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Late complications of radiosurgery for cerebral arteriovenous malformations: report of 5 cases of chronic encapsulated intracerebral hematomas and review of the literature



Chronic encapsulated intracerebral hematomas (CEIHs) are a rare, late complication of radiosurgery for intracranial AVM. We present 5 cases treated mostly by surgical excision and review the literature.


Patients (age 39, 42, 36, 31, 62) presented with headache, paresthesia, hemiparesis or were asymptomatic. CEIHs presented 10 to 13 years (median 12 years) post radiosurgery. Three patients had demonstrated early radiation induced changes post radiosurgery. Angiographic cure, assessed with DSA, was present in all cases except 1 case with a small nidus remnant. MRI demonstrated mixed lesions with a solid enhancing part, organized hematoma and extensive surrounding edema while three cases had also a cystic component.


Excision of the CEIHs with complete or partial removal of the capsule was performed in 4 patients and resulted in marked clinical improvement. One patient was managed conservatively with administration of steroids as surgery was judged excessively hazardous with eventual stabilization of his symptoms.


CEIHs are rare, late complications of radiosurgery for cranial AVM. They may be asymptomatic or provoke symptoms and may be preceded by early radiation induced changes. Complete removal of CEIHS is an effective treatment. Because of the long latency period of CEIHs, patients who had radiosurgery for brain AVMs should be followed by MRI at least 10 years even after complete obliteration.

Stereotactic radiosurgery (SRS) has become an alternative or complementary treatment for brain arteriovenous malformations (AVMs) especially for lesions that are small (< 3 cm), large and complex, or located in eloquent areas [1, 2]. Delayed complications post bAVM SRS are rare, typically detected 5 or more years after SRS. They include cyst formation, de novo cavernoma formation and chronic encapsulated intracerebral hematoma (CEIH) [3,4,5,6,7,8]. They are distinct from radiation-induced changes (RICs) noted in the first 1 to 2 years after AVM SRS (areas of increased T2 signal) and radionecrosis [9,10,11,12,13]. Delayed complications can cause mass effect and, if symptomatic, may require surgical intervention [14].

We report 5 cases of CEIH that developed in patients with bAVMs that had been completely obliterated using SRS and review the literature.

Materials and methods

The Neurointerventional Department of the University of Nancy, Nancy, France, is a tertiary center serving a region of 2,35 million inhabitants. We reviewed our medical records for the period 1997 to 2014 during which 288 patients were treated with radiosurgery for a brain arteriovenous malformation. We obtained the presentation, diagnosis, management and clinical outcomes of 5 cases of interest. Because of the retrospective nature of the study, permission from the ethics committee of our institution was not necessary. This research complies with the STROBE (Strengthening the Reporting of Observational studies in Epidemiology) reporting guidelines. We also performed a comprehensive literature search using Pubmed. The following key words were queried singly and in combination: arteriovenous malformation, brain, hematoma, radiosurgery. Our search resulted in case reports and cases series describing CEIH post bAVM SRS. In all cases that could be extracted (including ours and the cases in the referenced articles), we collected the clinical presentations, imaging findings, management and outcome.

Illustrative cases

Three of the 5 patients were males. The mean patient age was 30,8 years (range 27 to 49 years). The presenting symptom was seizures in 3 cases and hemorrhage in 2 cases. AVMs were located in the temporal lobe in 2 cases, and the parietal, frontal and occipital lobes in the other cases. All lesions were partially embolized prior to radiosurgery. The marginal dose delivered was 18 Grays for all lesions. The mean irradiated nidus volume was 5,2 ml (range 3,8 to 9 ml). Four of five AVMs were angiographically obliterated post radiosurgery. Three cases demonstrated RICs following radiosurgery. The mean time of CEIH presentation was 10,2 years post radiosurgery (range 6 to 13 years). MRI studies showed hemorrhagic lesions with extensive peri-lesional edema (Fig. 1). A cyst coexisted with the hemorrhagic lesion in 3 cases (Fig. 2). Three cases were immediately treated with surgical excision of the hemorrhagic lesion and the cystic component. Two cases were treated conservatively with steroid administration. One of these cases showed interval growth and symptom worsening after 2 years and was eventually treated surgically while the other case remained clinically stable during a follow-up period of 8 years (Fig. 3). All surgically treated cases demonstrated typical histological features of CEIH and clinical improvement.

