Shah Rahul K, Dhingra Jagdish K, Shapshay Stanley M
Department of Otolaryngology-Head and Neck Surgery, Tufts University School of Medicine, New England Medical Center, Boston, MA 02111, USA.
Laryngoscope. 2002 May;112(5):767-73. doi: 10.1097/00005537-200205000-00001.
OBJECTIVES/HYPOTHESIS: Hereditary hemorrhagic telangiectasia has long been viewed as a rare condition. Recent evidence indicates that the disorder is more frequent than previously thought. Recalcitrant epistaxis is a salient feature of this disease, and the otolaryngologist is often called on to make the diagnosis and guide the primary management of patients with hereditary hemorrhagic telangiectasia. Wider recognition of this condition, awareness of the natural history and associated findings, appropriate workup and screening for arteriovenous malformations (lungs, brain, liver), and knowledge of appropriate interventions can help avoid the considerable morbidity associated with hereditary hemorrhagic telangiectasia.
Retrospective review.
Records of patients treated by the senior author (S.M.S.) for hereditary hemorrhagic teleangiectasia from 1993 to 2000 were reviewed.
Seventy-six patients were identified, 98% of whom had epistaxis as their presenting complaint, with 75% having a family history of hereditary hemorrhagic telangiectasia. The severity of epistaxis varied in the patients: 66% had mild, 21% moderate, and 13% severe epistaxis. Sixty-four percent of patients had no transfusions, 25% had 1 to 10 transfusions, and 11% of patients had more than 10 transfusions. Complications of hereditary hemorrhagic telangiectasia were documented in 30% of patients. Screening for arteriovenous malformations was performed in only 34% of patients. Eighty-two percent of patients received a variable number of Nd:YAG laser treatments.
The study presents the largest retrospective review of patients treated for hereditary hemorrhagic telangiectasia by a single otolaryngologist. The importance of a multidisciplinary approach facilitated by the otolaryngologist for evaluation of concomitant complications and morbidity (arteriovenous malformations) from hereditary hemorrhagic telangiectasia is demonstrated. An algorithm for controlling the epistaxis is presented.
目的/假设:遗传性出血性毛细血管扩张症长期以来一直被视为一种罕见疾病。最近的证据表明,该疾病比以前认为的更为常见。顽固性鼻出血是这种疾病的一个显著特征,耳鼻喉科医生经常被要求对遗传性出血性毛细血管扩张症患者进行诊断并指导其初步治疗。对这种疾病的更广泛认识、对其自然病史和相关发现的了解、对动静脉畸形(肺、脑、肝)的适当检查和筛查,以及对适当干预措施的了解,有助于避免与遗传性出血性毛细血管扩张症相关的相当高的发病率。
回顾性研究。
回顾了1993年至2000年由资深作者(S.M.S.)治疗的遗传性出血性毛细血管扩张症患者的记录。
共确定了76例患者,其中98%以鼻出血为主要症状,75%有遗传性出血性毛细血管扩张症家族史。患者鼻出血的严重程度各不相同:66%为轻度,21%为中度,13%为重度。64%的患者未接受输血,25%的患者接受了1至10次输血,11%的患者接受了超过10次输血。30%的患者记录了遗传性出血性毛细血管扩张症的并发症。仅34%的患者进行了动静脉畸形筛查。82%的患者接受了不同次数的Nd:YAG激光治疗。
该研究是对由一名耳鼻喉科医生治疗的遗传性出血性毛细血管扩张症患者进行的最大规模回顾性研究。证明了由耳鼻喉科医生推动的多学科方法对于评估遗传性出血性毛细血管扩张症的伴随并发症和发病率(动静脉畸形)的重要性。提出了一种控制鼻出血的算法。