Department of Internal Medicine, Hyogo Prefectural Tamba Medical Center, 2002-7 Iso, Hikami-cho, Tamba, 669-3495, Japan.
Division of Community Medicine and Career Development, Kobe University Graduate School of Medicine, 2-1-5, Arata-cho, Hyogo-ku, Kobe, Hyogo, 652-0032, Japan.
BMC Infect Dis. 2021 Jun 5;21(1):530. doi: 10.1186/s12879-021-06230-4.
Cytomegalovirus (CMV) is reported to have thrombogenic characteristics that activate factor X in vitro and stimulate the production of factor VIII and von Willebrand factor (vWF). Thrombosis associated with CMV infection is prevalent among immunocompromised patients and predominantly presents as a solitary large thrombus in the deep vein, pulmonary artery, splanchnic arteriovenous ducts, or other similar sites. Multiple thrombi, however, are rarely observed in such cases. Here, we report about an immunocompetent man with multiple microthrombi associated with CMV infection.
A 72-year-old Japanese man who complained of abdominal pain was hospitalized with multiple colonic stenosis. He was later diagnosed with CMV enterocolitis and treated with ganciclover from Day 27 post-admission. During hospitalization, the patient developed thrombi in his fingers. He was initially treated with anticoagulant therapy (rivaroxaban); however, the therapy was discontinued owing to a prolonged activated thromboplastin time and an elevated international normalized ratio of prothrombin time. Instead, vitamin K and fresh-frozen plasma were administered. Nevertheless, his coagulation profile remained abnormal. Eventually, he developed colonic perforation and had to undergo emergency surgery. An intraoperative specimen showed several microthrombi in the middle and small arteriovenous ducts of his small and large intestines. The patient's coagulopathy improved preoperatively, and his overall condition improved postoperatively. Since the activation of ADAMTS13 was reduced remarkably, the thrombotic tendency was determined to be a thrombotic microangiopathy-like condition owing to increased vWF. We could not attribute the coagulopathy to any other cause except CMV infection; therefore, we concluded that this was a case of multiple thrombosis associated with CMV.
We present an extremely rare case of a patient with multiple thrombotic microangiopathy-like microthrombosis caused by CMV infection. Our findings suggest that CMV infection may be considered as a differential diagnosis for immunocompetent individuals who present with thrombosis of unspecified cause.
巨细胞病毒(CMV)据报道具有促血栓形成特性,可在体外激活因子 X,并刺激因子 VIII 和血管性血友病因子(vWF)的产生。免疫功能低下患者中与 CMV 感染相关的血栓形成较为常见,主要表现为深静脉、肺动脉、内脏动静脉导管或其他类似部位的单个大血栓。然而,在这种情况下很少观察到多个血栓。在此,我们报告一例免疫功能正常的 CMV 感染相关多发性微血栓形成患者。
一名 72 岁的日本男性因腹痛入院,伴有多处结肠狭窄。入院后他被诊断为 CMV 结肠炎,并于入院后第 27 天开始接受更昔洛韦治疗。住院期间,患者手指出现血栓。他最初接受抗凝治疗(利伐沙班);然而,由于活化部分凝血活酶时间延长和国际标准化比值延长,凝血酶原时间,抗凝治疗被停止。改为给予维生素 K 和新鲜冷冻血浆。然而,他的凝血谱仍异常。最终,他发生结肠穿孔,不得不进行紧急手术。术中标本显示他的小肠和大肠的中小动静脉导管中有几个微血栓。患者的凝血功能障碍在术前得到改善,术后整体情况得到改善。由于 ADAMTS13 的活性显著降低,考虑到 vWF 增加,血栓倾向被确定为血栓性微血管病样情况。除 CMV 感染外,我们无法将凝血障碍归因于任何其他原因;因此,我们认为这是一例由 CMV 感染引起的多发性血栓形成病例。
我们报告了一例极其罕见的由 CMV 感染引起的多发性血栓性微血管病样微血栓形成患者。我们的发现表明,CMV 感染可能被视为原因不明血栓形成的免疫功能正常个体的鉴别诊断。