Hemophilia & Coagulation DisordersArchives
Venous thromboembolism in patients undergoing pancreatic cancer surgery (PaTR-VTE) with curative intent; protocol of a prospective observational study
Cancer-associated thrombosis (CAT) is the second most common cause of death in oncology patients after the progression of the tumour itself. This patient group has an increased risk of both venous (4–20%) and arterial (2–5%) thromboembolic events. Cancer is probably the most important acquired...
Bilateral total knee replacement for hemophilic arthropathy: a case report
Von Willebrand disease (vWD) is a congenital bleeding disorder that affects approximately 0.6–1.3% of the population [1]. The etiology of vWD is rooted in the deficiency (Type 1), dysfunction (Type 2), or virtually near absence (Type 3) of von Willebrand factor (vWF) [2], predominantly manifesting...
The prediction of haemophilic arthropathy progression based on MRI findings and clinical characteristics
Haemophilia is a lifelong condition characterized by spontaneous or minor trauma-induced bleeding due to a deficiency in clotting factors, with joint haemorrhage being the most common manifestation. Repeated joint bleeding leads to pain, deformities, and functional impairments, ultimately leading to...
Clinical characteristics and outcomes of disseminated intravascular coagulation in patients with severe fever with thrombocytopenia syndrome
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging zoonosis caused by a novel bunyavirus (SFTS virus, SFTSV), which was initially reported in China in 2009 [1], and emerged in Korea [2], Japan [3], and Vietnam [4]. Currently, SFTSV is mainly transmitted through tick bites [5]. In addition,...
