Cerebellar cavernoma excision with a preserved venous anomaly: A case report in girl 28-year-old
Cavernous malformations are congenital or acquired vascular abnormalities. They are uncommon entities with an incidence of 0.5 % of the general population and usually are unnoticed until a hemorrhagic event occurs. Cerebellar cavernomas (CCMs) account for 1.2 to 11.8 % of all intracranial cases and...
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Published in: | International journal of surgery case reports Vol. 107; p. 108332 |
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Abstract | Cavernous malformations are congenital or acquired vascular abnormalities. They are uncommon entities with an incidence of 0.5 % of the general population and usually are unnoticed until a hemorrhagic event occurs. Cerebellar cavernomas (CCMs) account for 1.2 to 11.8 % of all intracranial cases and 9.3 to 52.9 % of all infratentorial cases. Cavernomas can be concurrently seen with developmental venous anomalies (DVAs) in 20 % (range 20 %–40 %) of cases, in which case they are known as mixed vascular malformations.
We report a case of a healthy young adult who presented with acute onset of headache, with characteristics of chronic headache that gets progressively worse. The patient complains of frequent dizziness when sitting and standing for a long time. Complaints have been felt for two years and have worsened for the past two weeks. Additional complaints are dizziness and nausea with intermittent episodes of vomiting for four days. Magnetic resonance imaging (MRI) revealed an underlying cavernoma that had bled and a coexisting DVA. The patient was discharged home with no deficits. Outpatient follow-up two months later showed no symptoms or neurologic deficits.
Cavernous malformations are congenital or acquired vascular anomalies that occur in approximately 0.5 % of the general population. Our patient likely had dizziness due to localization of the bleeding of the cavernoma on the left side of the cerebellum. In our patient, brain imaging revealed numerous abnormal blood vessels radiating from the cerebellar lesion, a highly suggestive of DVAs associated with cavernoma.
A cavernous malformation is an uncommon entity that might coexist with deep venous anomalies, making management more challenging.
•Cavernous malformation is a benign vascular lesion in the CNS and other organs such as the liver or skin. The CNS cavernoma accounts for 5-13% of all intracranial vascular anomalies, and they vary in size from a few millimetres to a few centimetres in diameter.•A cavernous malformation is an uncommon entity that might coexist with deep venous anomalies, making management more challenging. |
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AbstractList | Cavernous malformations are congenital or acquired vascular abnormalities. They are uncommon entities with an incidence of 0.5 % of the general population and usually are unnoticed until a hemorrhagic event occurs. Cerebellar cavernomas (CCMs) account for 1.2 to 11.8 % of all intracranial cases and 9.3 to 52.9 % of all infratentorial cases. Cavernomas can be concurrently seen with developmental venous anomalies (DVAs) in 20 % (range 20 %-40 %) of cases, in which case they are known as mixed vascular malformations.
We report a case of a healthy young adult who presented with acute onset of headache, with characteristics of chronic headache that gets progressively worse. The patient complains of frequent dizziness when sitting and standing for a long time. Complaints have been felt for two years and have worsened for the past two weeks. Additional complaints are dizziness and nausea with intermittent episodes of vomiting for four days. Magnetic resonance imaging (MRI) revealed an underlying cavernoma that had bled and a coexisting DVA. The patient was discharged home with no deficits. Outpatient follow-up two months later showed no symptoms or neurologic deficits.
Cavernous malformations are congenital or acquired vascular anomalies that occur in approximately 0.5 % of the general population. Our patient likely had dizziness due to localization of the bleeding of the cavernoma on the left side of the cerebellum. In our patient, brain imaging revealed numerous abnormal blood vessels radiating from the cerebellar lesion, a highly suggestive of DVAs associated with cavernoma.