Fig. 1

Case 1. A 27-year-old woman presented with hemorrhage due to a left temporal AVM. After partial treatment with embolization, 18 Grays were delivered to the margin of the lesion with a collimator of 20 mm. Twelve years post SRS the patient complained of chronic headache. a Axial Flair and (b) axial T1 contrast enhanced images showed a large heterogeneous well delineated cavernoma-like lesion. Surgery was initially recused because of the deep location and the mild symptoms of the patient. b Axial Flair, c axial T2* MRI images 2 years later showed lesion growth which was surgically removed. d Histology revealed an angiomatous pseudo-cavernous lesion containing dilated vascular lumen, fibrino-hemorraghic changes and fibrosis (hematoxylin, eosin and saffron, × 100)

Fig. 2

Case 4. A 21-year-old man presented with seizures related to a left temporal AVM. The lesion was partially treated with embolization. A nidal remnant was further treated with 18 Grays delivered at the periphery of a target volume of 5,3 ml. Two years post SRS an MRI showed mild radiation induced changes. Ten years post SRS, the patient presented with headache and paresthesia. a axial Flair at the time of SRS. Axial Flair (b) and (c) SWI 11 years later show a large cystic lesion with chronic hemorrhage and an enhancing nodular part with surrounding edema. The cyst was evacuated, and the walls partially removed. Histology showed (d) a well-circumscribed vascular lesion with extensive fibrosis (hematoxylin, eosin and saffron, × 40) and (e) post radiation hyalinization of small vessels (hematoxylin, eosin and saffron, × 400)

Fig. 3

Case 5. A 49-year-old man presented with intracranial hemorrhage related to a right occipital AVM. The lesion was partially treated with embolization. A nidal remnant was further treated with SRS with a marginal dose of 18 Grays. Thirteen years post SRS, the patient presented hemiparesis. a Flair, (b) T2*, (c) T1 and d) T1 contrast enhanced MR images show a large heterogeneous cavernoma-like lesion with extensive edema. Surgery was judged as too risky and the lesion finally stabilized under steroid therapy

Literature search

We found 32 cases of CEIH in case reports and case series. Reports with insufficient or no data were excluded. In total, 37 cases including our own 5 cases were analyzed (Table 1).

Table 1 Reported cases of CEIHs


In the 37 cases analyzed, the mean age was 33,7 years (sd 15,3 years) with a 1:1.2 male to female predominance. The characteristics of these patients are depicted in Table 1. Forty four percent of AVMs had initially bled. The nidus was located in the cerebral lobes in 69%, in the basal ganglia in 27,5% and in the cerebellum in 1 (3,4%) patient. Previous embolizations had been performed in 39,3% of patients. Radiation was delivered by gamma knife radiosurgery in 74,3% cases while the rest were treated with a linear accelerator. Six cases were irradiated 2 times and 1 case three times. The marginal dose had a mean of 20,3 Grays, sd 3,1 Grays. Before the development of CEIHs, RICs or radionecrosis in the years post radiosurgery had been observed in 32,4% patients. Expanding intracerebral hematomas were discovered after a mean of 7,7 years (sd 3,7 years) post SRS. On T2-weight imaging, CEIHs manifested as heterogeneous lesions in 54,1%, low intensity lesion in 20,8%, had a hypointense rim in 54,1%, and had nodular or modular enhancement on T1-weighted contrast enhanced in 45,8% of cases. A cystic component coexisting with the CEIH was observed in 62,1% of patients. Symptoms ranged from headache (44,8%), hemiparesis (41,3%), nausea/vomiting (13,7%), asymptomatic (10,3%), paresthesia (6,8%), visual disturbances (6,8%), ataxia (3,4%), seizures (3,4%), memory disturbances (3,4%) and facial palsy (3,4%). Angiographic obliteration of the cerebral AVM had been achieved in 78,3% of CEIHs.

