Abstract
Background
Cavernous angiomas are vascular malformations which rarely involve the cavities of the lateral ventricles. Knowledge of the specific clinical and neuroradiological features displayed by these lesions is limited by the scarcity of patients included in the reported series.
Objective and methods
The aim of this study was to compile and analyse the epidemiological, clinical, neuroradiological and surgical characteristics of these lesions as provided by the well-described examples reported in the scientific literature. A total of 49 were gathered, including three patients operated on recently in our Department.
Findings and conclusions
Cavernomas developing within the ventricular cavities attain a larger size than parenchymal counterpart lesions, causing symptoms and signs derived mainly from the mass effect. The characteristic parenchymal hypointense rim is less frequently identified on T2-weighted echo-gradient MRI sequences. Total surgical excision is the treatment of choice for these lesions, yet the surgical routes employed may still be associated with a high rate of neurological complications.
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References
Alves de Sousa A (2007) Cavernomes profonds (corps calleux, intraventriculaires, ganglions de la base, insulaires) et du tronc cérébral. Expérience d´une série brésilienne. Neurochirurgie 53:182–191
Arnstein LH, Boldrey E, Naffziger HC (1951) A case report and survey of brain tumours during the neonatal period. J Neurosurg 8:315–319
Attar A, Ugur HC, Savas A, Yüceer N, Egemen N (2001) Surgical treatment of intracranial cavernous angiomas. J Clin Neurosci 8(3):235–239
Chadduck WM, Binet EF, Farrell FW Jr, Araoz CA, Reding DL (1985) Intraventricular cavernous haemangioma: report of three cases and review of the literature. Neurosurgery 16:189–197
Coin CG, Coin JW, Glover MB (1977) Vascular tumours of the choroid plexus: diagnosis by computed tomography. J Comput Assist Tomogr 1:146–148
D’Angelo VA, Galarza M, Catapano D, Monte V, Bisceglia M, Carosi I (2005) Lateral ventricle tumours: surgical strategies according to tumour origin and development—a series of 72 patients. Neurosurgery 56(ONS Suppl 1):36–45
Fagundes-Pereyra WJ, Pinheiro Marques JA, de Sousa L, Cardoso de Carvalho GT, Alves de Sousa A (2000) Cavernoma do ventriculo lateral. Relato de caso. ArqNeuropsiquiatr 58(3–B):958–964
Finkelnburg R (1905) Differentialdiagnose zwischen Kleinhirntumoren und chronischem Hydrocephalus: Zugleich ein Beitrag zur Kenntnis der Angiome des Zentralnervensystems. Dtsch Z Nervenheilkd 29:135–151
González Darder JM, Pesudo Martínez JV, Merino Peña J (2007) Angioma cavernoso del trígono ventricular. Caso clínico. Neurocirugía (Astur) 18:330–332
Houtteville JP (1997) Brain cavernoma: a dynamic lesion. Surg Neurol 46:610–614
Houtteville JP (2007) Cavernomas of the central nervous system. Historical data and changing ideas. Neurochirurgie 53(2−3 Pt 2):117–121
Iwasa H, Indei I, Sato F (1983) Intra-ventricular cavernous haemangioma: case report. J Neurosurg 59:153–157
Jain KK (1966) Intra-ventricular cavernous haemangioma of the lateral ventricle. J Neurosurg 24:762–764
Jelinek J, Smirniotopoulos JG, Parisi JE, Kanzer M (1990) Lateral ventricular neoplasms of the brain: differential diagnosis based on clinical, CT, and MR findings. AJNR 11:567–574
Kaim A, Kirsch E, Tolnay M, Steinbrich W, Radü EW (1997) Foramen of Monro mass: MRI appearances permit diagnosis of cavernous haemangioma. Neuroradiology 39:265–269
Koeller KK, Sandberg GD (2002) Cerebral intraventricular neoplasms: radiologic–pathologic correlation. RadioGraphics 22:1473–1505
Kondziolka D, Lunsford LD, Kestle JRW (1995) The natural history of cerebral cavernous malformations. J Neurosurg 83:820–824
Kumar GSS, Poonnoose SI, Chacko AG, Rajshekhar V (2006) Trigonal cavernous angiomas: report of three cases and review of literature. Surg Neurol 65:367–371
Lynch JC, Andrade R, Pereira C, Salomao JF, Duarte F, Carvalho FG, Chadrycki E (1994) Angioma cavernoso intracraniano. Arq Neuropsiquiatr 52:224–237
McConnell TH, Leonard JS (1967) Microangiomatous malformations with intra-ventricular haemorrhage. Neurology 17:618–620
McGuire TH, Greenwood J, Newton B (1954) Bilateral angioma of choroid plexus. J Neurosurg 11:428–430
Merrit HH (1940) Case records of the Massachusetts General Hospital. N Engl J Med 222:191–195
Michaelson PG, Warren WL, DeLone DR, Quigley MR (2004) Intra-ventricular cavernous angioma. Appl Radiol 33(12):38–40
