Öz
Cerebral cavernous hemangiomas are rarely seen malformations of vascular stuctures. While sporadic forms usually single lesions, multiple lesions are more common familial type of situation. Symptomatic patients with headache, epileptic seizure, focal neurological deficits, hemorrhage, or combinations of these apply to the hospital. Our case differs from the cases presented in the literature, because it has infratentorial involvement beside multiple supratentorial lesions and our case with multiple cavernoma is not hereditary.
Anahtar Kelimeler
Epileptic seizure hereditary infratentorial cavernous hemangioma
Kaynakça
- Smit LM, Halbertsma FJ. Cerebral cavernous hemangiomas in childhood. Clinical presentation and therapeutic considerations. Childs Nerv Syst 1997; 13: 522Mao Y, Zhao Y, Zhou LF, Huang CX, Shou XF, Gong JL, Lawton MT, Yang GY. A novel gene mutation (1292 deletion) in a Chinese family with cerebral cavernous malformations. Neurosurgery 2005; 56: 1149-53.
- Moriarity JL, Clatterbuck RE, Rigamonti D. The natural history of cavernous malformations. Neurosurg Clin N Am 1999; 10: 411-7.
- Zabramski JM, Henn JS, Coons S. Pathology of cerebral vascular malformations. Neurosurg Clin N Am 1999; 10: 395-410.
- İplikçioğlu AC, Benli K, Bertan V, Ruacan S. Cystic cavernous hemangioma of the cerebellopontine angle: case report. Neurosurgery 1986; 19: 641-2. de Oliveira JG, Rassi-Neto A, Ferraz FA, Braga FM. Neurosurgical management of cerebellar cavernous malformations. Neurosurg Focus 2006; 15; 21: e-11.
- Robinson JR, Awad IA, Little JR. Natural history of the cavernous angioma. J Neurosurg 1991; 75: 709-14.
- Russel DS, Rubinstein LJ. Pathology of tumors of the nervous system: Tumor and hamartoma of the blood vessels, üçüncü baskı, London: Edward Arnold, 1971; 85-108.
- Sakai N, Yamada H, Tanigawara T, Asano Y, Andoh T, Tanabe Y, Takada M. Surgical treatment of cavernous angioma involving the brainstem and review of the literature. Acta Neurochir 1991; 113: 138-43.
- Porter PJ, Willinsky RA, Harper W, Wallace MC. Cerebral cavernous malformations: Natural history and prognosis after clinical deterioration with or without hemorrhage. J Neurosurg 1997; 87: 190-7.
- Otten P, Pizzolato GP, Rilliet B, Berney J. 131 cases of cavernous angioma (cavernomas) of the CNS, discovered by retrospective analysis of 24,535 autopsies. Neurochirurgie 1989; 35: 82-3,128-31.
- Del Curling O Jr, Kelly DL Jr, Elster AD, Craven TE. An analysis of the natural history of cavernous angiomas. J Neurosurg 1991; 75: 702-8.
- Craig HD, Günel M, Cepeda O, Johnson EW, Ptacek L, Steinberg GK, Ogilvy CS, Berg MJ, Crawford SC, Scott RM, Steichen-Gersdorf E, Sabroe R, Kennedy CT, Mettler G, Beis MJ, Fryer A, Awad IA, Lifton RP. Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27. Hum Mol Genet 1998; 7: 1851-8.
- Dubovsky J, Zabramski JM, Kurth J, Spetzler RF, Rich SS, Orr HT, Weber JL. A gene responsible for cavernous malformations of the brain maps to chromosome 7q. Hum Mol Genet 1995; 4: 453-8.
- Rigamonti D, Johnson PC, Spetzler RF, Hadley MN, Drayer BP. Cavernous malformations and capillary telangiectasia: A spectrum within a single pathological entity. Neurosurgery 1991; 28: 60-4.
- Hausler R, Levine RA. Auditory dysfunction in stroke. Acta Otolaryngol 2000; 120: 689-703.