Data on the therapeutic management were available in 35 patients. Complete excision was performed in 10 cases and led to clinical and/or radiological improvement in 9 patients, while 1 remained stable. Three cases were treated with partial excision with good results. Four patients had only the cystic component treated (2 patients with Omaya reservoir placement and 2 patients with evacuation). However, this approach failed to provide clinical improvement in 3 patients who eventually underwent complete excision with good results.

Follow-up or medical management with steroids was attempted in 18 patients of whom 16 eventually underwent excision and 1 partial excision because of lesion enlargement or non-improving symptoms. In this group, improvement was reported in 9 patient, 1 patient with partial excision experienced worsening while 7 patients were lost to follow-up. Surgery was judged hazardous in one patient (patient 5 in the present series) who remained clinically stable at 8 years follow-up.


Chronic encapsulated intracerebral hematomas are a very rare complication of radiosurgery for cerebral AVM. The incidence in our cohort of treated patients was 1,8% of patients with brain AVM treated with SRS over a period of 17 years. Other series attest to the rarity of this complication with reported incidences ranging from 0,6 to 4% [1, 16, 24, 25]. However, the long latency period of CEIHs and the cessation of imaging controls once nidus obliteration has been documented may have led to the underestimation of the true prevalence [26]. Longer periods of imaging follow-up, at least years post radiosurgery have been suggested [19].

Histologically CEIHs are made of a thickened hematoma capsule with abundant microvasculature that can easily bleed when removed surgically. The hematoma itself is serous and is usually easily aspirated. The gross appearance is similar to chronic subdural hematoma. CEIHs may develop near vascular lesions such as AVMs, cavernous angiomas and venous angiomas. It is thought that CEIHs develop secondary to hemorrhagic episodes of the initial angiomatous lesion with its eventual “self-destruction” or thrombosis [4, 16, 27, 28]. In the case of post radiosurgery obliterated AVMs, it is thought that radiation-induced inflammation triggers neo-angiogenesis of fragile new vessels, breakdown of the blood-brain barrier, fluid exudation in the nearby brain, edema and potential cyst formation. Dense vascularization has been found in the capsule of CEIHs and it is thought that bleeding of these fragile vessels results in expansion of the capsule and further bleeding, a mechanism similar to chronic subdural hematoma [23, 29,30,31]. Neovascularization and hematoma expansion appear to be mediated by VEGF (Vascular Permeability Factor), a potent vascular endothelial cell mitogen that promotes neovascularization and vascular permeability [22] associated also to chronic subdural hematoma pathophysiology. Further studies are needed to elucidate the mechanisms of CEIHs post AVM radiosurgery.

On MR imaging, a common finding in all cases of CEIHs was extensive perilesional edema. Most cases demonstrated as low intensity or heterogeneous lesions on T2 weighted imaging with or without a hypodense rim. On contrast enhanced T1 weighted images there existed usually nodular or multinodular enhancement (Table 1). CEIHs were associated with cyst in 62,1% of cases pointing to a possible common pathophysiologic mechanism [3]. The latency time from radiosurgery to CEIHs diagnosis was 7,7 years sd 3,7 years. Symptoms, the most common being from headache (44,8%), hemiparesis (41,3%), nausea/vomiting (13,7%) were mostly related to the mass effect of the gradually growing CEIH and the surrounding edema.

