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Goyal, Singh, Bansal, and Paliwal: Anatomical Variations of Cerebral MR Venography: Is Gender Matter?

Abstract

Purpose

Knowledge of variations in the cerebral dural venous sinus anatomy seen on magnetic resonance (MR) venography is essential to avoid over-diagnosis of cerebral venous sinus thrombosis (CVST). Very limited data is available on gender difference of the cerebral dural venous sinus anatomy variations.

Materials and Methods

A retrospective study was conducted to study the normal anatomy of the intracranial venous system and its normal variation, as depicted by 3D MR venography, in normal adults and any gender-related differences.

Results

A total of 1654 patients (582 men, 1072 women, age range 19 to 86 years, mean age: 37.98±13.83 years) were included in the study. Most common indication for MR venography was headache (75.4%). Hypoplastic left transverse sinus was the most common anatomical variation in 352 (21.3%) patients. Left transverse sinus was hypoplastic in more commonly in male in comparison to female (24.9% versus 19.3%, p = 0.009). Most common variation of superior sagittal sinus (SSS) was atresia of anterior one third SSS (15, 0.9%). Except hypoplastic left transverse sinus, rest of anatomical variations of the transverse and other sinuses were not significantly differ among both genders.

Conclusion

Hypoplastic left transverse sinus is the most common anatomical variation and more common in male compared to female in the present study. Other anatomical variations of dural venous sinuses are not significantly differ among both genders.

Magnetic resonance venography (MRV) plays important role in studying anatomy of the intracranial venous system and its variation to look for any pathology and misinterpretation of its normal variation [12]. Visualization of intracranial venous system is important in certain clinical situations such as diagnosis of cortical venous thrombosis and assessment of the patency of the venous sinus lumina encased by meningioma.
It can also be done from various other methods like CT Venogram & Conventional catheter venography but MR Venography is having overdue benefits like it is non-invasive, does not require ionic radiation exposure or use of any paramagnetic contrast agent administration because of Time of flight (TOF) and Phase Contrast (PC) MR technique, which is most commonly use and provides higher signal to noise and short image time [34].
MRV can even evaluate pathology in the vessels which are close to the bony surface which are hard to visualize on CT Angiography due to the artifacts [5]. There are also few disadvantages like it required longer acquisition time but it can be overcome by newly developed parallel imaging technique, due to narrow bore size and loud noise some patients experience claustrophobia which can be overcome by ear plugs and open or wide bore machines, due to the movement it causes artifacts & signal loss. A number of studies are available on variation of magnetic resonance venography but no literature is available on gender difference of MRV variations in best of our knowledge [367891011].
The purpose of our study is to retrospectively study the normal anatomy of the intracranial venous system and its normal variation, as depicted by 3D MRV, in normal adults and any gender-related differences.

MATERIALS AND METHODS

Patients, those were sent for MRV examination in tertiary care teaching hospital from January 2011 to December 2013 were enrolled in this study. MRV data of 2000 patients during study period was retrospectively reviewed. Patients with more than 18 years of age were included in this study. Patients with any congenital or acquired intracranial abnormality, venous thrombosis or previous surgery were excluded from the study. As this study is the retrospective, institutional review board clearance was not sought.
210 patients were excluded because of structural pathology (congenital or acquired) and presence of cortical venous thrombosis. One hundred thirty six patients were 18 or less than 18 years old, therefore excluded. MRV data of 1654 patients were included in final analysis. Clinical indication for MRI and MRV was noted in each patient.

MR Imaging

MR imaging was performed with superconducting 1.5-T MR machine (Achiva version 1.3; Philips, best the Netherland) and standard head coil. Three-dimensional MR venography was performed in the coronal plane by using the following parameters: TE-50, TR-500 FOV-230-250, Slice thickness 1 mm, Matrix- 240 × 256, flip angle 50. Additional routine T2WI coronal and axial FLAIR sequences were also performed.
The slice thickness of 1.2 mm was acquired with contiguous sections using matrix size of 256 × 256 and a nominal field of view (FOV) of 27 cm with TR (Time to Repeat) -22 milliseconds, TE (Time to Echo) - 7.4 milliseconds and flip angle of 15o. TRITE- 50/8.4. The velocity encoding applied was 30-40 cm per second. The images were displayed as 20 maximum intensity projection (MIP) images reconstructed from the source images at 9 degree increments.

