ref3 ref6 ref5 Otten (ref16) 1989
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