Management of patient with Sturge-Weber syndrome: a case report. - Suppr | 超能文献

Management of patient with Sturge-Weber syndrome: a case report.

作者信息

Govori Valbona, Gjikolli Bujar, Ajvazi Halil, Morina Nada

机构信息

Neurology Clinic, University Clinical Center of Kosova, Prishtina, Republic of Kosova.

出版信息

Cases J. 2009 Dec 23;2:9394. doi: 10.1186/1757-1626-2-9394.

DOI:10.1186/1757-1626-2-9394

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2806399/

Abstract

INTRODUCTION

Sturge-Weber syndrome sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder.

CASE PRESENTATION

This is case report of a 18-year-old mentally disabled boy, with long-standing seizures, with a port-wine nevi on the left side of the face along the distribution of trigeminal nerve. Interictal encephalogram showed bilateral slow activity, pronounced in the left hemisphere, with epileptogenic activity in the left temporo-parietal region. Skull radiograph, computerized tomography and magnetic resonance imaging showed intracranial calcifications and atrophy of the left brain hemisphere.

CONCLUSION

Professional counseling and support in addition to drug treatment can provide help to patients and their family to overcome their problems and improve the treatment outcome.

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/532c/2806399/0a4639fb84c5/1757-1626-2-9394-1.jpg

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