Han P, Lou J, Wong H B
Department of Paediatrics, National University of Singapore.
Aust Paediatr J. 1987 Aug;23(4):253-5. doi: 10.1111/j.1440-1754.1987.tb00262.x.
A young infant with Wilms' tumour was found to have acquired von Willebrand's syndrome but no bleeding symptoms. Neither parent of the infant had evidence of von Willebrand's syndrome. Postoperatively, after removal of the tumour, factor VIII complex levels returned to normal. The mechanism of the acquired von Willebrand's syndrome was unclear. No evidence was found of an inhibitor of factor VIII complex or entrapment of factor VIII in the tumour.
一名患有肾母细胞瘤的幼儿被发现患有获得性血管性血友病综合征,但无出血症状。该幼儿的父母均无血管性血友病综合征的证据。术后,肿瘤切除后,凝血因子VIII复合物水平恢复正常。获得性血管性血友病综合征的机制尚不清楚。未发现凝血因子VIII复合物抑制剂或凝血因子VIII在肿瘤中潴留的证据。