- Research article
- Open Access
- Open Peer Review
Cerebellar cavernous malformations with and without associated developmental venous anomalies
© Zhang et al.; licensee BioMed Central Ltd. 2013
- Received: 13 March 2013
- Accepted: 18 September 2013
- Published: 3 October 2013
The clinical profiles of cerebellar cavernous malformations (CCMs) with and without associated developmental venous anomalies (DVAs) are not well known. The aims of this study were to analyze the clinical and radiological characteristics of CCMs and to assess the various therapeutic strategies.
A consecutive series of 41 patients with identified CCMs were retrospectively reviewed. Of these, 11 patients (26.8%) were found to have associated DVAs. We compared the clinical profile of the two groups of patients (CCMs with and without DVAs). The CCMs with DVAs cases underwent radical resection of the CCMs, and the distal radicles of the DVAs that directly drain from the CCMs were coagulated and dissected at the length of the CCMs.
There were no statistically significant differences between the two groups with regard to age, sex, location and size of lesions, multiplicity, and surgical prognosis. The patients with CCMs with DVAs did not experience any brain swelling or hemorrhagic tendency intraoperatively. The postoperative course was uneventful for all of the 36 surgical patients with the exception of two of the patients with CCMs with associated DVAs, who suffered from serious cerebellar edema, and one of these two patients underwent an emergency suboccipital decompression craniotomy. With the exception of three patients who were lost to follow-up (mean, 22.3 months), all of the CCMs patients exhibited good long-term prognosis (modified Rankin scale values of 0–2) and no reoccurrence.
It is not rare that associated DVAs occur in CCMs. The total removal of the CCM combined with the coagulation and dissection of the distal radicles of DVA at the length of the associated CCM may result in good long-term prognosis in patients.
- Cavernous malformations
- Developmental venous anomalies
The incidence rate of cavernous malformations (CMs) ranges from 0.4 to 0.9% of the general population. These incidences constitute 8 to 15% of all cerebrovascular malformations [1–5] and occur in the supratentorial compartment in 63 to 90% of cases [6, 7]. Posterior fossa CMs represent 7.8 to 35.8% of all cases, and the brainstem is the most commonly involved site in this compartment (9-35% of all cases) [4, 7]. Based on a large sample size, cerebellar CMs (CCMs) constitute 1.2 to 11.8% of all intracranial cases and 9.3 to 52.9% of all infratentorial cases [7, 8]. The current data in the literature regarding CMs localized in the cerebellum are limited to case reports [7, 9–12].
The coexistence of a CM and an associated developmental venous anomaly (DVA) is the most common mixed vascular malformation . Patients with CMs associated with DVAs are more likely to have lesions in the posterior fossa . The difference in the clinical profiles and surgical outcome between patients with CMs with and without associated DVAs in the cerebellum is unclear, which makes it difficult to determine the long-term prognosis of these patients.
There is controversy regarding the management of CMs associated with DVAs. Recent findings support the hypothesis that DVAs can be considered the initial pathophysiological factor that leads to the formation of CMs [14–18]. Additionally, some authors have proposed the coagulation and division of the transcerebral vein of the DVA during the removal of the CM as a means to prevent the recurrence of CMs . However, due to the compromise of venous drainage of normal cerebellum, this strategy might increase the risk of serious postoperative cerebellar edema and might even cause cerebellar tonsillar herniation. The identification of a balance between the recurrence of the associated CM and herniation, which is a devastating consequence, currently remains unknown.
We retrospectively reviewed 41 patients suffering from cerebellar CMs with or without associated DVAs in our hospital to analyze the clinical and radiological characteristics of CCMs and to assess the various therapeutic strategies.
Between February 2009 and April 2012, 456 consecutive patients (236 male and 220 female) harboring CMs involving the brain were hospitalized and treated at the Beijing Tiantan Hospital of Capital Medical University. Of these patients, 41 were diagnosed with CCMs. These CCM patients accounted for 8.99% of all of the brain CM patients. We excluded all of the supratentorial cases, all of the patients with CMs that were localized primarily in the brainstem and extended to the cerebellum, and all of the patients with CMs that were located at the cerebellopontine angle (CPA) and tentorium. The clinical data, including the patient’s age, sex, medical history, clinical presentation, radiological studies, and surgical notes, were reviewed and characterized. The study was approved by the Beijing Tiantan Hospital Review Committee. The patient information is summarized in Additional file 1: Table S1.
