Neuropediatrics 2008; 39(2): 131-133
DOI: 10.1055/s-2008-1077088
Short Communication

© Georg Thieme Verlag KG Stuttgart · New York

Cerebral Sinus Thrombosis in a Patient with Humoral Immunodeficiency on Intravenous Immunoglobulin Therapy: A Case Report

W. Barada 1 , S. Muwakkit 2 , R. Hourani 3 , M. Bitar 4 , M. Mikati 4
  • 1Neurology Division, Internal Medicine Department, American University of Beirut Medical Center, Beirut, Lebanon
  • 2Children Cancer Center of Lebanon, Department of Pediatrics, American University of Beirut Medical Center, Beirut, Lebanon
  • 3Radiology Department, American University of Beirut Medical Center, Beirut, Lebanon
  • 4Pediatrics and Adolescents Medicine Department, American University of Beirut Medical Center, Beirut, Lebanon
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Publikationsverlauf

received 20.02.2008

accepted after revision 14.04.2008

Publikationsdatum:
31. Juli 2008 (online)

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Abstract

We present the case of an 11-year-old boy with humoral immunodeficiency on monthly intravenous immunoglobulins (IVIG) infusions, evaluated for recurrent, brief, neurological deficits secondary to cerebral sinus thrombosis without any identifiable hypercoagulability state. Etiologic possibilities for the thrombotic event are presented with special discussion of IVIG-related cerebral thrombosis. To the best of our knowledge, our patient represents the first reported case of Bruton's disease on IVIG therapy developing a cerebral ischemic event and the second reported case of cerebral sinus thrombosis associated with IVIG use for any disease. Potential concerns regarding the risk of cerebral thrombosis during IVIG therapy in this and other disorders are reviewed.

References

Correspondence

W. BaradaMD 

Neurology Division

Internal Medicine Department

American University of Beirut Medical Center

P. O. Box: 113-6044

Beirut

Lebanon

Fax: +961/1/37 08 02

eMail: wb13@aub.edu.lb