Sturge-Weber Syndrome with Port Wine Stain and Bilateral Choroid Plexus Angiomas: A Case Report

Authors

  • Kaleem Ahmad B.P. Koirala Institute of Health Sciences, Dharan
  • Sajid Ansari B.P. Koirala Institute of Health Sciences, Dharan
  • Kanchan Dhungel B.P. Koirala Institute of Health Sciences, Dharan
  • Mukesh Kumar Gupta B.P. Koirala Institute of Health Sciences, Dharan
  • Ashok Raj Pant B.P. Koirala Institute of Health Sciences, Dharan
  • R K Rauniyar B.P. Koirala Institute of Health Sciences, Dharan

DOI:

https://doi.org/10.3329/jom.v15i1.19877

Keywords:

Sturge-Weber Syndrome, Phakomatosis, Neurocutaneous Syndrome, Computed tomography

Abstract

Sturge-Weber syndrome is a rarenon-hereditary condition characterized by a hamartomatous vascular proliferation. It is usually unilateral; bilateral involvement is seen only in 15% cases. We report a case of a 6 month old male child with Sturge-Weber syndrome with its inherent clinical features and typical imaging findings.

DOI: http://dx.doi.org/10.3329/jom.v15i1.19877

J Medicine 2014; 15: 68-70

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Author Biographies

Kaleem Ahmad, B.P. Koirala Institute of Health Sciences, Dharan

Associate Professor, Department of Radiodiagnosis

Sajid Ansari, B.P. Koirala Institute of Health Sciences, Dharan

Senior Resident, Department of Radiodiagnosis


Kanchan Dhungel, B.P. Koirala Institute of Health Sciences, Dharan

Associate Professor, Department of Radiodiagnosis


Mukesh Kumar Gupta, B.P. Koirala Institute of Health Sciences, Dharan

Associate Professor, Department of Radiodiagnosis

Ashok Raj Pant, B.P. Koirala Institute of Health Sciences, Dharan

Junior Resident, Department of Radiodiagnosis

R K Rauniyar, B.P. Koirala Institute of Health Sciences, Dharan

Professor, Department of Radiodiagnosis

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Published

2014-08-06

How to Cite

Ahmad, K., Ansari, S., Dhungel, K., Gupta, M. K., Pant, A. R., & Rauniyar, R. K. (2014). Sturge-Weber Syndrome with Port Wine Stain and Bilateral Choroid Plexus Angiomas: A Case Report. Journal of Medicine, 15(1), 68–70. https://doi.org/10.3329/jom.v15i1.19877

Issue

Vol. 15 No. 1 (2014)

Section

Case Reports

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