Each patient's clinical presentation was classified as incidental/asymptomatic or symptomatic hemorrhage (headache, vertigo, vomiting, gait disturbance, and ataxia). The diagnosis of symptomatic hemorrhage was made if there was a clinical history of acute neurological deterioration and either magnetic resonance imaging (MRI) or computed tomography (CT) evidence of associated acute hemorrhage.
The diagnosis of CM was established by MRI in 41 cases and by histopathological confirmation in 38 cases (36 cases of CCMs, one brain stem CM, and one temple CM). The diagnosis of CMs with or without associated DVAs was defined by MRI (41 cases) and/or by digital subtraction angiography (DSA) (9 cases) and subsequently confirmed by surgical findings (36 cases). MRI or DSA was used to define CMs and DVAs as per published criteria [19, 20].
The size of the CM was measured using serial MRI or CT and/or intraoperative measurement.
A CM was considered for surgical treatment if at least one of the necessary criteria described by Porter were fulfilled . In total, 36 patients underwent surgery for the removal of CCMs. In addition, one of the two patients with multiple CMs underwent resection of a temple CM, and the other underwent resection of a brain stem CM. The other three patients were treated conservatively.
The morbidity and mortality were recorded. Any newly emerging neurological dysfunction or deterioration of a prior neurological deficit that appeared shortly after operation (within one week) was defined as a bad short-term result. No new neurological dysfunction or mitigation of an original neurological deficit after surgery was regarded as a good short-term result.
The most recent checkup was conducted in October 2012. The modified Rankin Scale (mRS)  was used to grade the long-term outcomes: mRS scores of 3–6 referred to bad long-term outcomes, and mRS scores of 0–2 referred to good long-term outcomes.
The statistical comparisons were performed using Fisher's exact test for category variables or one-way ANOVA (analysis of variance) for continuous variables. All of the statistical analyses were performed using the SPSS 18.0 software (SPSS, Inc. Chicago, IL, USA). Differences with a P-value of less than 0.05 were considered statistically significant.
Characteristics of the included population and comparison between CCMs with and without associated DVAs
Comparison between patients diagnosed with CCMs with and without associated DVAs (Fisher’s exact test)
CCMs + DVA
Initial clinical presentation
Location of CM
Cerebellar hemisphere + Vermis
Multiplicity of CMs
Comparison between patients diagnosed with CCMs with and without associated DVAs (one-way ANOVA)
CCMs + DVA
Mean maximum lesion diameter (cm)
Patterns of relationship between CCMs and associated DVAs
In the 11 cases analyzed in this study, the distal radicles of the DVAs usually covered the anterior aspect, the top of the CCMs. In no case did the distal radicles of the DVAs cover the bottom aspect of the CMs, and the trunk of the DVAs never extended downward.
The clinical follow-up period ranged from 6 months to 42 months (38 patients; mean 22.3 months), and the radiographic follow-up (MRI and/or CT) period ranged from 6 months to 41 months (38 patients; mean 17.7 months). Of the 36 surgical patients, 33 attended the follow-up, two were lost, and one died from an accident. All of the patients in both the CM and the CM + DVA groups had good long-term prognosis, and there was no statistically significant difference between the two groups (Table 2). No CCM reoccurrence or rehemorrhage was observed in the 33 patients. Of the five conservatively treated CCM patients, one patient (patient 1) suffered a cerebellar lesion and minor enlargement, and we have continued to observe the patient’s progress.
Intracranial vascular malformations were originally classified by McCormick  into five types: telangiectasias, varix, cavernous malformation, arteriovenous malformation, and venous malformation. The definition of each of these types of malformations depends on distinct pathological criteria. However, mixed or transitional vascular malformations with the pathological features of more than one type of malformation within the same lesion have been recently described. The detection of a wide spectrum of intermediate forms of McCormick’s original categories suggests that these lesions might be a continuum of progression from a single pathological process . The coexistence of a CM and a DVA is the most common presentation of a mixed vascular malformation. Much discrepancy exists in the literature concerning the prevalence of coexisting CMs and DVAs . Based on findings from MR imaging studies, Abdulrauf  found that 13 (24%) of 55 patients with supratentorial and infratentorial CMs also had associated DVAs. A similar percentage was reported by Wurm , who found this type of association in 15 (25.9%) of 58 patients with cerebral, cerebellar, and brain stem CMs based on MR imaging and intraoperative findings. In 86 surgically treated patients with brainstem CMs, Porter  found a DVA that was intimately associated with each resected CM. Oliveira  reported cerebellar CMs in 10 cases, but none of these were associated with a DVA. In our study, 11 cerebellar CMs (26.8%) with associated DVAs were identified in 41 consecutive cerebellar CM patients.
