Investig Magn Reson Imaging.  2015 Sep;19(3):146-152. 10.13104/imri.2015.19.3.146.

Associated Brain Parenchymal Abnormalities in Developmental Venous Anomalies: Evaluation with Susceptibility-weighted MR Imaging

Affiliations
  • 1Department of Radiology and Gyeongsang National University School of Medicine, Jinju, Korea. choids@gnu.ac.kr
  • 2Gyeongsang Institute of Health Science, Gyeongsang National University School of Medicine, Jinju, Korea.

Abstract

PURPOSE
The purpose of this study was to evaluate the associated brain parenchymal abnormalities of developmental venous anomalies (DVA) with susceptibility-weighted image (SWI).
MATERIALS AND METHODS
Between January 2012 and June 2013, 2356 patients underwent brain MR examinations with contrast enhancement. We retrospectively reviewed their MR examinations and data were collected as per the following criteria: incidence, locations, and associated parenchymal signal abnormalities of DVAs on T2-weighted image, fluid-attenuated inversion recovery (FLAIR), and SWI. Contrast enhanced T1-weighted image was used to diagnose DVA.
RESULTS
Of the 2356 patients examined, 57 DVAs were detected in 57 patients (2.4%); 47 (82.4%) were in either lobe of the supratentorial brain, 9 (15.7%) were in the cerebellum, and 1 (1.7%) was in the pons. Of the 57 DVAs identified, 20 (35.1%) had associated parenchymal abnormalities in the drainage area. Among the 20 DVAs which had associated parenchymal abnormalities, 13 showed hemorrhagic foci on SWI, and 7 demonstrated only increased parenchymal signal abnormalities on T2-weighted and FLAIR images. In 5 of the 13 patients (38.5%) who had hemorrhagic foci, the hemorrhagic lesions were demonstrated only on SWI.
CONCLUSION
The overall incidence of DVAs was 2.4%. Parenchymal abnormalities were associated with DVAs in 35.1% of the cases. On SWI, hemorrhage was detected in 22.8% of DVAs. Thus, we conclude that SWI might give a potential for understanding of the pathophysiology of parenchymal abnormalities in DVAs.

Keyword

Cerebral developmental venous anomaly; Hemorrhage; MR; Susceptibility-weighted imaging (SWI)

MeSH Terms

Brain*
Cerebellum
Drainage
Hemorrhage
Humans
Incidence
Magnetic Resonance Imaging*
Pons
Retrospective Studies

Figure

  • Fig. 1 A 55-year-old female with a DVA. Enhanced T1-weighted image (a) and SWI (b) show a DVA in the left parietal lobe (short arrows). T2-weighted (c) and FLAIR (d) images reveal parenchymal signal abnormalities in and around the DVA (long arrows).

  • Fig. 2 A 36-year-old female with a DVA. Enhanced T1-weighted (a), SWI (b), T2-weighted (c) and FLAIR (d) images show a DVA (long arrows) and an associated hemorrhagic lesion (short arrows) in the right frontal lobe and corpus callosum. Both the DVA and hemorrhagic lesion are more conspicuously demonstrated on SWI than on T2-weighted and FLAIR images.

  • Fig. 3 A 59-year-old female with a DVA. Enhanced T1-weighted image (a) and SWI (b) show a DVA in the right frontoparietal lobe (long arrows). There is also a focal hemorrhagic lesion on SWI (short arrows). T2-weighted (c) and FLAIR (d) images demonstrate hyperintense signal abnormalities in the drainage territory of the DVA (long arrows). The hemorrhagic lesion is seen as a focal cystic lesion (short arrows).