A cavernous malformation is an uncommon entity that might coexist with deep venous anomalies, making management more challenging. • Cavernous malformation is a benign vascular lesion in the CNS and other organs such as the liver or skin. The CNS cavernoma accounts for 5-13% of all intracranial vascular anomalies, and they vary in size from a few millimetres to a few centimetres in diameter. • A cavernous malformation is an uncommon entity that might coexist with deep venous anomalies, making management more challenging. Cavernous malformations are congenital or acquired vascular abnormalities. They are uncommon entities with an incidence of 0.5 % of the general population and usually are unnoticed until a hemorrhagic event occurs. Cerebellar cavernomas (CCMs) account for 1.2 to 11.8 % of all intracranial cases and 9.3 to 52.9 % of all infratentorial cases. Cavernomas can be concurrently seen with developmental venous anomalies (DVAs) in 20 % (range 20 %–40 %) of cases, in which case they are known as mixed vascular malformations. We report a case of a healthy young adult who presented with acute onset of headache, with characteristics of chronic headache that gets progressively worse. The patient complains of frequent dizziness when sitting and standing for a long time. Complaints have been felt for two years and have worsened for the past two weeks. Additional complaints are dizziness and nausea with intermittent episodes of vomiting for four days. Magnetic resonance imaging (MRI) revealed an underlying cavernoma that had bled and a coexisting DVA. The patient was discharged home with no deficits. Outpatient follow-up two months later showed no symptoms or neurologic deficits. Cavernous malformations are congenital or acquired vascular anomalies that occur in approximately 0.5 % of the general population. Our patient likely had dizziness due to localization of the bleeding of the cavernoma on the left side of the cerebellum. In our patient, brain imaging revealed numerous abnormal blood vessels radiating from the cerebellar lesion, a highly suggestive of DVAs associated with cavernoma. A cavernous malformation is an uncommon entity that might coexist with deep venous anomalies, making management more challenging. •Cavernous malformation is a benign vascular lesion in the CNS and other organs such as the liver or skin. The CNS cavernoma accounts for 5-13% of all intracranial vascular anomalies, and they vary in size from a few millimetres to a few centimetres in diameter.•A cavernous malformation is an uncommon entity that might coexist with deep venous anomalies, making management more challenging. |
ArticleNumber | 108332 |
Author | Fitra, Fitra Irsyad, Muhammad Ari Suroto, Nur Setiawan Al Fauzi, Asra Sanjaya, Firman Adi |
Author_xml | – sequence: 1 givenname: Muhammad Ari surname: Irsyad fullname: Irsyad, Muhammad Ari email: dokter.irsyad@gmail.com organization: Universitas Sumatera Utara Hospital, Medan, Indonesia – sequence: 2 givenname: Fitra surname: Fitra fullname: Fitra, Fitra organization: Department of Neurosurgery, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia – sequence: 3 givenname: Firman Adi surname: Sanjaya fullname: Sanjaya, Firman Adi organization: Department of Neurosurgery, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia – sequence: 4 givenname: Nur Setiawan surname: Suroto fullname: Suroto, Nur Setiawan organization: Department of Neurosurgery, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia – sequence: 5 givenname: Asra surname: Al Fauzi fullname: Al Fauzi, Asra organization: Department of Neurosurgery, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37269764$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1111/j.1742-4658.2009.07535.x 10.1161/STROKEAHA.118.022314 10.7759/cureus.5412 10.1007/s00701-007-1455-z 10.1186/1471-2377-13-134 10.1093/neuros/nyx091 10.1001/jamaneurol.2017.0439 10.1056/NEJMra052760 10.1007/s00701-008-1570-5 10.1111/jon.12373 10.1016/j.ijsu.2020.10.034 10.1177/1747493017694393 10.4274/tnd.65928 10.1159/000486292 |
