Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (14)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Bakkaloglu, S. A.
Right arrow Articles by Erdem, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bakkaloglu, S. A.
Right arrow Articles by Erdem, T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrol Dial Transplant (2000) 15: 246-248
© 2000 European Renal Association-European Dialysis and Transplant Association


Case Reports

Cerebral vasculitis in Henoch–Schönlein purpura

Sevcan A. Bakkaloglu1, Mesiha Ekim, Necmiye Tümer1, Gülhis Deda2, Ilhan Erden3 and Tansel Erdem1

1 Departments of Pediatric Nephrology, 2 Pediatric Neurology and 3 Radiology, Ankara University Faculty of Medicine, Ankara, Turkey

Correspondence and offprint requests to: Sevcan A. Bakkaloglu, Baglar caddesi 34/19, 06670 Seyranbaglari, Ankara, Turkey.

Keywords: cerebral vasculitis; Henoch–Schönlein purpura



   Introduction
 
Henoch–Schönlein purpura (HSP) is an immunologically mediated systemic vasculitis of small blood vessels affecting predominantly the skin, gastrointestinal tract, joints, and kidneys [1]. Because of its systemic nature, involvement of other organ systems such as cardiopulmonary, genitourinary, and nervous system may be observed [2–5]. Neurological involvement is more common in HSP than is generally appreciated. Headache and behavioural changes are described in a significant proportion of children with HSP [6], but severe neurological complications are rare during the acute phase of the illness [7–9].

We observed a child with HSP who developed severe . . . [Full Text of this Article]



   Case
 


   Discussion
 


   References
 

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Rheumatology (Oxford)Home page
L. Garzoni, F. Vanoni, M. Rizzi, G. D. Simonetti, B. G. Simonetti, G. P. Ramelli, and M. G. Bianchetti
Nervous system dysfunction in Henoch-Schonlein syndrome: systematic review of the literature
Rheumatology, December 1, 2009; 48(12): 1524 - 1529.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
S. A. Bakkaloglu, C. S. Kasapkara, O. Soylemezoglu, H. Peru, K. Fidan, E. Hasanoglu, and N. Buyan
Successful management of anti-GBM disease in a 51/2-year-old girl
Nephrol. Dial. Transplant., October 1, 2006; 21(10): 2979 - 2981.
[Full Text] [PDF]