Image analysis

Maximum intensity projections (MIPs) were created at the MR operating console for 3D-MR venography data set. The MIP images were viewed in the sagittal, transverse and coronal planes.
Source images from 3D MRV and MIP images were evaluated for anatomical variations of dural venous sinuses and presence of accessary sinuses. The dural venous sinuses included in this study are superior sagittal sinus, sigmoid sinus, transverse sinus, straight sinus and occipital sinus. The normal variations of transverse and sigmoid sinuses were noted (symmetry, hypoplasia and aplasia or atresia). The transverse sinuses were measured 1 cm from the Torcula heterophili and the sigmoid sinuses were measured 1 cm from the transverse sigmoid junctions. Their liner measurement were compared with the superior sagittal sinus. If the linear measurement was less than half the size of the superior sagittal sinus, it was considered hypoplastic and if not visualised it was considered aplastic or atrectic sinus. The internal jugular veins were not included in the study. The presence of arachnoid granulations were recorded. AGs are defined as well-defined CSF-like signal intensity protuberances extending into the dural sinus commonly associated with adjacent entering cortical veins.

Statistical Analysis

Numeric values were shown as the mean ± standard deviation (SD). Chi-square contingency analysis was used to explore the statistically significant difference of MRV variations among both males and females. A difference was considered significant at a P value of less than 0.05.

RESULTS

Our study included a total of 1654 patients (582 men, 1072 women, age range 19 to 86 years, mean age: 37.98±13.83 years). Mean age for men was 39.44±14.46 (range 19 to 86 years) and for women 37.19±13.41 (range 19 to 85 years).

Indications

Most common indication for MRV was headache (75.4%). Other indications were headache and vertigo (13.1%), Seizure (5.3%), Headache and vomiting (3.2%), vertigo (2%), altered sensorium (0.5%), forgetfulness (0.3%) and others (0.2%). Indications for MRV in both sexes have been summarized separately in Table 1.

Transverse and sigmoid sinus

Of the 1654 MR venograms obtained, the transverse sinus was found to be symmetrical in 1106 (66.9%) patients. Left transverse sinus was hypoplastic in 352 (21.3%) and aplastic/atrectic in 67 (4.1%) cases. Right transverse sinus was hypoplastic in 91 (5.5%) and aplastic/atrectic in 12 (0.7%) patients. 1.6% cases had bilateral hypoplastic transverse sinuses. In comparison, female had significantly more symmetrical transverse sinus than male (69.2% versus 62.5%, p value, 0.007). Left transverse sinus was hypoplastic in more commonly in male in comparison to female (24.9% versus 19.3%). This difference is statistically significant (p value, 0.009). Rest of normal variations of transverse sinus are not different in both the genders significantly.
1418 (85.7%) cases had symmetrical sigmoid sinuses. Left sigmoid sinus was hypoplastic or aplastic/atrectic in 11.4% (189) cases. Right sigmoid sinus was hypoplastic in 40 (2.4%) and aplastic/atrectic in 4 (0.2%). Three patients had hypoplastic bilateral sigmoid sinuses. Similar to transverse sinus, sigmoid sinus was symmetrical more commonly in female than male (87.2% versus 83%, p = 0.02). Difference between male and female for other variations of sigmoid sinus is not statistically signif icant. Anatomical variations and gender difference transverse and sigmoid sinuses have been summarized in Table 2.