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Keywords | Severe headache Cerebral cavernoma Venous anomaly |
Language | English |
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References | Huang, Guo, Shi, Yang, Rao (bb0015) 2017; 12 Akers, Al-Shahi Salman, Awad, Awad, Flemming, Hart (bb0050) 2017; 80 Abla, Wait, Uschold, Lekovic, Spetzler (bb0020) 2008 May; 150 Flemming, Graff-Radford, Aakre, Kantarci, Lanzino, Brown (bb0060) 2017; 74 Agha, Franchi, Sohrabi, Mathew, for the SCARE Group (bb0070) 2020; 84 Mullaguri, Battineni, Krishnaiah, Ibrahim, Newey (bb0025) 2019 Maeder, Gudinchet, Meuli, de Tribolet (bb0040) 1998; 19 Riant, Bergametti, Ayrignac, Boulay, Tournier-Lasserve (bb0045) 2010; 277 Zafar, Quadri, Farooqui, Ikram, Robinson, Hart (bb0055) 2019 May; 50 Zhang, Liu, Cao, Wang, Zhao (bb0010) 2013; 13 Ligha, Robert (bb0080) 2017; 23 Nabavizadeh, Mamourian, Vossough, Loevner, Hurst (bb0030) 2016 Sep; 26 Spiegler, Rath, Paperlein, Felber (bb0065) 2018; 9 Kan, Tubay, Osborn, Blaser, Cloudwell (bb0075) 2008; 150 Brisman, Song, Newell (bb0005) 2006; 355 Brisman (10.1016/j.ijscr.2023.108332_bb0005) 2006; 355 Kan (10.1016/j.ijscr.2023.108332_bb0075) 2008; 150 Ligha (10.1016/j.ijscr.2023.108332_bb0080) 2017; 23 Agha (10.1016/j.ijscr.2023.108332_bb0070) 2020; 84 Akers (10.1016/j.ijscr.2023.108332_bb0050) 2017; 80 Maeder (10.1016/j.ijscr.2023.108332_bb0040) 1998; 19 Huang (10.1016/j.ijscr.2023.108332_bb0015) 2017; 12 Flemming (10.1016/j.ijscr.2023.108332_bb0060) 2017; 74 Mullaguri (10.1016/j.ijscr.2023.108332_bb0025) 2019 Abla (10.1016/j.ijscr.2023.108332_bb0020) 2008; 150 Zafar (10.1016/j.ijscr.2023.108332_bb0055) 2019; 50 Spiegler (10.1016/j.ijscr.2023.108332_bb0065) 2018; 9 Riant (10.1016/j.ijscr.2023.108332_bb0045) 2010; 277 Zhang (10.1016/j.ijscr.2023.108332_bb0010) 2013; 13 Nabavizadeh (10.1016/j.ijscr.2023.108332_bb0030) 2016; 26 |
References_xml | – volume: 355 start-page: 928 year: 2006 end-page: 939 ident: bb0005 article-title: Cerebral aneurysms publication-title: N. Engl. J. Med. contributor: fullname: Newell – volume: 12 start-page: 246 year: 2017 end-page: 253 ident: bb0015 article-title: Etiology and pathogenesis of Moyamoya disease: an update on disease prevalence publication-title: Int. J. Stroke contributor: fullname: Rao – volume: 9 start-page: 60 year: 2018 end-page: 69 ident: bb0065 article-title: Cerebral cavernous malformations: an update on prevalence, molecular genetic analyses, and counselling publication-title: Mol. Syndrome contributor: fullname: Felber – volume: 74 start-page: 801 year: 2017 end-page: 805 ident: bb0060 article-title: Population-based prevalence of cavernous cerebral malformations in older adults: mayo clinic study of ageing publication-title: JAMA Neurol. contributor: fullname: Brown – volume: 26 start-page: 463 year: 2016 Sep end-page: 472 ident: bb0030 article-title: The many faces of cerebral developmental venous anomaly and its mimics: spectrum of imaging findings publication-title: J. Neuroimaging contributor: fullname: Hurst – volume: 13 start-page: 1 year: 2013 end-page: 8 ident: bb0010 article-title: Cerebellar cavernous malformations with and without