Sturge-Weber syndrome-A Case report

Authors

  • Abdul Halim Assistant Professor, Department of Medicine, Noakhali Medical College, Noakhali
  • Md Towhid Alam Assistant Professor, Dept. of Medicine, FMC, Faridpur.
  • RC Barman Assistant Professor, Dept. of Respiratory Medicine, FMC, Faridpur

DOI:

https://doi.org/10.3329/fmcj.v8i1.16899

Keywords:

Sturge-weber syndrome, cuntaneous haemangioma, left sided hemiplegin, epilepsy, intracranial calcification

Abstract

Sturge-weber syndrome is a disease characterized by capillary or cavernous haemangionsm (Port-wine stain) along the cutaneous division of Trigennial nerve. There is venous haemangionsm in subjacent leptomeninges, which may spread causing atrophy of cortex. The patient Md. Zobair Hossain, 11 years old boy, nondiabetic, nonhypertensive presented to us on 20.05.2011 with the complaints of repeated bleeding from a swelling over the outer aspect of right eye ball for 1 month, weakness of left half of body for 1 year and repeated convulsion for 7 years. Diagnosis was confirmed vy CT scan of brain. Through treatment is unsatisfactory, he was advised for laser theraphy for coetaneous lesion and anti-convulsant drug epilepsy.

DOI: http://dx.doi.org/10.3329/fmcj.v8i1.16899

Faridpur Med. Coll. J. 2013;8(1): 44-45

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Published

2013-11-07

How to Cite

Halim, A., Alam, M. T., & Barman, R. (2013). Sturge-Weber syndrome-A Case report. Faridpur Medical College Journal, 8(1), 44–45. https://doi.org/10.3329/fmcj.v8i1.16899

Issue

Vol. 8 No. 1 (2013)

Section

Case Reports