Several risk factors have been explored for the development of CEIHs including age, sex, basal ganglia AVM location, irradiated nidus volume, the marginal or total dose, early RICs, repeat radiosurgery, nidus obliteration, pre-radiosurgery embolization, pre-radiosurgery surgery and prior hemorrhage with inconsistent results [16, 25, 26, 28, 32]. In the present review, the distributions of age, sex, location, marginal dose, nidus obliteration and pre-radiosurgery embolization did not differ from distributions seen in cohorts of AVMs treated by radiosurgery. However, the incidence of radiation induced changes in the years post radiosurgery was unusually high (32,4%). There was also a high percentage (18,9%) of cases which had received repeat radiosurgery. Further studies are needed to ascertain the risk factors and mechanisms of CEIHs that develop post SRS for AVM [14].

CEIHs often caused progressive neurological deficits due to mass effect. The most efficient treatment was complete excision that led to clinical and/or radiological improvement in cases. Partial treatment was less efficient and had to be complemented by complete excision in cases. Conservative management consisting of follow-up or steroid administration was unsuccessful in most cases and had to be complemented by total excision of the hematoma and the capsule to achieve good clinical outcome.

This study is susceptible to a number of biases inherent to any retrospective study and review like the small number of cases, selection bias and publication bias. The time CEIHs were detected was mostly based on the timing of symptom development and asymptomatic CEIHs may have been underreported. Larger studies are needed to further elucidate the pathophysiology, incidence and risk factors related to the development of CEIHs post cerebral AVM radiosurgery.


CEIHs are a rare late complication that develop after SRS to treat cerebral AVMs. A potential risk factor is the appearance of radiation induced changes post SRS. CEHIs become usually symptomatic because of their mass effect and extensive surrounding edema. To manage these symptoms, CEIHs should ideally be evacuated with complete capsule removal. Partial capsule removal in the case of lesions in eloquent regions may be an alternative treatment.

Availability of data and materials

The datasets during and/or analysed during the current study are available from the corresponding author on reasonable request.



Stereotactic Radiosurgery


Brain Arteriovenous Malformation


Chronic Encapsulated Intracerebral Hematoma


Radiation-induced change


Strengthening the Reporting of Observational studies in Epidemiology


Vascular Permeability Factor


  1. 1.

    Takeuchi S, Takasato Y, Masaoka H, et al. Development of chronic encapsulated intracerebral hematoma after radiosurgery for a cerebral arteriovenous malformation. Acta Neurochir. 2009;151:1513–5.

    Article  Google Scholar 

  2. 2.

    Huo X, Jiang Y, Lv X, et al. Gamma knife surgical treatment for partially embolized cerebral arteriovenous malformations. J Neurosurg. 2016;124:767–76.

    Article  Google Scholar 

  3. 3.

    Shuto T, Ohtake M, Matsunaga S. Proposed mechanism for cyst formation and enlargement following gamma knife surgery for arteriovenous malformations. J Neurosurg. 2012;117(Suppl):135–43.

    Article  Google Scholar 

  4. 4.

    Foroughi M, Kemeny AA, Lehecka M, et al. Operative intervention for delayed symptomatic radionecrotic masses developing following stereotactic radiosurgery for cerebral arteriovenous malformations--case analysis and literature review. Acta Neurochir. 2010;152:803–15.

    Article  Google Scholar 

  5. 5.

    Schaller C, Liefner M, Ansari S, et al. Operation for delayed symptomatic brain oedema after treatment of an arteriovenous malformation by embolization and radiosurgery. Acta Neurochir. 2005;147:1103–8 discussion 1108.

    CAS  Article  Google Scholar 

  6. 6.

    Radanowicz-Harttmann V, Bachli H, Gratzl O. Late complication of radiosurgery of AVMs with the gamma knife: a case report. Acta Neurochir. 1998;140:194–5.

    CAS  Article  Google Scholar 

  7. 7.