Miyagi Y, Mannoji H, Akaboshi K, Morioka T, Fukui M (1993) Intra-ventricular cavernous malformation associated with medullary venous malformation. Neurosurgery 32:461–464
Namba S, Ishimitsu H, Nakasone S (1979) Cavernous haemangioma of the brain. No Shinkei Geka 7:277–283
Nieto J, Hinojosa J, Muñoz MJ, Esparza J, Ricoy J (2003) Intra-ventricular cavernomas in paediatric age. Childs Nerv Syst 19:60–62
Notelet L, Houtteville JP, Khouri S, Lechevalier B, Chapon F (1997) Proliferative Cell Nuclear Antigen (PCNA) in cerebral cavernomas: an immuno-cytochemical study of 42 cases. Surg Neurol 7:364–370
Numaguchi Y, Fukui M, Miyake E, Kishikawa T, Ikeda J, Matsura K, Tomonaga M, Kitamura K (1977) Angiographic manifestations of intracerebral cavernous haemangioma. Neuroradiology 14:113–116
Pau A, Orunesu G (1979) Vascular malformation of the brain in achondroplasia. Acta Neurochir (Wien) 50:289–292
Reyns N, Assaker R, Louis E, Lejeune JP (2000) Intra-ventricular cavernomas: three cases and review of the literature. Neurosurgery 44(3):648–654
Rothon ALJ (2002) The lateral and third ventricles. Neurosurgery 51(Suppl 1):207–271
Sabatier J, Gigaud M, Dubois G, Tremoulet M (1989) Cavernoma in the child. Apropos of a neonatal form with recurrence in the childhood. Neurochirurgie 35:109–110
Schneider RC, Liss L (1958) Cavernous haemangioma of the cerebral hemispheres. J Neurosurg 15:392–399
Sedan R, Peragut JC, Fabrici A (1989) Cavernomas and stereotactic surgery. Neurochirurgie 35:126–127
Simard JM, García-Bengochea F, Ballinger WE, Mickle JP, Quisling RG (1986) Cavernous angioma: a review of 126 collected and 12 new clinical cases. Neurosurgery 18:162–172
Suzuki J (1988) Bifrontal anterior interhemispheric approach. In: Apuzzo MLJ (ed) Surgery of the third ventricle. Williams & Wilkins, Baltimore, pp. 489–515
Tatagiba M, Schönmayr R, Samii M (1991) Intra-ventricular cavernous angioma: a survey. Acta Neurochir (Wien) 110:140–145
Tatsui CE, Koerbel A, Prevedello DM, Hanel RA, Grande CV, Moro MS, Araújo JC (2003) Ressonancia magnética dos cavernomas intra-ventriculares. Arq Neuropsiquiatr 61(1):79–82
Towfighi J, Bilaniuk T, Zimmerman RA, Langfitt TW, Gonatas NK (1976) Haemorrhages in bilateral choroid plexus haemangiomas demonstrated by computed tomography. J Neurosurg 45:218–222
Voigt K, Yasargil MG (1976) Cerebral cavernous haemangiomas or cavernomas. Neurochirurgia (Stuttg) 19:59–68
Yamasaki T, Handa H, Yamashita J, Paine JT, Tashiro Y, Uno A, Ishikawa M, Asato R (1986) Intracranial and orbital cavernous angiomas: a review of 30 cases. J Neurosurg 64:197–208
Yasargil MG, Teddy PJ, Roth P (1985) Selective amygdalohippocampectomy. Operative anatomy and surgical technique. In: Symon L, Brihaye J, Guidetti B (eds) Advances and technical standards in neurosurgery, vol. 12. SpringerVerlag, Wien, pp 93–123
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We wish to acknowledge Prof. Sara Cowburn for her careful revision of the English language and style of the manuscript.
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Comment
Carrasco et al reported three rare cases of the lateral ventricle CM and had the systematic review of the whole reported similar cases in the literature. They analyzed the radiological findings, surgical strategies and the outcomes of these lesions. They concluded that radical surgery was still the treatment of choice, with low mortality but high neurological morbidity. This report offered the general outline of this rare subgroup of cavernoma.
But the definition of ventricle cavernoma is still not clear. Actually many lesions are the cavernoma arising from the thalamus or basal ganglia.
Intralesional hemorrhages and lesion expansion may involve the lateral wall of the ventricle and protrude into the ventricle cativity. In the case of thalamus cavernoma, it is not uncommon in the clinical experience.
Surgical treatment of the CM in that area should be carefully balanced between the outcome and the natural course. Accurate localization of the lesions with neuronavigation can offer individualized surgical approaches and avoid additional surgical trauma to the eloquent area. We agree that radical resection of the lesions is the treatment of choice. Partial resection of the lesion or biopsy is not recommended.
Ying Mao
Hua Shan Hospital, Shanghai
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Carrasco, R., Pedrosa, M., Pascual, J.M. et al. Cavernous angiomas of the lateral ventricles. Acta Neurochir (Wien) 151, 149–154 (2009). https://doi.org/10.1007/s00701-009-0186-8
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DOI: https://doi.org/10.1007/s00701-009-0186-8