Hemodynamic Effects of Developmental Venous Anomalies with and without Cavernous Malformations

被引:43
|
作者
Sharma, A. [1 ,4 ,5 ]
Zipfel, G. J. [1 ,2 ,3 ,4 ,5 ]
Hildebolt, C. [1 ]
Derdeyn, C. P. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Neurol Surg, St Louis, MO 63110 USA
[4] Barnes Jewish Hosp South, Dept Radiol, St Louis, MO USA
[5] St Louis Childrens Hosp, Dept Radiol, St Louis, MO 63178 USA
关键词
STURGE-WEBER-SYNDROME; PERFUSION; BRAIN; ANGIOMAS; HISTORY; VOLUME;
D O I
10.3174/ajnr.A3516
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Perfusion imaging was done in patients with developmental venous anomalies with and without accompanying cavernous malformations. The normal-appearing brain surrounding DVAs showed higher blood volume, longer mean transit time, and variable changes in blood flow. DVAs with cavernomas showed greater MTT prolongation and less blood flow indicating greater restrictive effects upon the adjacent brain. The authors offer some ingenious and interesting explanations for these findings. BACKGROUND AND PURPOSE: Association between developmental venous anomalies is well known, but remains unexplained. Our aim was to study possible hemodynamic differences around developmental venous anomalies with and without cavernous malformations. MATERIALS AND METHODS: In this prospective study approved by the institutional review board, PWI was performed in 24 patients with 25 DVAs (10 with and 15 without CMs) who consented to participate. We calculated relative cerebral blood volume, relative cerebral blood flow, and relative mean transit time for the brain surrounding the DVA tributaries in reference to contralateral mirror image locations. Corresponding control values (cCBV, cCBF, and cMTT) were generated in a similar fashion for remote ipsilateral regions with normal venous drainage, also in reference to contralateral mirror image locations. Perfusion parameters for DVAs and control regions were tested for differences between groups with the t test for independent or paired samples (or the nonparametric equivalents). Similar testing was done for perfusion parameters for DVAs with and without CMs. RESULTS: Normal-appearing brain surrounding DVAs showed increased rCBV (median = 2.98; range = 1.39-6.61), increased rCBF (median = 2.00, range = 0.79-4.43), and increased rMTT (mean = 1.46; 95% confidence interval, 1.32-1.59). These were significantly higher than median cCBV (0.99; 95% confidence interval, 0.89-1.06; P < .01), median cCBF (1.00; 95% confidence interval, 0.94-1.27; P < .01), and mean cMTT (1.00; 95% confidence interval, 0.98-1.02; P < .01), respectively. Mean rMTT (1.70; 95% confidence interval, 1.46-1.93) for DVAs with CMs was higher than mean rMTT (1.29; 95% confidence interval, 1.19-1.40; P < .01) for DVAs without CMs. CONCLUSIONS: DVAs are strongly associated with altered hemodynamics. Significant differences in these hemodynamic alterations for DVAs with and without CMs suggest their possible role in the formation of CMs.
引用
收藏
页码:1746 / 1751
页数:6
相关论文
共 50 条
  • [31] Developmental venous anomalies of the brain in children — imaging spectrum and update
    Luke L. Linscott
    James L. Leach
    Blaise V. Jones
    Todd A. Abruzzo
    Pediatric Radiology, 2016, 46 : 394 - 406
  • [32] Developmental venous anomalies with capillary stain: a subgroup of symptomatic DVAs?
    Roccatagliata, Luca
    van den Berg, Rene
    Soderman, Michael
    Boulin, Anne
    Condette-Auliac, Stephanie
    Rodesch, Georges
    NEURORADIOLOGY, 2012, 54 (05) : 475 - 480
  • [33] Epilepsy and cerebral developmental venous anomalies (DVAs): A systematic review
    El Meskine, Tahir
    Li, Jimmy
    Reise, Julia
    Toffa, Denahin Hinnoutondji
    EPILEPTIC DISORDERS, 2023, 25 (02) : 209 - 217
  • [34] Risks and Benefits of Surgical Excision of Orbital Cavernous Venous Malformations (So-Called Cavernous Hemangioma): Factors Influencing the Outcome
    Strianese, Diego
    Bonavolonta, Giulio
    Iuliano, Adriana
    Mariniello, Giuseppe
    Elefante, Andrea
    Liuzzi, Raffaele
    OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY, 2021, 37 (03) : 248 - 254
  • [35] Evaluation of sporadic intracranial cavernous malformations for detecting associated developmental venous anomalies: added diagnostic value of C-arm contrast-enhanced cone-beam CT to routine contrast-enhanced MRI
    Kocak, Burak
    Kizilkilic, Osman
    Zeynalova, Amalya
    Korkmazer, Bora
    Kocer, Naci
    Islak, Civan
    EUROPEAN RADIOLOGY, 2019, 29 (02) : 783 - 791
  • [36] Infratentorial Developmental Venous Abnormalities and Inflammation Increase Odds of Sporadic Cavernous Malformation
    Kumar, Shivram
    Lanzino, Giuseppe
    Brinjikji, Waleed
    Hocquard, Kate W.
    Flemming, Kelly D.
    JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2019, 28 (06) : 1662 - 1667
  • [37] The Central Vein: FLAIR Signal Abnormalities Associated with Developmental Venous Anomalies in Patients with Multiple Sclerosis
    Rogers, D. M.
    Shah, L. M.
    Wiggins, R. H.
    AMERICAN JOURNAL OF NEURORADIOLOGY, 2018, 39 (11) : 2007 - 2013
  • [38] Cavernous venous malformations in and around the central nervous system. Part 1: Dural and extradural
    Ibn Essayed, Walid
    Bernstock, Joshua D.
    Chen, Jason A.
    Kappel, Ari D.
    Ng, Patrick R.
    Du, Rose
    JOURNAL OF NEUROSURGERY, 2024, 140 (02) : 735 - 745
  • [39] Somatic GJA4 gain-of-function mutation in orbital cavernous venous malformations
    Hongo, Hiroki
    Miyawaki, Satoru
    Teranishi, Yu
    Mitsui, Jun
    Katoh, Hiroto
    Komura, Daisuke
    Tsubota, Kinya
    Matsukawa, Takashi
    Watanabe, Masakatsu
    Kurita, Masakazu
    Yoshimura, Jun
    Dofuku, Shogo
    Ohara, Kenta
    Ishigami, Daiichiro
    Okano, Atsushi
    Kato, Motoi
    Hakuno, Fumihiko
    Takahashi, Ayaka
    Kunita, Akiko
    Ishiura, Hiroyuki
    Shin, Masahiro
    Nakatomi, Hirofumi
    Nagao, Toshitaka
    Goto, Hiroshi
    Takahashi, Shin-Ichiro
    Ushiku, Tetsuo
    Ishikawa, Shumpei
    Okazaki, Mutsumi
    Morishita, Shinichi
    Tsuji, Shoji
    Saito, Nobuhito
    ANGIOGENESIS, 2023, 26 (01) : 37 - 52
  • [40] Neonatal Developmental Venous Anomalies: Clinicoradiologic Characterization and Follow-Up
    Geraldo, A. F.
    Messina, S. S.
    Tortora, D.
    Parodi, A.
    Malova, M.
    Morana, G.
    Gandolfo, C.
    D'Amico, A.
    Herkert, E.
    Govaert, P.
    Ramenghi, L. A.
    Rossi, A.
    Severino, M.
    AMERICAN JOURNAL OF NEURORADIOLOGY, 2020, 41 (12) : 2370 - 2376