首页> 外文期刊>American journal of rhinology >Septectomy and septal dermoplasty for the treatment of severe transfusion-dependent epistaxis in patients with hereditary hemorrhagic telangiectasia and septal perforation.
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Septectomy and septal dermoplasty for the treatment of severe transfusion-dependent epistaxis in patients with hereditary hemorrhagic telangiectasia and septal perforation.

机译:行隔壁切除术和隔间隔皮成形术治疗严重的输血依赖性鼻出血,用于遗传性出血性毛细血管扩张和隔间隔穿孔。

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BACKGROUND: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by abnormal angiogenesis with resultant telangiectasia formation in mucocutaneous tissues, visceral organs, and the central nervous system. The most common manifestation of HHT is epistaxis resulting from trauma to thin-walled telangiectasias. Many patients with HHT experience worsened epistaxis due to the presence of a septal perforation. Septal perforation in HHT patients results from aggressive noncartilage sparing treatments such as monopolar cauterization. Although the mainstay of treatment for patients with severe transfusion-dependent HHT remains to be septal dermoplasty (SD), patients with a septal perforation are less likely to have a successful outcome. In this small subset of patients, septectomy (ST) combined with SD is proposed to eliminate this variable to improve skin graft uptake and therefore outcome. This study reviews the indications, procedure, and outcome of nine patients with severe transfusion-dependent HHT and septal perforation who underwent the combined procedure of SD/ST. METHODS: Nine HHT patients with severe transfusion-dependent epistaxis and septal perforation underwent SD/ST at our institution over a 5-year period. Quality of life, including number of daily events of epistaxis, and transfusion requirements were determined before and after surgery. Technical aspects of the procedure as well as complications were reviewed. RESULTS: The combined procedure of SD/ST resulted in a long-lasting subjective improvement in quality of life for all patients. Similarly, transfusion requirements were reduced from 22.61 to 9.57 (p < 0.05). There were no complications or increased morbidity from the procedure. CONCLUSION: Combined SD/ST is a safe and effective treatment for HHT patients with transfusion-dependent epistaxis and septal perforation.
机译:背景:遗传性出血性毛细血管扩张(HHT)是一种常染色体显性遗传疾病,其特征在于血管生成异常,并在粘膜皮肤组织,内脏器官和中枢神经系统中形成毛细血管扩张。 HHT最常见的表现是由于对薄壁毛细血管扩张的创伤导致的鼻epi。许多HHT患者由于存在间隔穿孔而使鼻出血恶化。 HHT患者的间隔穿孔是由积极的无软骨保留疗法(例如单极电灼)引起的。尽管严重输血依赖型HHT患者的主要治疗手段仍是隔间隔皮囊成形术(SD),但具有隔间隔穿孔的患者成功治疗的可能性较小。在这一小部分患者中,建议行深隔切除术(ST)与SD结合以消除该变量,从而改善皮肤移植物的摄取并因此改善结局。这项研究回顾了9例接受SD / ST联合手术的严重输血依赖性HHT和间隔穿孔的患者的适应症,手术和结果。方法:9名HHT患者,严重依赖输血的鼻axis和鼻中隔穿孔,在我们机构进行了为期5年的SD / ST。在手术前后确定生活质量,包括每天发生的鼻st事件和输血需求。程序的技术方面以及并发症进行了审查。结果:SD / ST的联合程序导致所有患者生活质量的主观持久改善。同样,输血要求从22.61降至9.57(p <0.05)。该手术没有并发症或发病率增加。结论:SD / STA联合治疗HHT患者输血依赖型鼻中隔穿孔是一种安全有效的方法。

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