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Research ArticleBrain
Open Access

Neurovascular Manifestations in Hereditary Hemorrhagic Telangiectasia: Imaging Features and Genotype-Phenotype Correlations

T. Krings, H. Kim, S. Power, J. Nelson, M.E. Faughnan, W.L. Young, K.G. terBrugge and the Brain Vascular Malformation Consortium HHT Investigator Group
American Journal of Neuroradiology May 2015, 36 (5) 863-870; DOI: https://doi.org/10.3174/ajnr.A4210
T. Krings
aFrom the Division of Neuroradiology (T.K., S.P., K.G.t.B.), Department of Medical Imaging
bDivision of Neurosurgery (T.K.), Department of Surgery, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada
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H. Kim
cDepartment of Anesthesia and Perioperative Care (H.K., J.N., W.L.Y.), Center for Cerebrovascular Research
dDepartment of Epidemiology and Biostatistics (H.K.), University of California San Francisco, San Francisco, California
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S. Power
aFrom the Division of Neuroradiology (T.K., S.P., K.G.t.B.), Department of Medical Imaging
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J. Nelson
cDepartment of Anesthesia and Perioperative Care (H.K., J.N., W.L.Y.), Center for Cerebrovascular Research
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M.E. Faughnan
eDivision of Respirology (M.E.F.), Department of Medicine and Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada
fDivision of Respirology (M.E.F.), Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
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W.L. Young
cDepartment of Anesthesia and Perioperative Care (H.K., J.N., W.L.Y.), Center for Cerebrovascular Research
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K.G. terBrugge
aFrom the Division of Neuroradiology (T.K., S.P., K.G.t.B.), Department of Medical Imaging
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  • Fig 1.
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    Fig 1.

    Left ICA angiogram, lateral view, depicts typical features of a capillary vascular malformation in the left frontal opercular region, with a subcentimeter vascular blush identified in the arterial (A) persisting into early venous phase (B, arrow), without evidence of arteriovenous shunting. On MR imaging, this appears as a focal region of hyperintensity on axial T2 FLAIR imaging (C, arrow), with fluffy enhancement on coronal gadolinium-enhanced T1-weighted imaging (D, arrow). No dilated arterial feeder or dilated draining vein is seen.

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    Fig 2.

    Lateral projection of right ICA angiogram (A–C) and axial T1-weighted gadolinium-enhanced MR imaging (D) demonstrate the typical imaging features of a capillary vascular malformation in a 17-year-old male patient with HHT. A focal subcentimeter blush (arrows) is identified on the arterial phase of a right carotid angiogram, in the frontal, temporal, and parietal regions, in keeping with multiple capillary telangiectasia. Magnified view of the right parietal lesion shows typical angiographic features, with vascular blush identified in the arterial (B) persisting into early venous phase (C); no arteriovenous shunting, dilated arterial feeder, or dilated draining vein are seen. MR imaging appearance of the right parietal lesion demonstrates the typical features of fluffy contrast enhancement in a superficial cortical/subcortical location, without abnormal vascular dilation (D, arrow).

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    Fig 3.

    Lateral view of a right ICA angiogram in a 43-year-old male patient with HHT demonstrates a capillary vascular malformation in the right anterior parietal region. A subcentimeter blush is seen in the arterial phase (A, arrow), which persists in the late arterial phase (B) without evidence of arteriovenous shunting.

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    Fig 4.

    Left ICA catheter angiogram (A and B), microcatheter injection (C and D), axial T2-weighted (E), and contrast-enhanced T1-weighted MR imaging (F) demonstrate imaging findings of a typical arteriovenous malformation. Anteroposterior projection of a left ICA injection demonstrates filling of the AVM nidus through an enlarged anterior temporal branch of the left MCA in the early arterial phase (A, arrow). There is arteriovenous shunting with early venous drainage through an enlarged left inferior temporal vein (B, arrows). Microcatheter injection in frontal (C) and lateral (D) projections demonstrates a typical glomerular well-defined compact nidus supplied by a single terminal arterial feeder with shunting into a dilated vein. MR imaging shows the superficial location of the AVM, with vascular flow voids seen on T2-weighted imaging (E, arrow) and enhancement on postgadolinium T1-weighted imaging (F, arrow). Evidence of previous hemorrhage related to AVM rupture, with a slit-like hematoma cavity in the left inferior frontal lobe, and surrounding hemosiderin staining (E, black arrow).