- Simard JM, Garcia-Bengochea F, Ballinger WE Jr, Mickle JP, Quisling RG. Cavernous angioma: a review of 126 collected and 12 new clinical cases. Neurosurgery 1986; 18: 162-72.
- Johnson PC, Wascher TM, Golfinos J, Spetzler RF. Definition and pathological features. In: Awad IA, Barrow DL, eds. Cavernous Malformations: American Association of Neurological Surgeons, Publications Committee; 1993: 1-11.
- Brown RD Jr, Wiebers DO, Torner JC, O'Fallon WM. Incidence and prevalence of intracranial vascular malformations in Olmsted County, Minnesota, 1965 to 199 Neurology 1996; 46: 949-52.
- Fritschi JA, Reulen HJ, Spetzler RF, Zabramski JM. Cavernous malformations of the brain stem. A review of 139 cases. Acta Neurochir (Wien) 1994; 130: 35-46. Labauge P, Brunereau L, Laberge S, Houtteville JP. Prospective follow-up of 33 asymptomatic patients with familial cerebral cavernous malformations. Neurology 2001; 57: 1825-8.
- Zabramski JM, Wascher TM, Spetzler RF, Johnson B, Golfinos J, Drayer BP, Brown B, Rigamonti D, Brown G. The natural history of familial cavernous malformations: results of an ongoing study. J Neurosurg 1994; 80: 422-32.
- Brunereau L, Labauge P, Tournier-Lasserve E, Laberge S, Levy C, Houtteville JP. Radiology 2000; 214: 209-16.
Öz
Özet
Serebral kavernöz hemanjiomlar vasküler yapıların nadir görülen malformasyonlarındandır. Sporadik formda lezyonlar genellikle tek iken, lezyonların multipl olması daha çok familyal tipte rastlanılan bir durumdur. Semptomatik hastalar başağrısı, epileptik nöbet, fokal nörolojik defisit, hemoraji veya bunların kombinasyonu ile hastaneye başvururlar. Bizim olgumuz multiple supratentoryal lezyonların yanı sıra infratentoryal tutulumun da birlikte görülmesi ve multiple kavernom olmasına rağmen herediter geçişli olmaması nedeniyle literatürdeki sunumlardan farklılık göstermektedir.
Anahtar sözcükler: Epileptik nöbet, herediter, infratentorial, kavernöz hemanjiom
Abstract
Cerebral cavernous hemangiomas are rarely seen malformations of vascular stuctures. While sporadic forms usually single lesions, multiple lesions are more common familial type of situation. Symptomatic patients with headache, epileptic seizure, focal neurological deficits, hemorrhage, or combinations of these apply to the hospital. Our case differs from the cases presented in the literature, because it has infratentorial involvement beside multiple supratentorial lesions and our case with multiple cavernoma is not hereditary.
Keywords: Epileptic seizure, hereditary, infratentorial, cavernous hemangioma
Anahtar Kelimeler
Kaynakça
- Smit LM, Halbertsma FJ. Cerebral cavernous hemangiomas in childhood. Clinical presentation and therapeutic considerations. Childs Nerv Syst 1997; 13: 522Mao Y, Zhao Y, Zhou LF, Huang CX, Shou XF, Gong JL, Lawton MT, Yang GY. A novel gene mutation (1292 deletion) in a Chinese family with cerebral cavernous malformations. Neurosurgery 2005; 56: 1149-53.
- Moriarity JL, Clatterbuck RE, Rigamonti D. The natural history of cavernous malformations. Neurosurg Clin N Am 1999; 10: 411-7.
- Zabramski JM, Henn JS, Coons S. Pathology of cerebral vascular malformations. Neurosurg Clin N Am 1999; 10: 395-410.
- İplikçioğlu AC, Benli K, Bertan V, Ruacan S. Cystic cavernous hemangioma of the cerebellopontine angle: case report. Neurosurgery 1986; 19: 641-2. de Oliveira JG, Rassi-Neto A, Ferraz FA, Braga FM. Neurosurgical management of cerebellar cavernous malformations. Neurosurg Focus 2006; 15; 21: e-11.