associated developmental venous anomalies publication-title: BMC Neurol. contributor: fullname: Zhao – volume: 150 start-page: 487 year: 2008 May end-page: 489 ident: bb0020 article-title: Developmental venous anomaly, cavernous malformation, and capillary telangiectasia: spectrum of a single disease publication-title: Acta Neurochir. contributor: fullname: Spetzler – volume: 50 start-page: 1294 year: 2019 May end-page: 1301 ident: bb0055 article-title: Familial cerebral cavernous malformations publication-title: Stroke contributor: fullname: Hart – volume: 277 start-page: 1070 year: 2010 end-page: 1075 ident: bb0045 article-title: Recent insights into cavernous cerebral malformations: the molecular genetics of CCM publication-title: FEBS J. contributor: fullname: Tournier-Lasserve – volume: 150 start-page: 49 year: 2008 end-page: 55 ident: bb0075 article-title: Radiographic features of tumefactive giant cavernous angiomas publication-title: Acta Neurochir. contributor: fullname: Cloudwell – volume: 23 start-page: 234 year: 2017 end-page: 238 ident: bb0080 article-title: Medusa-like atypical intracerebral vein: a rare case of symptomatic developmental venous anomaly publication-title: Turk. J. Neurol. contributor: fullname: Robert – year: 2019 ident: bb0025 article-title: Developmental venous anomaly presenting with spontaneous intracerbral hemorrhage, acute ischemic stroke, and seizure publication-title: Cureus contributor: fullname: Newey – volume: 84 start-page: 226 year: 2020 end-page: 230 ident: bb0070 article-title: The SCARE 2020 guideline: updating consensus surgical case report (SCARE) guidelines publication-title: Int. J. Surg. contributor: fullname: for the SCARE Group – volume: 19 start-page: 1141 year: 1998 end-page: 1143 ident: bb0040 article-title: Development of a cavernous malformation of the brain publication-title: AJNR Am. J. Neuroradiol. contributor: fullname: de Tribolet – volume: 80 start-page: 665 year: 2017 end-page: 680 ident: bb0050 article-title: Synopsis of guidelines for the clinical management of cavernous cerebral malformations: consensus recommendations based on systematic literature review by the angioma alliance scientific advisory board clinical experts panel publication-title: Neurosurgery contributor: fullname: Hart – volume: 19 start-page: 1141 issue: 6 year: 1998 ident: 10.1016/j.ijscr.2023.108332_bb0040 article-title: Development of a cavernous malformation of the brain publication-title: AJNR Am. J. Neuroradiol. contributor: fullname: Maeder – volume: 277 start-page: 1070 issue: 5 year: 2010 ident: 10.1016/j.ijscr.2023.108332_bb0045 article-title: Recent insights into cavernous cerebral malformations: the molecular genetics of CCM publication-title: FEBS J. doi: 10.1111/j.1742-4658.2009.07535.x contributor: fullname: Riant – volume: 50 start-page: 1294 issue: 5 year: 2019 ident: 10.1016/j.ijscr.2023.108332_bb0055 article-title: Familial cerebral cavernous malformations publication-title: Stroke doi: 10.1161/STROKEAHA.118.022314 contributor: fullname: Zafar – year: 2019 ident: 10.1016/j.ijscr.2023.108332_bb0025 article-title: Developmental venous anomaly presenting with spontaneous intracerbral hemorrhage, acute ischemic stroke, and seizure publication-title: Cureus doi: 10.7759/cureus.5412 contributor: fullname: Mullaguri – volume: 150 start-page: 49 year: 2008 ident: 10.1016/j.ijscr.2023.108332_bb0075 article-title: Radiographic features of tumefactive giant cavernous angiomas publication-title: Acta Neurochir. doi: 10.1007/s00701-007-1455-z contributor: fullname: Kan – volume: 13 start-page: 1 issue: 1 year: 