Superior sagittal sinus

1616 (97.7%) patients had normal superior sagittal sinus. Most common variation of SSS was atresia of anterior one third SSS (15, 0.9%). Other variations were hypoplasia of middle part of SSS (13, 0.7%), hypoplasia of anterior one third of SSS (6, 0.4%), hypoplasia of anterior 2/3rd of SSS (3, 0.2%) and hypoplasia of anterior half of SSS (1, 0.1%). There was no statistically significant difference among males and females for these variations.
Flow gap in SSS was noted in 5 patients. Three cases had flow gap in posterior 1/3rd of SSS and 2 had in middle part of SSS. Anatomical variations and gender difference of superior sagittal sinus have been summarized in Table 3.

Accessory findings

Straight sinus (SS) was hypoplastic in 4 (0.2%) patients (1 (0.2%) male and 3 (0.3%) female). Difference among both genders is not statistically significant (p =0.92). No duplication or triplication of SS is noted in study population. The occipital sinus was identified in 23 (1.4%) patients. Oblique occipital sinus was noted in 13 (0.8%) patients. Five (0.9%) men and 18 (1.7%) women had occipital sinus. Gender difference for occipital sinus is not statistically significant (p value = 0.25). Arachnoid granulations were noted in 47 (2.8%) patients. Most common site for AGs was the lateral aspect of left TS (22, 1.3%). Other sites were the lateral aspect of right TS (10, 0.6%), middle part of SSS (9, 0.5%), posterior 1/3 of SSS (3, 0.2%), lateral aspect of bilateral TS (2, 0.1%) and left sigmoid sinus (1, 0.7%). Normal anatomical variations of cerebral dural venous sinuses on MRV have been illustrated in Figure 1.

DISCUSSION

The study was conducted to evaluate the normal anatomical variations in intracranial venous sinuses and gender differences of normal variations in the western Indian population. Most common indication to get MRV of brain was headache in this study. Hypoplastic left transverse sinus was the most common anatomical variation, predominantly in male compared to female. Other anatomical variations of the transverse and sigmoid sinuses were not significantly differ among both genders. Atresia of anterior one third of SSS was the most common variation of SSS, though not different among males and females.
Transverse sinus abnormalities were described by Alper et al [6]. Symmetrical transverse sinuses were reported in 31%. Left transverse sinus was hypoplastic in 39% and aplastic in 20% of cases. Right transverse sinus was hypoplastic in 6% and aplastic in 4%. In other study of 100 patients, 10% had symmetrical transverse sinuses, 35% hypoplastic left transverse sinus, 13% hypoplastic right transverse sinus and 1% had aplastic left transverse sinus [10]. In contrast, our study showed symmetrical transverse sinus in 66.9%, hypoplastic left transverse sinus in 21.3% and hypoplastic right transverse sinus in 5.5%. This difference in our study can be attributed to ethnical difference of the population.
The most frequent SSS variation is the hypoplasia of rostral third of the SSS second only to preferential drainage of SSS to one of the transverse sinus [1213]. Kaplan and Browder reported hypoplastic rostral SSS in 7 of 382 (1.8%) anatomic specimens in 1 series and in 12 of 201 (6%) specimens in a second anatomic series [14]. In the presence of complete hypoplastic rostral SSS, a pair of large parasagittal superior frontal cortical veins that run dorsally to join the origin of the SSS close to the coronal suture replace the absent rostral portion of the SSS [1213]. In a series of 100 patients, hypoplasia of rostral portion of SSS was studied by CT angiography. Complete hypoplastic rostral SSS was reported in 3% of patients [15]. In other study, this abnormality was reported in 9 % of cases [10]. In our study, atresia of SSS was noted in 0.9% and hypoplasia in 0.4%. Variation in incidence of hypoplastic or atrectic rostral third of SSS in different studies can be explained by use of different techniques or variation in inclusion criteria. Flow gaps in SSS and partial split SSS were reported in 24% and 12% in a study [10]. In other study, short segment flow gaps in SSS were observed in 5% of cases [11]. In our study, flow gaps were noted in 5 patients.
The occipital sinus, the smallest of the dural venous sinuses, which may be solitary, duplicated, or composed of a mesh of venous collaterals, is contained within the attached margin of the falx cerebelli and connects the torcula with the IJV [16]. Occipital sinuses were reported from 4 to 35.5% of cases in different studies [231117]. In a study of 100 children, persistent occipital sinuses were seen in 13% of patients less than 25 months of age but in only 2% of children older than 5 years [9]. This study support the hypothesis of involution of occipital sinus once most of the venous flow passes through the large dural sinuses as the child achieves an upright position. In our study, occipital sinus was identified in 1.4% of the patients. Over reported incidence of the occipital sinus in the literature may be attributed to wrong interpretation of other venous structures as occipital sinus or ethnical differences of studied populations. Accurate information of the incidence of occipital sinuses can be accumulated by future autopsy series.