    Kurita H, Sasaki T, Kawamoto S, et al. Chronic encapsulated expanding hematoma in association with gamma knife stereotactic radiosurgery for a cerebral arteriovenous malformation. Case report. J Neurosurg. 1996;84:874–8.

    CAS  Article  Google Scholar 

  8. 8.

    Motegi H, Kuroda S, Ishii N, et al. De novo formation of cavernoma after radiosurgery for adult cerebral arteriovenous malformation--case report. Neurol Med Chir (Tokyo). 2008;48:397–400.

    Article  Google Scholar 

  9. 9.

    Flickinger JC, Kondziolka D, Lunsford LD, et al. Development of a model to predict permanent symptomatic postradiosurgery injury for arteriovenous malformation patients. Arteriovenous malformation radiosurgery study group. Int J Radiat Oncol Biol Phys. 2000;46:1143–8.

    CAS  Article  Google Scholar 

  10. 10.

    Lax I, Karlsson B. Prediction of complications in gamma knife radiosurgery of arteriovenous malformation. Acta Oncol. 1996;35:49–55.

    CAS  Article  Google Scholar 

  11. 11.

    Voges J, Treuer H, Lehrke R, et al. Risk analysis of LINAC radiosurgery in patients with arteriovenous malformation (AVM). Acta Neurochir Suppl. 1997;68:118–23.

    CAS  PubMed  Google Scholar 

  12. 12.

    Han JH, Kim DG, Chung H-T, et al. Clinical and neuroimaging outcome of cerebral arteriovenous malformations after gamma knife surgery: analysis of the radiation injury rate depending on the arteriovenous malformation volume. J Neurosurg. 2008;109:191–8.

    Article  Google Scholar 

  13. 13.

    Yen C-P, Matsumoto JA, Wintermark M, et al. Radiation-induced imaging changes following gamma knife surgery for cerebral arteriovenous malformations. J Neurosurg. 2013;118:63–73.

    Article  Google Scholar 

  14. 14.

    Park JC, Ahn JS, Kwon DH, et al. Growing organized hematomas following gamma knife radiosurgery for cerebral Arteriovenous malformation : five cases of surgical excision. J Korean Neurosurg Soc. 2015;58:83.

    CAS  Article  Google Scholar 

  15. 15.

    Maruyama K, Shin M, Tago M, Kurita H, Kawahara N, Morita A, et al. Management and outcome of hemorrhage after Gamma Knife surgery for arteriovenous malformations of the brain. J Neurosurg. 2006;105Suppl:52–7.

  16. 16.

    Pan DH-C, Kuo Y-H, Guo W-Y, et al. Gamma knife surgery for cerebral arteriovenous malformations in children: a 13-year experience. J Neurosurg Pediatr. 2008;1:296–304.

    Article  Google Scholar 

  17. 17.

    Nakamizo A, Suzuki SO, Saito N, Shono T, Matsumoto K, Onaka S, et al. Clinicopathological study on chronic encapsulated expanding hematoma associated with incompletely obliterated AVM after stereotactic radiosurgery. Acta Neurochir (Wien). 2011;153(4):883–93.

    Article  Google Scholar 

  18. 18.

    Lee C-C, Pan DH-C, Ho DM-T, Wu H-M, Chung W-Y, Liu K-D, et al. Chronic encapsulated expanding hematoma after gamma knife stereotactic radiosurgery for cerebral arteriovenous malformation. Clin Neurol Neurosurg. 2011;113(8):668–71.

    Article  Google Scholar 

  19. 19.

    Takeuchi S, Takasato Y, Masaoka H. Chronic encapsulated intracerebral hematoma formation after radiosurgery for cerebral arteriovenous malformation. Neurol India. 2011;59:624–6.

    Article  Google Scholar 

  20. 20.

    Watanabe T, Nagamine H, Ishiuchi S. Progression of cerebellar chronic encapsulated expanding hematoma during late pregnancy after gamma knife radiosurgery for arteriovenous malformation. Surg Neurol Int. 2014;5(Suppl 16):S575–9.