2013 ident: 10.1016/j.ijscr.2023.108332_bb0010 article-title: Cerebellar cavernous malformations with and without associated developmental venous anomalies publication-title: BMC Neurol. doi: 10.1186/1471-2377-13-134 contributor: fullname: Zhang – volume: 80 start-page: 665 issue: 5 year: 2017 ident: 10.1016/j.ijscr.2023.108332_bb0050 article-title: Synopsis of guidelines for the clinical management of cavernous cerebral malformations: consensus recommendations based on systematic literature review by the angioma alliance scientific advisory board clinical experts panel publication-title: Neurosurgery doi: 10.1093/neuros/nyx091 contributor: fullname: Akers – volume: 74 start-page: 801 issue: 7 year: 2017 ident: 10.1016/j.ijscr.2023.108332_bb0060 article-title: Population-based prevalence of cavernous cerebral malformations in older adults: mayo clinic study of ageing publication-title: JAMA Neurol. doi: 10.1001/jamaneurol.2017.0439 contributor: fullname: Flemming – volume: 355 start-page: 928 issue: 9 year: 2006 ident: 10.1016/j.ijscr.2023.108332_bb0005 article-title: Cerebral aneurysms publication-title: N. Engl. J. Med. doi: 10.1056/NEJMra052760 contributor: fullname: Brisman – volume: 150 start-page: 487 issue: 5 year: 2008 ident: 10.1016/j.ijscr.2023.108332_bb0020 article-title: Developmental venous anomaly, cavernous malformation, and capillary telangiectasia: spectrum of a single disease publication-title: Acta Neurochir. doi: 10.1007/s00701-008-1570-5 contributor: fullname: Abla – volume: 26 start-page: 463 issue: 5 year: 2016 ident: 10.1016/j.ijscr.2023.108332_bb0030 article-title: The many faces of cerebral developmental venous anomaly and its mimics: spectrum of imaging findings publication-title: J. Neuroimaging doi: 10.1111/jon.12373 contributor: fullname: Nabavizadeh – volume: 84 start-page: 226 year: 2020 ident: 10.1016/j.ijscr.2023.108332_bb0070 article-title: The SCARE 2020 guideline: updating consensus surgical case report (SCARE) guidelines publication-title: Int. J. Surg. doi: 10.1016/j.ijsu.2020.10.034 contributor: fullname: Agha – volume: 12 start-page: 246 issue: 3 year: 2017 ident: 10.1016/j.ijscr.2023.108332_bb0015 article-title: Etiology and pathogenesis of Moyamoya disease: an update on disease prevalence publication-title: Int. J. Stroke doi: 10.1177/1747493017694393 contributor: fullname: Huang – volume: 23 start-page: 234 year: 2017 ident: 10.1016/j.ijscr.2023.108332_bb0080 article-title: Medusa-like atypical intracerebral vein: a rare case of symptomatic developmental venous anomaly publication-title: Turk. J. Neurol. doi: 10.4274/tnd.65928 contributor: fullname: Ligha – volume: 9 start-page: 60 issue: 2 year: 2018 ident: 10.1016/j.ijscr.2023.108332_bb0065 article-title: Cerebral cavernous malformations: an update on prevalence, molecular genetic analyses, and counselling publication-title: Mol. Syndrome doi: 10.1159/000486292 contributor: fullname: Spiegler |
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Snippet | Cavernous malformations are congenital or acquired vascular abnormalities. They are uncommon entities with an incidence of 0.5 % of the general population and... • Cavernous malformation is a benign vascular lesion in the CNS and other organs such as the liver or skin. The CNS cavernoma accounts for 5-13% of all... |
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SubjectTerms | Case Report Cerebral cavernoma Severe headache Venous anomaly |
Title | Cerebellar cavernoma excision with a preserved venous anomaly: A case report in girl 28-year-old |
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