Gender difference

The prevalence and symptomatology of many neurological and psychiatric conditions differ substantially between males and females. In a meta-analysis regarding sex differences in human brain morphology, differences in overall brain volumes are found to be sustained between males and females from newborns to individuals over 80 years old [18]. On average, males have larger intracranial volume (ICV) (12%), total brain volume (TBV) (11%), cerebrum (Cb) (10%), grey matter (GM) (9%), white matter (WM) (13%), cerebrospinal fluid (CSF) (11.5%) and cerebellum (Cbl) (9%) absolute volumes than females [18]. Difference between different brain structures among both genders can explain predisposition of some neuropsychiatric disorders to specific gender. Limited data is available on difference of intracranial vasculature among both the genders. In a small study of MR angiography of 30 cases, males were found to have larger diameter of posterior circulation arteries (posterior cerebral artery and basilar artery) compared to females [19]. Though there was no significant difference in anterior circulation arteries among males and females. Anatomic variations of sigmoid sinuses on phase contrast MR angiography were studied in a study of 257 cases of different age groups (5-82 years) [20]. Among 257 cases, 91 were males and 166 were females. In female group, frequency of reduction of flow through right sigmoid sinus is slightly higher than in male group. Frequency of reduction of flow through left sigmoid sinus increase as age increase in male group. In female group frequency of reduction of flow through right sigmoid sinus increase as age increase. In our study, females were more likely to have symmetrical transverse and sigmoid sinuses than males. Males had more hypoplastic left transverse sinus compared to females. Significance of gender difference of intracranial venous sinuses anatomy is not known.
The strength of the present study is large sample size, still retrospective nature of the study is the major limitation. Other limitations are single center study, absence of contrast-enhanced MRV and lack of long term follow up data to look for significance of anatomical variations of MRV. Single center study may cause case selection bias and may miss more variations. Reporting by single radiologist in the present study may also cause bias in the interpretation. Venous flow in the plane of image acquisition may produce saturation and resultant nulling of the venous signal at TOF MR Venography, may lead to misinterpretation of images and diagnosis. Visualization of the dural sinuses is superior with contrast-enhanced MR venography because of a decrease in the effects of turbulent flow. Absence of contrast-enhanced MRV in the present study may overinterpret the flowgaps or other anatomical variations of the dural sinuses. Future prospective studies with contrast-enhanced MRV or autopsy series should be planned to overcome these limitations.

CONCLUSION

Knowledge of anatomical variations of cerebral dural venous sinuses is important. In the absence of this, flow gap in the venous sinus, hypoplasia and aplasia of the transverse sinus may be mistaken for venous sinus thrombosis. Hypoplastic left transverse sinus is the most common anatomical variation in the present study. Hypoplastic left transverse sinus is more common in male compared to female. Other anatomical variations of dural venous sinuses are not significantly differ among both genders. Present study is the largest study from India and first in the literature to study the gender difference of anatomical variations of dural venous sinuses in best of our knowledge. Importance of male predominance of hypoplastic transverse sinus is not clear. Further studies are needed to explore the importance of gender difference of anatomical variations of dural venous sinuses and to confirm the results of present study.

Acknowledgments

We are acknowledging Dr. Rekha Gupta for her help.

