Inhibitorentwicklung nach früher hoher Exposition und Hirnblutung
Moorthi, C.; Bade, A.; Niekrens, C.; Auerswald, G.; Haubold, K. · Zeitschrift für Orthopädie und Unfallchirurgie · 2010 · Heft S 01 · S. S115-S118
Bibliografische Angaben
Zusammenfassung
SummarySevere haemophilia A was diagnosed postpartum in a newborn. The mother was known as a conductor (intron 22 inversion) and an uncle had a persistently high titer inhibitor after failed ITI.Due to a cephalhaematoma, a high-dose pdFVIII substitution was given within the first days after birth. At the age of six month a severe cerebral haemorrhage occurred, making a high-dose pdFVIII substitution and neurosurgical intervention necessary. Several days later a porth-a-cath-system was implanted. The development of a high titer inhibitor occured six days later, an ITI was started according to the Bonn Protocol. I…