Al-Jafar Hassan, Al-Barjas H, Hashem Raed A, Refaii Thanaa M K, AlSaeed Ahmad M
Department of Hematology, Amiri Hospital, Kuwait City, Kuwait.
Department of Surgery, Amiri Hospital, Kuwait City, Kuwait.
Int J Surg Case Rep. 2014;5(12):1186-9. doi: 10.1016/j.ijscr.2014.09.039. Epub 2014 Oct 31.
Acquired bleeding disorders are rare and may be missed before surgery. Additionally, they may be refractory to conventional treatments.
A 50-year-old patient experienced prolonged post-operative bleeding when his bleeding disorder was missed prior to his undergoing inguinal herniorrhaphy. Post-operative investigations revealed severe acquired von Willebrand syndrome associated with a monoclonal gammopathy of undetermined significance. A few months later, he required umbilical herniorrhaphy, but he did not respond to attempts to raise his von Willebrand factor antigen and activity levels using conventional therapies, including desmopressin, cryoprecipitate, intravenous immunoglobulin, and Von Willebrand factor concentrate. A triple therapy combination of dexamethasone, intravenous immunoglobulin, and mycophenolate mofetil was administered, with a successful and sustained response, lasting about 2 months. The surgery was performed safely, without any complications.
Conventional acquired von Willebrand syndrome treatment is usually aimed at replacing von Willebrand factor or stimulating its secretion from storage in endothelial cells. In the present case, the alternative treatment was directed against both the humoral and cell-mediated immune mechanisms.
This case of acquired bleeding disorder showed that more attention must be given to a patient's coagulation profile, even if only very minor laboratory coagulation derangements are detected prior to surgery, to avoid missing such rare disorders. The described triple therapy demonstrated good effects and may be considered for inclusion in a controlled randomized study to determine its usefulness for other surgeries delayed due to severe acquired bleeding disorders. To the best of our knowledge, this triple combination treatment has not been previously used for the treatment of severe acquired bleeding disorders that are refractory to conventional therapies.
获得性出血性疾病较为罕见,术前可能被漏诊。此外,它们可能对传统治疗无效。
一名50岁患者在接受腹股沟疝修补术前其出血性疾病被漏诊,术后出现长时间出血。术后检查发现严重的获得性血管性血友病综合征,伴有意义未明的单克隆丙种球蛋白病。几个月后,他需要进行脐疝修补术,但使用包括去氨加压素、冷沉淀、静脉注射免疫球蛋白和血管性血友病因子浓缩物在内的传统疗法提高其血管性血友病因子抗原和活性水平的尝试均未成功。给予地塞米松、静脉注射免疫球蛋白和霉酚酸酯的三联疗法,获得了成功且持续的反应,持续约2个月。手术安全进行,无任何并发症。
传统的获得性血管性血友病综合征治疗通常旨在替代血管性血友病因子或刺激其从内皮细胞储存中分泌。在本病例中,替代治疗针对体液免疫和细胞介导的免疫机制。
该例获得性出血性疾病表明,即使术前仅检测到非常轻微的实验室凝血异常,也必须更加关注患者的凝血状况,以避免漏诊此类罕见疾病。所描述的三联疗法显示出良好效果,可考虑纳入对照随机研究,以确定其对因严重获得性出血性疾病而推迟的其他手术的有效性。据我们所知,这种三联组合治疗此前尚未用于治疗对传统疗法无效的严重获得性出血性疾病。