References

1. Mattle HP, Wentz KU, Edelman RR, Wallner B, Finn JP, Barnes P, et al. Cerebral venography with MR. Radiology. 1991; 178:453–458. PMID: 1987608.
crossref
2. Ayanzen RH, Bird CR, Keller PJ, McCully FJ, Theobold MR, Heiserman JE. Cerebral MR venography: normal anatomy and potential diagnostic pitfalls. AJNR Am J Neuroradiol. 2000; 21:74–78. PMID: 10669228.
3. Widjaja E, Griffiths PD. Intracranial MR venography in children: normal anatomy and variations. AJNR Am J Neuroradiol. 2004; 25:1557–1562. PMID: 15502138.
4. Liauw L, van Buchem MA, Spilt A, de Bruine FT, van den Berg R, Hermans J, et al. MR angiography of the intracranial venous system. Radiology. 2000; 214:678–682. PMID: 10715029.
crossref
5. Wetzel SG, Kirsch E, Stock KW, Kolbe M, Kaim A, Radue EW. Cerebral veins: comparative study of CT venography with intraarterial digital subtraction angiography. AJNR Am J Neuroradiol. 1999; 20:249–255. PMID: 10094346.
6. Alper F, Kantarci M, Dane S, Gumustekin K, Onbas O, Durur I. Importance of anatomical asymmetries of transverse sinuses: an MR venographic study. Cerebrovasc Dis. 2004; 18:236–239. PMID: 15273441.
crossref
7. Curé JK, Van Tassel P, Smith MT. Normal and variant anatomy of the dural venous sinuses. Semin Ultrasound CT MR. 1994; 15:499–519. PMID: 7880564.
crossref
8. Zouaoui A, Hidden G. Cerebral venous sinuses: anatomical variants or thrombosis? Acta Anat (Basel). 1988; 133:318–324. PMID: 3227793.
crossref
9. Rollins N, Ison C, Booth T, Chia J. MR venography in the pediatric patient. AJNR Am J Neuroradiol. 2005; 26:50–55. PMID: 15661699.
10. Surendrababu NR, Subathira , Livingstone RS. Variations in the cerebral venous anatomy and pitfalls in the diagnosis of cerebral venous sinus thrombosis: low field MR experience. Indian J Med Sci. 2006; 60:135–142. PMID: 16679629.
crossref
11. Sharma UK, Sharma K. Intracranial MR venography using low-field magnet: normal anatomy and variations in Nepalese population. JNMA J Nepal Med Assoc. 2012; 52:61–65. PMID: 23478731.
crossref
12. Kaplan HA, Browder AA, Browder J. Atresia of the rostral superior sagittal sinus: associated cerebral venous patterns. Neuroradiology. 1972; 4:208–211. PMID: 4677615.
crossref
13. Hacker H. Superficial supratentorial veins and dural sinuses. In : Newton TH, Gordon Potts MDD, editors. Radiology of the Skull and Brain: Angiography. St. Louis: C.V. Mosby Company;1974. p. 1851–1902.
14. Kaplan HA, Browder J. Atresia of the rostral superior sagittal sinus: substitute parasagittal venous channels. J Neurosurg. 1973; 38:602–607. PMID: 4711634.
crossref
15. San Millán Ruíz D, Fasel JH, Gailloud P. Unilateral hypoplasia of the rostral end of the superior sagittal sinus. AJNR Am J Neuroradiol. 2012; 33:286–291. PMID: 22051814.
crossref
16. San Millán Ruíz D, Gailloud P, Rufenacht DA, Delaville JH, Henry F, Fasel J. The craniocervical venous system in relation to cerebral venous drainage. AJNR Am J Neuroradiol. 2002; 23:1500–1508. PMID: 12372739.
17. Lang J. The floor of the posterior cranial fossa. clinical Anatomy of the posterior cranial fossa and its foramina. New York: Thieme;1991. p. 6–9.
18. Ruigrok AN, Salimi-Khorshidi G, Lai MC, Baron-Cohen S, Lombardo MV, Tait RJ, et al. A meta-analysis of sex differences in human brain structure. Neurosci Biobehav Rev. 2014; 39:34–50. PMID: 24374381.
crossref
19. Stefani MA, Schneider FL, Marrone ACH, Severino AG. Influence of the gender on cerebral vascular diameters observed during the magnetic resonance angiographic examination of willis circle. Braz Arch Biol Technol. 2013; 56:45–52.
crossref
20. Savelyeva L, Bogomyakova O, Prygova Y, Tulupov A. Anatomic variations of sigmoid sinuses on phase contrast MR-angiography. In : ECR 2012; 2012 March 1 - 5; Vienna, Austria. European Congress of Radiology;2012.
Fig. 1