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    Fig 5.

    Typical MR imaging features of an arteriovenous malformation in a 50-year-old male patient with HHT. Axial T2-weighted imaging demonstrates a cluster of flow voids in the left occipital lobe, in keeping with a vascular nidus (A). A linear flow void of the dilated draining vein is seen inferior to the nidus on axial T2 (B) and coronal postcontrast T1-weighted imaging (C). Axial MRA MIP demonstrates a compact glomerular-type nidus in the left occipital lobe (D).

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    Fig 6.

    Right ICA catheter angiogram in lateral (A) and frontal (B) projections demonstrates 2 separate high-flow single-hole pial arteriovenous fistulas, 1 in the right frontal lobe and 1 in the right temporal lobe. Arterial supply to each fistula is through a single enlarged right MCA branch, which empties directly into a large venous pouch. Venous drainage is superficial, with both fistulas draining through enlarged cortical veins to the superior sagittal sinus. On axial T2-weighted MR imaging (C and D) venous pouches appear as flow voids and exert mass effect on the adjacent right temporal lobe. Evidence of venous congestion with venous reflux through dilated transdmedullary veins to the deep venous system is demonstrated on a coronal reconstruction of CTA (arrows).

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    Fig 7.

    Lateral view of a left ICA angiogram in an 8-year-old male patient with HHT. Angiography in early arterial (A) and venous (B) phases demonstrates a high-flow single-hole pial arteriovenous fistula in the left frontal lobe. Arterial supply is through a single enlarged prefrontal branch of the left MCA, which empties directly into a large venous pouch. Venous drainage is superficial through an enlarged cortical vein to the superior sagittal sinus.

Tables

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    Table 1:

    Overview of 75 subjects with HHT and brain vascular malformations

    CharacteristicSummarya
    Demographics
        Female sex41/75 (55%)
        Age at enrollment (yr) (n = 75)36.6 ± 19.9
        Age at brain malformation diagnosis (yr) (n = 68)30.1 ± 19.7
    HHT-related symptoms
        Epistaxis66/73 (90%)
        Anemia20/72 (28%)
        GI bleeding5/67 (7%)
        Pulmonary AVM45/69 (65%)
        Liver VM4/66 (6%)
    HHT-causing mutation
        ALK113/45 (29%)
        Endoglin27/45 (60%)
        SMAD41/45 (2%)
        All test findings negative4/45 (9%)
    • Note:—GI indicates gastrointestinal; VM, vascular malformations.

    • ↵a Summary is the No. of observations with specified value over the total No. (and the percentage) or the mean ± SD.

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    Table 2:

    Brain vascular malformation phenotypes of 75 subjects with HHT

    Capillary Vascular Malformation
    012+
    0 AVMs/AVFs1 (1%)a17 (23%)18 (24%)b
    1 AVM20 (27%)5 (7%)3 (4%)
    2 AVMs1 (1%)0 (0%)1 (1%)
    1 AVF4 (5%)1 (1%)0 (0%)
    2 AVFs1 (1%)1 (1%)0 (0%)
    1 AVM and 1 AVF2 (3%)0 (0%)0 (0%)
    • ↵a This individual had 1 dural arteriovenous fistula only.

    • ↵b One individual in this group had a developmental venous anomaly.