Reference

1. Ruiz DS, Yilmaz H, Gailloud P. Cerebral developmental venous anomalies: current concepts. Ann Neurol. 2009; 66:271–283.
2. San Millan Ruiz D, Gailloud P. Cerebral developmental venous anomalies. Childs Nerv Syst. 2010; 26:1395–1406.
3. Sarwar M, McCormick WF. Intracerebral venous angioma. Case report and review. Arch Neurol. 1978; 35:323–325.
4. Garner TB, Del Curling O Jr, Kelly DL Jr, Laster DW. The natural history of intracranial venous angiomas. J Neurosurg. 1991; 75:715–722.
5. Santucci GM, Leach JL, Ying J, Leach SD, Tomsick TA. Brain parenchymal signal abnormalities associated with developmental venous anomalies: detailed MR imaging assessment. AJNR Am J Neuroradiol. 2008; 29:1317–1323.
6. San Millan Ruiz D, Delavelle J, Yilmaz H, et al. Parenchymal abnormalities associated with developmental venous anomalies. Neuroradiology. 2007; 49:987–995.
7. Wilms G, Bleus E, Demaerel P, et al. Simultaneous occurrence of developmental venous anomalies and cavernous angiomas. AJNR Am J Neuroradiol. 1994; 15:1247–1254. discussion 1255-1257
8. Huber G, Henkes H, Hermes M, Felber S, Terstegge K, Piepgras U. Regional association of developmental venous anomalies with angiographically occult vascular malformations. Eur Radiol. 1996; 6:30–37.
9. Abe T, Singer RJ, Marks MP, Norbash AM, Crowley RS, Steinberg GK. Coexistence of occult vascular malformations and developmental venous anomalies in the central nervous system: MR evaluation. AJNR Am J Neuroradiol. 1998; 19:51–57.
10. Uchino A, Hasuo K, Matsumoto S, et al. Cerebral venous angiomas associated with hemorrhagic lesions. Their MRI manifestations. Clin Imaging. 1996; 20:157–163.
11. Sehgal V, Delproposto Z, Haacke EM, et al. Clinical applications of neuroimaging with susceptibility-weighted imaging. J Magn Reson Imaging. 2005; 22:439–450.
12. Tong KA, Ashwal S, Obenaus A, Nickerson JP, Kido D, Haacke EM. Susceptibility-weighted MR imaging: a review of clinical applications in children. AJNR Am J Neuroradiol. 2008; 29:9–17.
13. Tsui YK, Tsai FY, Hasso AN, Greensite F, Nguyen BV. Susceptibility-weighted imaging for differential diagnosis of cerebral vascular pathology: a pictorial review. J Neurol Sci. 2009; 287:7–16.
14. Haacke EM, Mittal S, Wu Z, Neelavalli J, Cheng YC. Susceptibility-weighted imaging: technical aspects and clinical applications, part 1. AJNR Am J Neuroradiol. 2009; 30:19–30.
15. de Souza JM, Domingues RC, Cruz LC Jr, Domingues FS, Iasbeck T, Gasparetto EL. Susceptibility-weighted imaging for the evaluation of patients with familial cerebral cavernous malformations: a comparison with t2-weighted fast spin-echo and gradient-echo sequences. AJNR Am J Neuroradiol. 2008; 29:154–158.
16. Takasugi M, Fujii S, Shinohara Y, Kaminou T, Watanabe T, Ogawa T. Parenchymal hypointense foci associated with developmental venous anomalies: evaluation by phase-sensitive MR Imaging at 3T. AJNR Am J Neuroradiol. 2013; 34:1940–1944.
17. Jung HN, Kim ST, Cha J, et al. Diffusion and perfusion MRI findings of the signal-intensity abnormalities of brain associated with developmental venous anomaly. AJNR Am J Neuroradiol. 2014; 35:1539–1542.
18. Saito Y, Kobayashi N. Cerebral venous angiomas: clinical evaluation and possible etiology. Radiology. 1981; 139:87–94.
19. Senegor M, Dohrmann GJ, Wollmann RL. Venous angiomas of the posterior fossa should be considered as anomalous venous drainage. Surg Neurol. 1983; 19:26–32.
20. Thomas B, Somasundaram S, Thamburaj K, et al. Clinical applications of susceptibility weighted MR imaging of the brain - a pictorial review. Neuroradiology. 2008; 50:105–116.
21. Haacke EM, Xu Y, Cheng YC, Reichenbach JR. Susceptibility weighted imaging (SWI). Magn Reson Med. 2004; 52:612–618.
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