A. Normal MRV including symmetrical transverse sinuses. B. Hypoplastic left transverse sinus and aplastic left sigmoid sinus (long thin arrow). C. Aplastic right transverse and sigmoid sinus (arrowheads). D. Hypoplastic right transverse sinus (thick arrowhead). E. Aplastic left transverse sinus (long thin arrow) and hypoplastic left sigmoid sinus. F. Aplastic anterior one third superior sagittal sinus (short thin arrows).

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Table 1

Indications for Magnetic Resonance Venography (MRV)

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Indication Male (%) Female (%)
Headache 453 (77.8) 794 (74.1)
Headache and vertigo 67 (11.5) 150 (14.0)
Seizure 23 (4.0) 64 (6.0)
Headache and vomiting 19 (3.3) 34 (3.2)
Vertigo 12 (2.1) 21 (2.0)
Altered sensorium 1 (0.2) 6 (0.6)
Forgetfulness 4 (0.7) 1 (0.1)
Others 3 (0.5) 2 (0.2)
Table 2

Normal Variations of Transverse and Sigmoid Sinuses

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Variation Total (%) Male (%) Female (%) p value
Transverse sinus
 Symmetrical 1106 (66.9) 364 (62.5) 742 (69.2) 0.007
 Left sided hypoplastic 352 (21.3) 145 (24.9) 207 (19.3) 0.009
 Left sided aplastic/Atrectic 67 (4.1) 31 (5.3) 36 (3.4) 0.07
 Right sided Hypoplastic 91 (5.5) 33 (5.7) 58 (5.4) 0.91
 Right sided aplastic/Atrectic 12 (0.7) 4 (0.7) 8 (0.7) 0.87
 Hypoplastic Bilateral Transverse sinuses 26 (1.5) 5 (0.9) 21 (2.0) 0.13
Sigmoid sinus
 Symmetrical 1418 (85.7) 483 (83.0) 935 (87.2) 0.02
 Left sided Hypoplastic 154 (9.4) 66 (11.3) 88 (8.2) 0.05
 Left sided aplastic/atrectic 35 (2.1) 15 (2.6) 20 (1.9) 0.43
 Right sided Hypoplastic 40 (2.4) 17 (2.9) 23 (2.1) 0.42
 Right sided Aplastic/Atrectic 4 (0.2) 1 (0.2) 3 (0.3) 0.92
 Hypoplastic Bilateral Sigmoid sinuses 3 (0.2) 0 (0) 3 (0.3) 0.50
Table 3

Normal Variations of Superior Sagittal Sinus (SSS)

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Total (%) Male Female p value
Normal 1616 (97.7) 569 (97.8) 1047 (97.7) 0.96
Anterior one third hypoplastic 6 (0.4) 3 (0.5) 3 (0.3) 0.74
Atractic anterior one third 15 (0.9) 6 (1.0) 9 (0.8) 0.90
Hypoplastic Anterior Half of SSS 1 (0.1) 0 (0) 1 (0.1) 1.00
Hypoplastic anterior 2/3rd of SSS 3 (0.2) 1 (0.2) 2 (0.2) 0.59
Hypoplastic middle part of SSS 13 (0.7) 3 (0.5) 10 (0.9) 0.53
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