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    Table 3:

    Characteristics of 80 capillary vascular malformations

    CharacteristicSummarya
    Size of maximal dimension (mm) (n = 80)4.8 ± 2.1
    Lobe
        Frontal30/80 (38%)
        Parietal16/80 (20%)
        Occipital14/80 (18%)
        Temporal10/80 (13%)
        Cerebellum7/80 (9%)
        Brain stem2/80 (3%)
        Thalamus/basal ganglia1/80 (1%)
    Location
        Deep3/80 (4%)
        Subcortical14/80 (18%)
        Superficial63/80 (79%)
    MRI visible66/71 (93%)
    • ↵a Summary is the No. of observations with specified value over the total No. (and the percentage) or the mean ± SD.

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    Table 4:

    Characteristics of 34 AVMs

    CharacteristicSummarya
    Size of maximal dimension (mm) (n = 34)18.3 ± 5.3
    Eloquent13/34 (38%)
    Deep venous drainage5/31 (16%)
    Spetzler-Martin score
        116/31 (52%)
        212/31 (39%)
        32/31 (6%)
        41/31 (3%)
        50/31 (0%)
    Lobe
        Frontal14/34 (41%)
        Parietal5/34 (15%)
        Occipital4/34 (12%)
        Temporal5/34 (15%)
        Cerebellum2/34 (6%)
        Brain stem2/34 (6%)
        Thalamus/basal ganglia2/34 (6%)
    Location
        Deep4/34 (12%)
        Subcortical5/34 (15%)
        Superficial25/34 (74%)
    Nidus en passage (vs terminal)2/20 (10%)
    Diffuse nidus (vs sharp)6/34 (18%)
    Pial-to-pial collateralization5/31 (16%)
    Moyamoya-type changes0/33 (0%)
    Stenoses on arteries0/31 (0%)
    Type, pial (vs choroidal)33/34 (97%)
    Associated aneurysms0/30 (0%)
    Multiple draining veins3/29 (10%)
    Venous ectasia8/31 (26%)
    Venous reflux1/29 (3%)
    Pseudophlebitic pattern0/29 (0%)
    • ↵a Summary is the No. of observations with specified value over the total No. (and the percentage) or the mean ± SD.

    • View popup
    Table 5:

    Characteristics of 11 AVFs

    CharacteristicSummarya
    Single hole with pouch10/11 (91%)
    Lobe
        Frontal4/11 (36%)
        Parietal0/11 (0%)
        Occipital3/11 (27%)
        Temporal3/11 (27%)
        Cerebellum0/11 (0%)
        Brain stem0/11 (0%)
        Thalamus/basal ganglia1/11 (9%)
    Location
        Deep1/11 (9%)
        Subcortical0/11 (0%)
        Superficial10/11 (91%)
    Pial-to-pial collateralization3/11 (27%)
    Moyamoya-type changes1/11 (9%)
    Stenoses on arteries1/11 (9%)
    Type, pial (vs choroidal)2/11 (18%)
    Associated aneurysms2/11 (18%)
    Multiple draining veins5/11 (45%)
    Venous ectasia11/11 (100%)
    Venous reflux0/11 (0%)
    Pseudophlebitic pattern3/11 (27%)
    • ↵a Summary is the No. of observations with specified value over the total No. (and the percentage).

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American Journal of Neuroradiology: 36 (5)
American Journal of Neuroradiology
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T. Krings, H. Kim, S. Power, J. Nelson, M.E. Faughnan, W.L. Young, K.G. terBrugge, the Brain Vascular Malformation Consortium HHT Investigator Group
Neurovascular Manifestations in Hereditary Hemorrhagic Telangiectasia: Imaging Features and Genotype-Phenotype Correlations
American Journal of Neuroradiology May 2015, 36 (5) 863-870; DOI: 10.3174/ajnr.A4210

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Neurovascular Manifestations in Hereditary Hemorrhagic Telangiectasia: Imaging Features and Genotype-Phenotype Correlations
T. Krings, H. Kim, S. Power, J. Nelson, M.E. Faughnan, W.L. Young, K.G. terBrugge, the Brain Vascular Malformation Consortium HHT Investigator Group
American Journal of Neuroradiology May 2015, 36 (5) 863-870; DOI: 10.3174/ajnr.A4210
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