- Robinson JR, Awad IA, Little JR. Natural history of the cavernous angioma. J Neurosurg 1991; 75: 709-14.
- Russel DS, Rubinstein LJ. Pathology of tumors of the nervous system: Tumor and hamartoma of the blood vessels, üçüncü baskı, London: Edward Arnold, 1971; 85-108.
- Sakai N, Yamada H, Tanigawara T, Asano Y, Andoh T, Tanabe Y, Takada M. Surgical treatment of cavernous angioma involving the brainstem and review of the literature. Acta Neurochir 1991; 113: 138-43.
- Porter PJ, Willinsky RA, Harper W, Wallace MC. Cerebral cavernous malformations: Natural history and prognosis after clinical deterioration with or without hemorrhage. J Neurosurg 1997; 87: 190-7.
- Otten P, Pizzolato GP, Rilliet B, Berney J. 131 cases of cavernous angioma (cavernomas) of the CNS, discovered by retrospective analysis of 24,535 autopsies. Neurochirurgie 1989; 35: 82-3,128-31.
- Del Curling O Jr, Kelly DL Jr, Elster AD, Craven TE. An analysis of the natural history of cavernous angiomas. J Neurosurg 1991; 75: 702-8.
- Craig HD, Günel M, Cepeda O, Johnson EW, Ptacek L, Steinberg GK, Ogilvy CS, Berg MJ, Crawford SC, Scott RM, Steichen-Gersdorf E, Sabroe R, Kennedy CT, Mettler G, Beis MJ, Fryer A, Awad IA, Lifton RP. Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27. Hum Mol Genet 1998; 7: 1851-8.
- Dubovsky J, Zabramski JM, Kurth J, Spetzler RF, Rich SS, Orr HT, Weber JL. A gene responsible for cavernous malformations of the brain maps to chromosome 7q. Hum Mol Genet 1995; 4: 453-8.
- Rigamonti D, Johnson PC, Spetzler RF, Hadley MN, Drayer BP. Cavernous malformations and capillary telangiectasia: A spectrum within a single pathological entity. Neurosurgery 1991; 28: 60-4.
- Hausler R, Levine RA. Auditory dysfunction in stroke. Acta Otolaryngol 2000; 120: 689-703.
- Simard JM, Garcia-Bengochea F, Ballinger WE Jr, Mickle JP, Quisling RG. Cavernous angioma: a review of 126 collected and 12 new clinical cases. Neurosurgery 1986; 18: 162-72.
- Johnson PC, Wascher TM, Golfinos J, Spetzler RF. Definition and pathological features. In: Awad IA, Barrow DL, eds. Cavernous Malformations: American Association of Neurological Surgeons, Publications Committee; 1993: 1-11.
- Brown RD Jr, Wiebers DO, Torner JC, O'Fallon WM. Incidence and prevalence of intracranial vascular malformations in Olmsted County, Minnesota, 1965 to 199 Neurology 1996; 46: 949-52.
- Fritschi JA, Reulen HJ, Spetzler RF, Zabramski JM. Cavernous malformations of the brain stem. A review of 139 cases. Acta Neurochir (Wien) 1994; 130: 35-46. Labauge P, Brunereau L, Laberge S, Houtteville JP. Prospective follow-up of 33 asymptomatic patients with familial cerebral cavernous malformations. Neurology 2001; 57: 1825-8.
- Zabramski JM, Wascher TM, Spetzler RF, Johnson B, Golfinos J, Drayer BP, Brown B, Rigamonti D, Brown G. The natural history of familial cavernous malformations: results of an ongoing study. J Neurosurg 1994; 80: 422-32.
- Brunereau L, Labauge P, Tournier-Lasserve E, Laberge S, Levy C, Houtteville JP. Radiology 2000; 214: 209-16.
Ayrıntılar
| Birincil Dil | Türkçe |
|---|---|
| Bölüm | Olgu Sunumları |
| Yazarlar | |
| Yayımlanma Tarihi | 22 Mart 2013 |
| Yayımlandığı Sayı | Yıl 2013Cilt: 35 Sayı: 1 |