Abdulrauf  compared the clinical profile of patients harboring CMs with and without associated DVAs. Compared with patients with CMs alone, patients with CMs associated with DVAs are more likely to be female, have associated symptomatic hemorrhage, have lesions in the posterior fossa (statistically significant), and suffer from repeated symptomatic hemorrhage and are less likely to present with seizures or to have familial histories. The authors of several reports have suggested that the CMs associated with a DVA have a more aggressive clinical course than CMs alone [11, 14, 15, 23]. In our study, the CCMs associated with DVAs did not present a more aggressive nature. There were no statistically significant differences between the patients with CCMs with and without DVAs regarding age, sex, location and size of the lesions, and initial clinical presentation. Five of the 30 patients (16.7%) in the CM group and none of the 11 patients (0%) in the CM + DVA group had multiple CMs (P = 0.30, not statistically significant). Familial cerebral CMs caused by loss-of-function mutations are often characterized by multiple lesions . If substantiated in a larger case series, this difference of multiplicity may suggest different pathogenesis mechanisms (i.e., genetic factors, structural venous outflow factors, and hemodynamic variables) of the host’s predisposition to CCMs with and without associated DVAs.
The association of CMs and DVAs within the same lesion has generated hypotheses about the causation–evolution relationship among different types of malformations. It has been postulated that the abnormal hemodynamics of DVAs might induce the formation of CMs . It has also been suggested that chronically increased intraluminal pressure and the resulting reduced tissue perfusion leading to tissue hypoxia may stimulate a local increase in angiogenic factors, which would induce the formation of vascular malformations . If there are mixed vascular malformations in a region, DVAs can be considered the primary congenital lesion, and venous hypertension can be regarded as the initial pathophysiological factor leading to the formation of CMs [14, 17, 18, 25].
At the same time, DVAs are also responsible for the venous drainage of otherwise normal brain tissue. The removal of the whole DVA to prevent the reoccurrence of the associated CM could result in venous engorgement and cerebral edema, which might have devastating consequences. As a result, the following treatment protocol is recommended for patients with CMs associated with DVAs to avoid the risk of venous infarction: microsurgical resection of the CM alone and an “untouching” strategy for the DVA [4, 10, 16].
These two vascular malformations are usually connected by small medullary veins. The concurrent CM is located in the territory of the DVA, and the DVA’s distal radicles are part of the CM. The untouching of the DVA is difficult and even unrealistic unless residual CM is left in the region, which might result in CM reoccurrence and rehemorrhage.
The authors of some surgical reports have challenged this prevalent thinking and have described a significantly improved operative treatment of DVAs . In a recent provocative report, Wurm  proposed the coagulation and division of the transcerebral vein of the DVAs to prevent CM recurrence. In their series of 15 patients with DVAs and CMs, these researchers removed the CM and divided the transcerebral vein of the DVA in nine of the patients: in six during the first operation and in the remaining three patients after recurrence of the associated CM with symptomatic hemorrhage. These authors observed no brain swelling intraoperatively, and the postoperative course was uneventful in all of these nine patients. Their experience supports the theory that the abnormal draining vein might be the actual pathological lesion that causes blood flow disturbances with recurrent and newly developing malformations. Coagulation of the large transcerebral draining vein did not lead to any ischemic or hemorrhagic infarction or any other complication.