    Article  Google Scholar 

  21. 21.

    Shuto T, Yagishita S, Matsunaga S. Pathological characteristics of cyst formation following gamma knife surgery for arteriovenous malformation. Acta Neurochir (Wien). 2015;157(2):293–8.

    Article  Google Scholar 

  22. 22.

    Takei J, Tanaka T, Yamamoto Y, et al. Chronic encapsulated expanding thalamic hematoma associated with obstructive hydrocephalus following radiosurgery for a cerebral Arteriovenous malformation: a case report and literature review. Case Rep Neurol Med. 2016;2016:5130820.

    PubMed  Google Scholar 

  23. 23.

    D’Aliberti GA, Colistra D, Iacopino G, et al. Hydrocephalus due to a cavernoma-like lesion of an obliterated cerebral arteriovenous malformation treated by embolization and radiosurgery. World Neurosurg.

  24. 24.

    Hasegawa T, Kato T, Naito T, et al. Long-term outcomes for pediatric patients with brain arteriovenous malformations treated with gamma knife radiosurgery, part 2: the incidence of cyst formation, encapsulated hematoma, and radiation-induced tumor. World Neurosurg.

  25. 25.

    Nakajima H, Yamanaka K, Ishibashi K, et al. Delayed cyst formations and/or expanding hematomas developing after gamma knife surgery for cerebral arteriovenous malformations. J Clin Neurosci. 2016;33:96–9.

    Article  Google Scholar 

  26. 26.

    Pollock BE, Link MJ, Branda ME, et al. Incidence and Management of Late Adverse Radiation Effects after Arteriovenous Malformation Radiosurgery. Neurosurgery. 2017;81:928–34.

    Article  Google Scholar 

  27. 27.

    Pollock BE, Brown RDJ. Management of cysts arising after radiosurgery to treat intracranial arteriovenous malformations. Neurosurgery. 2001;49:255–9.

    Google Scholar 

  28. 28.

    Izawa M, Hayashi M, Chernov M, et al. Long-term complications after gamma knife surgery for arteriovenous malformations. J Neurosurg. 2005;102(Suppl):34–7.

    Article  Google Scholar 

  29. 29.

    Hohenstein A, Erber R, Schilling L, et al. Increased mRNA expression of VEGF within the hematoma and imbalance of angiopoietin-1 and -2 mRNA within the neomembranes of chronic subdural hematoma. J Neurotrauma. 2005;22:518–28.

    Article  Google Scholar 

  30. 30.

    Dvorak AM, Kohn S, Morgan ES, et al. The vesiculo-vacuolar organelle (VVO): a distinct endothelial cell structure that provides a transcellular pathway for macromolecular extravasation. J Leukoc Biol. 1996;59:100–15.

    CAS  Article  Google Scholar 

  31. 31.

    Dvorak HF, Brown LF, Detmar M, et al. Vascular permeability factor/vascular endothelial growth factor, microvascular hyperpermeability, and angiogenesis. Am J Pathol. 1995;146:1029–39.

    CAS  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Takeuchi S, Wada K, Sakakibara F, et al. Chronic encapsulated intracerebral hematoma associated with cavernous malformation. J Korean Neurosurg Soc. 2014;55:89–91.

    Article  Google Scholar 

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Authors declare not to have received any type of funding for the present work.

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S.F. analyzed the data and prepared the manuscript, R.A., V.B., I.B., O.K., S.B., gathered the data, read and approved the final manuscript.

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Correspondence to Stephanos Finitsis.

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Finitsis, S., Bernier, V., Buccheit, I. et al. Late complications of radiosurgery for cerebral arteriovenous malformations: report of 5 cases of chronic encapsulated intracerebral hematomas and review of the literature. Radiat Oncol 15, 177 (2020).

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