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Research ArticleAdult Brain
Open Access

Baseline and Evolutionary Radiologic Features in Sporadic, Hemorrhagic Brain Cavernous Malformations

K.D. Flemming, S. Kumar, G. Lanzino and W. Brinjikji
American Journal of Neuroradiology June 2019, 40 (6) 967-972; DOI: https://doi.org/10.3174/ajnr.A6076
K.D. Flemming
aFrom the Departments of Neurology (K.D.F., S.K.)
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S. Kumar
aFrom the Departments of Neurology (K.D.F., S.K.)
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G. Lanzino
bNeurosurgery (G.L.)
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W. Brinjikji
cNeuroradiology (W.B.), Mayo Clinic, Rochester, Minnesota.
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    Fig 1.

    Typical evolution of a hemorrhagic CM on MR imaging with time. Row 1, A hemorrhagic CM in the pons at the time of acute focal symptoms. MR imaging demonstrates subacute hemorrhage with increased T1 and T2 signal, with surrounding edema on FLAIR. In this patient, there was no enhancement of the lesion. DWI and ADC maps demonstrate low signal intensity. Rows 2 and 3, The evolution of the lesion 1 and 8 months later, respectively. The edema is reduced by 1 month and absent at 8 months. The lesion decreases in size, but there remains an increased T1 signal. DWI remains low signal intensity throughout. The ADC map demonstrates low or mixed intensity by 8 months.

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    Fig 2.

    Radiologic evolution of hemorrhagic cavernous malformations. Row 1, An acute hemorrhage into a medullary cavernous malformation with surrounding FLAIR hyperintensity. There is a small developmental venous anomaly on contrast imaging. A follow-up MR imaging (row 2) was performed 3 months later. The cavernous malformation has evolved from a Zabramski type I to type III lesion. There is no persistent edema, and the ADC and DWI demonstrate hypointensity.

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    Fig 3.

    Overview of the evolutionary MR imaging changes of hemorrhagic CM with time. This graphic display shows the percentage of patients with particular MR imaging characteristics at baseline and ≤90 days, 91–365 days, and >365 days.

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    Table 1:

    Demographics of patients with sporadic, brain CMs (n = 51)

    Clinical Information
    Sex31 (60.8%) male
    Age at diagnosis (yr)Median, 38.3 (range, 17.7–70.5)
    Race45 (90.0%) Caucasian
    Clinical presentation (No.) (%)Focal neurologic deficit, 37 (72.6%)
    Seizure, 4 (7.8%)
    Headache, 8 (15.6%)
    Spell, not seizure, 1 (2.0%)
    Other, 1 (2.0%)
    Initial MRI scan brain (No.)
        Symptom onset to first MRI (day)Median, 4 (range, 0–30)
        >1 CMa3 (5.88%)
        Size (mm)Median, 12.7 (range, 4.7–34.7)
        Brain stem location31 (60.8%)
        LocationCortical, 12 (23.5%)
    Supratentorial, subcortical, 6 (11.8%)
    Posterior fossa, 32 (62.7%)
    Intraventricular, 1 (2.0%)
        Zabramski lesion typeType I, 48 (94.2%)
    Type II, 3 (5.8%)
        DVA21/42b (50.0%)
        T1 hyperintensity48 (94.1%)
        Enhancement with Gd7/42b (16.7%)
        Edema39 (76.5%)
        DWI intensityLow, 26/49b (53.1%)
    Mixed, 21/49b (42.9%)
    High, 2/49b (4.0%)
        ADC map intensityLow, 19/42b (45.2%)
    Mixed, 23/42b (54.8%)
    High, 0
        Perilesional high T1 signal17/51 (33.3%)
    • ↵a These patients had multiple CMs bordering a DVA; thus, they were considered sporadic lesions.

    • ↵b Nine patients did not have gadolinium sequences, 3 did not have DWI, and 9 did not have ADC imaging.

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    Table 2:

    Evolution of MRI changes on follow-up imaging at specific time intervalsa

    ≤90 Days91–365 Days>365 Days
    No.282423
    Time to follow-up MRI (day)Median, 46 (range, 12–90)Median, 159.5 (range, 92–365)Median, 1136 (range, 382-3022)
    Follow-up MRI demonstrated rebleed (No.)536
    T1 hyperintensity17/23 (73.9%)12/21 (57.1%)8/16 (50%)
    T1 hyperintensity (moderate to significant)9/17 (52.9%)6/12 (50%)1/8 (12.5%)
    Enhancement with gadolinium6/22 (27.3%)7/20 (35%)9/16 (56.2%)
    Degree of enhancement (moderate to significant)2/6 (33.3%)1/7 (14.3%)2/9 (22.2%)
    Edema2/23 (8.7%)00
    Degree of edema (moderate to significant)1/2 (50%)––
    DWI low intensity13/23 (56.5%)12/17 (70.1%)13/16 (81.2%)
    ADC low intensity14/19 (73.7%)12/16 (75.0%)8/13 (61.5%)
    Change to Zabramski type II or III lesion15/23 (65.2%)17/21 (80.9%)16/16 (100%)
    Average size change (compared with original MRI) (mm)Median, 1.4 (range, −6.5 to +1.7)Median, 2.05 (range, −24.7 to +1.1)Median, −3.3 (range, −9.7 to +8.9)
    • Note:—– indicates no data.

    • ↵a Denominators noted are based on the availability of the particular MRI sequence.

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    Table 3:

    Evolution of MRI changes on follow-up brain imaging <1 year versus >1 yeara

    ≤365 Days>365 Days
    No.3723
    Median time to MRI (day)101 (range, 5–263)1136 (range, 382–3022)
    No. with recurrent hemorrhage86
    T1 hyperintensity19/32 (59.4%)8/16 (50.0%)
    T1 hyperintensity (moderate to significant)10/19 (56.2%)1/9 (11.1%)
    Enhancement with gadolinium8/31 (25.8%)9/16 (56.2%)
    Edema2/32 (6.2%)0
    DWI low intensity20/29 (68.9%)13/16 (81.2%)
    ADC low intensity19/28 (67.9%)8/13 (61.5%)
    Change to Zabramski type II or III lesions27/32 (84.4%)16/16 (100%)
    Average size change (mm) (range)Median, −1.4 (−24.7 to +1.1)Median, −3.3 (−9.7 to +8.9)
    • ↵a Denominators noted are based on the availability of the particular MRI sequence.

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American Journal of Neuroradiology: 40 (6)
American Journal of Neuroradiology
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1 Jun 2019
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Cite this article
K.D. Flemming, S. Kumar, G. Lanzino, W. Brinjikji
Baseline and Evolutionary Radiologic Features in Sporadic, Hemorrhagic Brain Cavernous Malformations
American Journal of Neuroradiology Jun 2019, 40 (6) 967-972; DOI: 10.3174/ajnr.A6076

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Baseline and Evolutionary Radiologic Features in Sporadic, Hemorrhagic Brain Cavernous Malformations
K.D. Flemming, S. Kumar, G. Lanzino, W. Brinjikji
American Journal of Neuroradiology Jun 2019, 40 (6) 967-972; DOI: 10.3174/ajnr.A6076
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