The four patterns of relationship between CCMs and associated DVAs found in our study were summarized. The distal branches of the DVAs always covered the anterior top aspects of the CM, and the trunk of the DVA is more likely to extend upward and forward. In no cases did the distal radicles of the DVA cover the bottom aspect of the CM, and the trunk of the DVA never extended downward. In most surgical cases, the cerebellum is exposed from the back and lower head; thus, the relationship patterns of the CCMs and associated DVAs provide the surgeon great convenience to reach the CM and to coagulate and dissect the connected radicles without the barrier of the trunk. This surgical strategy might markedly aid the safe and radical removal of CMs and prevent the reoccurrence of CMs, and these patients may also have good long-term prognosis. It has to be emphasized that the surgeon must be alert when completing the resection of the CM because the trunk of the DVA is usually hidden behind the CM. In two of the patients analyzed in our study, the trunks of the DVAs might have been injured during the dissection of the anterior aspect and top aspect of the CMs, which would cause serious and dangerous cerebellar edema.
In our series, the results preliminarily showed similarity in the clinical characteristics and surgical prognosis between CCMs associated or not associated with DVAs. A more definitive conclusion would require a larger sample size, randomized clinical trial, and a longer prospective follow-up. In addition, it must be noted that the postoperative incidence of early serious cerebellar edema in the CCMs with associated DVAs in our series was much higher than that obtained with the pure CCM cases (20% vs. 0%), but this different was not statistically significant. Further research is necessary to determine whether the operation of CCMs with associated DVAs is associated with higher early morbidity.
It is not rare that associated DVAs are found in CCM cases. There were no statistically significant differences between the patients with pure CCMs and the patients with CCMs with associated DVAs with respect to age, sex, location and size of lesions, multiplicity, initial clinical presentation, frequency of symptomatic hemorrhage, preoperative mRS, and surgical prognosis. The total removal of the CCM combined with the coagulation and dissection of the distal radicles at the length of the associated CM and the preservation of the trunk of the developmental venous anomalies can result in good long-term prognosis in patients.
Written informed consent was obtained from the patient for the publication of this report and any accompanying images.
The authors would like to thank Dr. Jun Wu for the useful discussions. This study was supported by a “National Science and Technology Support Program (No. 2011BAI08B08)” grant (Principal Investigator, Professor Shuo Wang) from the Ministry of Health of China.
- Del Curling O, Jr KDL, Elster AD, Craven TE: An analysis of the natural history of cavernous angiomas. J Neurosurg. 1991, 75: 702-708. 10.3171/jns.1991.75.5.0702.View ArticlePubMedGoogle Scholar
- Kim DS, Park YG, Choi JU, Chung SS, Lee KC: An analysis of the natural history of cavernous malformations. Surg Neurol. 1997, 48: 9-18. 10.1016/S0090-3019(96)00425-9.View ArticlePubMedGoogle Scholar
- Moriarity JL, Wetzel M, Clatterbuck RE, Javedan S, Sheppard JM, Hoenig-Rigamonti K, Crone NE, Breiter SN, Lee RR, Rigamonti D: The natural history of cavernous malformations: a prospective study of 68 patients. Neurosurg. 1999, 44: 1166-1173.Google Scholar
- Porter RW, Detwiler PW, Spetzler RF, Lawton MT, Baskin JJ, Derksen PT, Zabramski JM: Cavernous malformations of the brainstem: experience with 100 patients. J Neurosurg. 1999, 90: 50-58. 10.3171/jns.1999.90.1.0050.View ArticlePubMedGoogle Scholar
- Robinson JR, Awad IA, Little JR: Natural history of the cavernous angioma. J Neurosurg. 1991, 75: 709-714. 10.3171/jns.1991.75.5.0709.View ArticlePubMedGoogle Scholar
- Bertalanffy H, Benes L, Miyazawa T, Alberti O, Siegel AM, Sure U: Cerebral cavernomas in the adult. Review of the literature and analysis of 72 surgically treated patients. Neurosurg Rev. 2002, 25: 1-55. 10.1007/s101430100179.View ArticlePubMedGoogle Scholar
