Crossette-Thambiah Christina, Randi Anna M, Laffan Michael
Centre for Haematology, Department of Immunology and Inflammation, Imperial College London, UK; Department of Haematology, Imperial College Healthcare NHS Trust, London.
National Heart and Lung Institute, Imperial College.
Haematologica. 2025 Mar 1;110(3):588-595. doi: 10.3324/haematol.2024.285244.
Bleeding in the gastrointestinal tract in patients with von Willebrand disease continues to pose a therapeutic challenge for clinicians. It is associated with significant morbidity and mortality and represents the major unmet need in this disease. Defective angiogenesis in the gut is primarily responsible, resulting in angiodysplastic malformations making bleeding notoriously refractory to standard replacement therapy. A substantial body of evidence now shows that von Willebrand factor has a role in the regulation of angiogenesis but the mechanisms responsible for the formation of vascular malformations remain incompletely understood. Data from the wider field of vascular malformations may lend insight and point to novel therapeutic approaches. Here we review evidence linking von Willebrand factor to angiodysplasia, the associated molecular mechanisms and the implications for therapy.
血管性血友病患者的胃肠道出血对临床医生来说仍然是一个治疗挑战。它与显著的发病率和死亡率相关,是这种疾病中主要未得到满足的需求。肠道血管生成缺陷是主要原因,导致血管发育异常畸形,使得出血对标准替代疗法具有 notoriously refractory(此处疑有误,可能是“ notoriously refractory”,意为“ notoriously难治的”)。大量证据表明血管性血友病因子在血管生成调节中起作用,但血管畸形形成的机制仍未完全了解。来自更广泛血管畸形领域的数据可能会提供见解并指向新的治疗方法。在这里,我们综述了将血管性血友病因子与血管发育异常联系起来的证据、相关分子机制及其对治疗的影响。