Skip to main navigation Skip to search Skip to main content

Cerebral thromboembolism due to antithrombin III deficiency in two children

  • P. P. Vomberg
  • , C. Breederveld
  • , P. Fleury
  • , W. F. M. Arts
  • Amsterdam UMC - University of Amsterdam

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Despite numerous well-described causes of stroke in infancy and childhood, a significant proportion remains unexplained. Venous thromboembolism is a common complication in adult patients undergoing surgery, and after severe trauma, but not in otherwise healthy children less than 10 years old. However, it may also occur spontaneously without recognizable cause. It has been known for a long time that some patients are particularly prone to venous thrombosis and in recent years efforts have been made to identify the risk factors. The attention of haematologists has been focused on the possibility that certain abnormalities of coagulation may be associated with a tendency to thrombosis, but only in a few instances a clear causal relationship has been established. One such example is a deficiency of antithrombine III, but such a deficiency has hitherto been recognized as a cause for thrombosis in children only in very particular circumstances. We present two young children with stroke of which one was purely ischemic and the other ischemic with secondary hemorrhage. Both our patients showed an AT III deficiency. Patient one also had a cyanotic congenital heart disease with right to left shunting which made cerebral embolism originating from a thrombus in the iliac vein possible to occur. We consider her hematocrit values too low to be a predisposing factor from this thrombosis. AT III deficiency may be caused by several different mechanisms. Either it exists as a congenital (hereditary) or as an acquired disorder. In patient two the family history was positive for hereditary AT III deficiency. However, in patient one, abnormal values for AT III were not present in her family members, nor was a history of thromboembolic disease. All causes for acquired AT III deficiency could be excluded. We conclude that in both children congenital AT III deficiency was the cause of severe thromboembolic complications.
Original languageEnglish
Pages (from-to)42-44
JournalNeuropediatrics
Volume18
Issue number1
DOIs
Publication statusPublished - 1987
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Cerebral thromboembolism due to antithrombin III deficiency in two children'. Together they form a unique fingerprint.

Cite this