- de Oliveira JG, Rassi-Neto A, Ferraz FA, Braga FM: Neurosurgical management of cerebellar cavernous malformations. Neurosurg Focus. 2006, 15: e11-Google Scholar
- Hasegawa T, McInerney J, Kondziolka D, Lee JY, Flickinger JC, Lunsford LD: Long-term results after stereotactic radiosurgery for patients with cavernous malformations. Neurosurg. 2002, 50: 1190-1198.Google Scholar
- Mori K, Seike M, Kurisaka M, Kamimura Y, Morimoto M: Venous malformation in the posterior fossa: guidelines for treatment. Acta Neurochir (Wien). 1994, 126: 107-112. 10.1007/BF01476418.View ArticleGoogle Scholar
- Rigamonti D, Spetzler RF: The association of venous and cavernous malformations. Report of four cases and discussion of the pathophysiological, diagnostic, and therapeutic implications. Acta Neurochir (Wien). 1988, 92: 100-105. 10.1007/BF01401979.View ArticleGoogle Scholar
- Abdulrauf SI, Kaynar MY, Awad IA: A comparison of the clinical profile of cavernous malformations with and without associated venous malformations. Neurosurg. 1999, 44: 41-47. 10.1097/00006123-199901000-00020.View ArticleGoogle Scholar
- Perrini P, Lanzino G: The association of venous developmental anomalies and cavernous malformations: pathophysiological, diagnostic, and surgical considerations. Neurosurg Focus. 2006, 15: e5-Google Scholar
- Töpper R, Jürgens E, Reul J, Thron A: Clinical significance of intracranial developmental venous anomalies. J Neurol Neurosurg Psychiatry. 1999, 67: 234-238. 10.1136/jnnp.67.2.234.View ArticlePubMedPubMed CentralGoogle Scholar
- Awad IA, Robinson JR, Mohanty S, Estes ML: Mixed vascular malformations of the brain: clinical and pathogenetic considerations. Neurosurg. 1993, 33: 179-188. 10.1227/00006123-199308000-00001.View ArticleGoogle Scholar
- Ciricillo SF, Dillon WP, Fink ME, Edwards MS: Progression of multiple cryptic vascular malformations associated with anomalous venous drainage. Case report. J Neurosurg. 1994, 81: 477-481. 10.3171/jns.1994.81.3.0477.View ArticlePubMedGoogle Scholar
- Rigamonti D, Spetzler RF, Medina M, Rigamonti K, Geckle DS, Pappas C: Cerebral venous malformations. J Neurosurg. 1990, 73: 560-564. 10.3171/jns.1990.73.4.0560.View ArticlePubMedGoogle Scholar
- Wilson CB: Cryptic vascular malformations. Clin Neurosurg. 1992, 38: 49-84.PubMedGoogle Scholar
- Wurm G, Schnizer M, Fellner FA: Cerebral cavernous malformations associated with venous anomalies: surgical considerations. Neurosurg. 2005, 57: S42-S58.View ArticleGoogle Scholar
- Garner TB, Del Curling O, Jr KDL, Laster DW: The natural history of intracranial venous angiomas. J Neurosurg. 1991, 75: 715-722. 10.3171/jns.1991.75.5.0715.View ArticlePubMedGoogle Scholar
- Sigal R, Krief O, Houtteville JP, Halimi P, Doyon D, Pariente D: Occult cerebrovascular malformations: Follow-up with MR imaging. Radiol. 1990, 176: 815-819.View ArticleGoogle Scholar
- van Swieten JC, Koudstaal PJ, Visser MC, Schouten HJ, van Gijn J: Interobserver agreement for the assessment of handicap in stroke patients. Stroke. 1998, 19: 604-607.View ArticleGoogle Scholar
- McCormick WF: The pathology of vascular (“arteriovenous”) malformations. J Neurosurg. 1966, 24: 807-816. 10.3171/jns.1966.24.4.0807.View ArticlePubMedGoogle Scholar
- Kamezawa T, Hamada JI, Niiro M, Kai Y, Ishimaru K, Kuratsu JI: Clinical implications of associated venous drainage in patients with cavernous malformation. J Neurosurg. 2005, 102: 24-28. 10.3171/jns.2005.102.1.0024.View ArticlePubMedGoogle Scholar
- Kattapong VJ, Hart BL, Davis LE: Familial cerebral cavernous angiomas: clinical and radiologic studies. Neurol. 1995, 45: 492-497. 10.1212/WNL.45.3.492.View ArticleGoogle Scholar
- Hong YJ, Chung TS, Suh SH, Park CH, Tomar G, Seo KD, Kim KS, Park IK: The angioarchitectural factors of the cerebral developmental venous anomaly; can they be the causes of concurrent sporadic cavernous malformation?. Neuroradiology. 2010, 52: 883-91. 10.1007/s00234-009-0640-6.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2377/13/134/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.