home : about us : ahead of print : current issue : archives search instructions : subscriptionLogin 
Users online: 3      Small font sizeDefault font sizeIncrease font size Print this page Email this page


 
CASE REPORT
Year : 2010  |  Volume : 5  |  Issue : 1  |  Page : 39-41
 

Sinus pericranii presenting with macrocephaly and mental retardation


Department of Radiology and Neurosurgery, BGS Global Hospital, Uttarahalli Road, Kengeri, Bangalore - 560 098, India

Date of Web Publication22-Jul-2010

Correspondence Address:
N K Venkataramana
Department of Radiology and Neurosurgery, BGS Global Hospital, Uttarahalli Road, Kengeri, Bangalore - 560 098, Karnataka
India
Login to access the Email id


DOI: 10.4103/1817-1745.66665

PMID: 21042507

Get Permissions

 

   Abstract 

We present a rare case of right parietal sinus pericranii in a 2-year-old female child who presented with a compressible swelling on the right side of the scalp since 3 months of age, with a large head. Magnetic resonance imaging along with venography and conventional angiogram was performed, which confirmed the diagnosis.


Keywords: Digital subtraction angiography, macrocephaly, magnetic resonance imaging, sinus pericranii


How to cite this article:
Kamble R B, Venkataramana N K, Naik L, Shailesh, Shetty R. Sinus pericranii presenting with macrocephaly and mental retardation. J Pediatr Neurosci 2010;5:39-41

How to cite this URL:
Kamble R B, Venkataramana N K, Naik L, Shailesh, Shetty R. Sinus pericranii presenting with macrocephaly and mental retardation. J Pediatr Neurosci [serial online] 2010 [cited 2014 Oct 25];5:39-41. Available from: http://www.pediatricneurosciences.com/text.asp?2010/5/1/39/66665



   Introduction Top


Sinus pericranii is a rare congenital vascular anomaly, which is a fluctuating, compressible venous scalp mass that connects directly to the intracranial dural sinuses through dilated diploic and emissary veins. [1] This anomaly can be readily diagnosed by radiological investigations. Findings on imaging, like magnetic resonance (MR) venography, have already been described. [2] We report a case of sinus pericranii in a 2-year-old female child with a unique presentation of scalp swelling, macrocephaly and mental retardation along with MR imaging (MRI), MR venography and conventional angiographic findings.


   Case Report Top


This 2-year-old girl child born to nonconsanguineous parents presented with a history of large head and an abnormal compressible swelling on the right side of the scalp when she was 3 months old [Figure 1]. The swelling increased in size when the child cried. On examination, the child was found to have macrocephaly with delayed milestone in the form of neck holding at 1 year and standing with support at 22 months. On physical examination, there was a large compressible bluish scalp mass on the right parietal region with bony dents underneath. The mass was seen to increase in size on crying. The anterior and posterior fontanelles were open. The child underwent MRI along with MR venography and digital subtraction angiography (DSA) to confirm diagnosis. MRI showed a T1-hypointense swelling in the right parietal region with bony defect communicating with the superior sagittal sinus and ventricular dilatation [Figure 2]. MR venography showed a dilated large extracranial vein on the right parietal region communicating with the superior sagittal sinus through dilated diploic and emissary veins [Figure 3]. MR angiography was normal [Figure 4]. Subsequently, the child underwent DSA under general anesthesia, which confirmed large extracranial scalp vein draining into the superior sagittal sinus seen on the venous phase. Bilateral internal and external carotid arteries were normal. No dural arteriovenous fistula was found [Figure 5]. Thus, the diagnosis of sinus pericranii was made depending on MR and DSA findings. The child was kept on follow-up.

Sinus pericranii is a rare congenital venous anomaly, which is soft and compressible scalp mass that connects directly to the intracranial dural sinuses through dilated diploic and emissary veins. They are known to increase in size on valsalva manoeuvre or raised intracranial pressures and reduce on nondependent positions. [1] Mainly congenital, traumatic and spontaneous causes are described for the development of sinus pericranii. Traumatic cause is mainly due to tearing of emissary veins and later developing into communicating blood cyst. [1] Pathologically, they can be termed congenital if lined by endothelium. [3] Sinus pericranii can appear at any age, usually <30 years, common in males and, although usually asymptomatic, may present with nausea, vomiting and vertigo. [2],[4] Differential diagnosis for sinus pericranii includes dural fistula, arteriovenous malformation and other midline masses of scalp-like dermoid, lipoma and encephalocele. [4] Sometimes, it can mimic subepicranial varix where there is dilated venous sac on the scalp without communication with intracranial dural sinuses. [5] Sinus pericranii may be associated with various other anomalies, like systemic angiomas and craniosynostosis. [6],[7] It can be diagnosed by clinical examination and radiological imaging. Usefulness of MR venography and computed tomography angiography has already been described to confidently diagnose sinus pericranii and exclude other mimicking causes of scalp swelling. However, conventional angiography may still be useful to rule out other vascular malformations like dural fistula and arteriovenous malformation. Demonstration of extracranial venous sac communicating with intracranial dural sinus via diploic or emissary veins is necessary for the diagnosis of sinus pericranii, which can be easily performed by today's imaging modalities. [2],[5]

