Nakayama Masayuki, Nawa Takeshi, Chonan Tatsuya, Endo Katsuyuki, Morikawa Satoshi, Bando Masashi, Wada Yasuhiko, Shioya Takanobu, Sugiyama Yukihiko, Fukai Shimao
Thoracic CT Screening Group, Hitachi Medical Center, Japan.
Intern Med. 2012;51(13):1677-81. doi: 10.2169/internalmedicine.51.7305. Epub 2012 Jul 1.
Pulmonary arteriovenous malformations (PAVMs) are rarely encountered in clinical practice. The prevalence of PAVMs associated with hereditary hemorrhagic telangiectasia (HHT) has been estimated based on the rate in the family members of HHT patients, but the prevalence of PAVMs in the general population remains unknown.
We retrospectively examined the prevalence and clinical characteristics of PAVMs as detected by a low-dose thoracic CT screening program for lung cancer at the Hitachi Medical Center and the Hitachi General Health Care Center in the northern part of Ibaraki Prefecture, Japan.
From 2001 to 2007, we identified eight patients (seven females and one male) with PAVMs among 21,235 initial screening participants (the mean age of the patients with PAVMs and that of the screening participants was 60.6 years). The prevalence of PAVMs was estimated at 38 per 100,000 individuals [95% confidence interval (CI)=18-76]. The diameter of the PAVMs was a mean of 6.6 mm, and none of the lesions could be detected by chest X-ray. Females older than 60 years tended to have larger PAVMs than younger women did (p=0.06). Two patients (25%) were diagnosed with HHT. One patient had previously undergone surgery for a brain abscess.
PAVMs are more prevalent than previously reported, especially among females.
肺动静脉畸形(PAVM)在临床实践中很少见。与遗传性出血性毛细血管扩张症(HHT)相关的PAVM患病率是根据HHT患者家庭成员中的发病率估算的,但一般人群中PAVM的患病率仍不清楚。
我们回顾性研究了日本茨城县北部日立医疗中心和日立综合医疗中心通过低剂量胸部CT肺癌筛查项目检测到的PAVM的患病率和临床特征。
2001年至2007年,在21235名初次筛查参与者中,我们识别出8例PAVM患者(7例女性和1例男性)(PAVM患者和筛查参与者的平均年龄为60.6岁)。PAVM的患病率估计为每10万人中有38例[95%置信区间(CI)=18 - 76]。PAVM的直径平均为6.6毫米,胸部X线检查均未发现这些病变。60岁以上女性的PAVM往往比年轻女性更大(p = 0.06)。2例患者(25%)被诊断为HHT。1例患者曾因脑脓肿接受手术。
PAVM比先前报道的更为普遍,尤其是在女性中。