The present case showed a large head with developmental delay. Imaging showed mild hydrocephalus. Most of the cases described in the literature are associated with craniosynostosis; however, our case showed macrocephaly. Presence of macrocephaly may be due to hydrocephalus. Developmental delay may be attributed to increased venous pressure in the dural sinuses causing raised intracranial pressures leading to delayed development. Development of transient venous hypertension by sinus pericranii has been described previously. [8]

Treatment options in symptomatic patients include surgical resection or a transvenous endovascular approach. If treatment has to be contemplated, then Gondolfo et al. have recommended to assess the drainage pattern of sinus pericranii. If sinus pericranii is dominant, i.e. if drainage of the brain is through sinus pericranii bypassing the usual venous outlets, then treatment should be avoided. [9] However, spontaneous regression of sinus pericranii has also been reported. [10] Our case was kept on follow-up under close observation to be treated later if the clinical condition worsened.


   Conclusion Top


Sinus pericranii can also be associated with macrocephaly and developmental delay due to possible venous hypertension, which was not described before.

 
   References Top

1.Bollar A, Allut AG, Prieto A, Gelabert M, Becerra E. Sinus pericranii: radiological and etiopathological considerations. J Neurosurg 1992;77:469-72.  Back to cited text no. 1  [PUBMED]  [FULLTEXT]  
2.Azusawa H, Ozaki Y, Shindoh N, Sumi Y. Usefulness of MR Venography in Diagnosing Sinus Pericranii: Case Report. Radiat Med 2000;18;249-52.  Back to cited text no. 2      
3.Cohn I. Sinus pericranii: Report of a case, review of literature. Surg Gynecol Obstet 1926;42:614-24.  Back to cited text no. 3      
4.Sadler LR, Tarr RW, Jungreis CA, Sekhar L. Sinus pericranii: CT and MR findings. J Comput Assist Tomogr 1990;14:124-7.  Back to cited text no. 4  [PUBMED]    
5.Asano K, Sobata E, Kubo O. Subepicranial varix mimicking sinus pericranii: usefulness of three-dimensional computed tomography angiography and bone window computed tomography--case report. Neurol Med Chir (Tokyo) 2000;40:467-71.  Back to cited text no. 5  [PUBMED]  [FULLTEXT]  
6.Nakasu Y, Nakasu S, Minouchi K, Handa J. Multiple sinus pericranii with systemic angiomas: case report. Surg Neurol 1993;39:41-5.  Back to cited text no. 6  [PUBMED]    
7.Mitsukawa N, Satoh K, Hayashi T, Furukawa Y, Suse T, Uemura T, et al. Sinus pericranii associated with craniosynostosis. J Craniofac Surg 2007;18:78-84.  Back to cited text no. 7  [PUBMED]  [FULLTEXT]  
8.Anegawa S, Hayashi T, Torigoe R, Nakagawa S, Ogasawara T. Sinus pericranii with severe symptom due to transient disorder of venous return--case report. Neurol Med Chir (Tokyo) 1991;31:287-9.  Back to cited text no. 8  [PUBMED]  [FULLTEXT]  
9.Gandolfo C, Krings T, Alvarez H, Ozanne A, Schaaf M, Baccin CE, et al. Sinus pericranii: diagnostic and therapeutic considerations in 15 patients. Neuroradiology 2007;49:505-14.  Back to cited text no. 9  [PUBMED]  [FULLTEXT]  
10.Rozen WM, Joseph S, Lo PA. Spontaneous involution of two sinus pericranii - a unique case and review of the literature. J Clin Neurosci 2008;15:833-5.  Back to cited text no. 10  [PUBMED]  [FULLTEXT]  


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]


This article has been cited by
1 Sinus Pericranii: A Case Report and Review of Literature
Shraddha Bhutada,M. R. Lokeshwar,Ashwin Pandey,Makarand Kulkarni
The Indian Journal of Pediatrics. 2012; 79(11): 1523
[Pubmed]
2 Sinus pericranii: A case report and review of literature
Bhutada, S. and Lokeshwar, M.R. and Pandey, A. and Kulkarni, M.
Indian Journal of Pediatrics. 2012; 79(11): 1523-1525
[Pubmed]



 

Top
Print this article  Email this article
Previous article Next article

    

 
  Search
 
   Next article
   Previous article 
   Table of Contents
  
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Article in PDF (1,048 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
    Introduction
    Case Report
    Conclusion
    References
    Article Figures

 Article Access Statistics
    Viewed2094    
    Printed93    
    Emailed1    
    PDF Downloaded113    
    Comments [Add]    
    Cited by others 2    

Recommend this journal