Prevalence of Pulmonary Arteriovenous Malformations as Estimated by Low-Dose Thoracic CT Screening

被引:83
作者
Nakayama, Masayuki [1 ,3 ]
Nawa, Takeshi [1 ,4 ]
Chonan, Tatsuya [1 ,5 ]
Endo, Katsuyuki [1 ,6 ]
Morikawa, Satoshi [1 ]
Bando, Masashi [2 ]
Wada, Yasuhiko [7 ]
Shioya, Takanobu [8 ]
Sugiyama, Yukihiko [2 ]
Fukai, Shimao [1 ,9 ]
机构
[1] Hitachi Med Ctr, Thorac CT Screening Grp, Hitachi, Ibaraki, Japan
[2] Jichi Med Univ, Dept Pulm Med, Shimotsuke, Tochigi, Japan
[3] Hitachiomiya Saiseikai Hosp, Dept Internal Med, Hitachiomiya, Ibaraki, Japan
[4] Hitachi Gen Hosp, Dept Pulm Med, Hitachi, Ibaraki, Japan
[5] Nikko Mem Hosp, Dept Med, Tokyo, Japan
[6] Hitachi Gen Hosp, Dept Pulm Surg, Hitachi, Ibaraki, Japan
[7] Kochi Univ, Fac Nutr, Kochi, Japan
[8] Akita Univ, Grad Sch Hlth Sci, Dept Phys Therapy, Akita 010, Japan
[9] Ibarakihigashi Natl Hosp, Natl Hosp Org, Dept Pulm Surg, Ibaraki, Japan
关键词
pulmonary arteriovenous malformations (PAVMs); prevalence; low-dose CT screening; hereditary hemorrhagic telangiectasia (HHT); HEREDITARY HEMORRHAGIC TELANGIECTASIA; LUNG-CANCER; POPULATION;
D O I
10.2169/internalmedicine.51.7305
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background 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. Methods 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. Results 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. Conclusion PAVMs are more prevalent than previously reported, especially among females.
引用
收藏
页码:1677 / 1681
页数:5
相关论文
共 18 条
[1]  
ALLEN SW, 1993, PEDIATR CARDIOL, V14, P58
[2]  
[Anonymous], JSCTS
[3]   Pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia -: A Series of 126 patients [J].
Cottin, Vincent ;
Chinet, Thierry ;
Lavole, Armelle ;
Corre, Romain ;
Marchand, Eric ;
Reynaud-Gaithert, Martine ;
Plauchu, Henri ;
Cordier, Jean-Francois .
MEDICINE, 2007, 86 (01) :1-17
[4]   Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan [J].
Dakeishi, M ;
Shioya, T ;
Wada, Y ;
Shindo, T ;
Otaka, K ;
Manabe, M ;
Nozaki, J ;
Inoue, S ;
Koizumi, A .
HUMAN MUTATION, 2002, 19 (02) :140-148
[5]  
Esplin M S, 1997, Obstet Gynecol Surv, V52, P248, DOI 10.1097/00006254-199704000-00022
[6]   International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia [J].
Faughnan, M. E. ;
Palda, V. A. ;
Garcia-Tsao, G. ;
Geisthoff, U. W. ;
McDonald, J. ;
Proctor, D. D. ;
Spears, J. ;
Brown, D. H. ;
Buscarini, E. ;
Chesnutt, M. S. ;
Cottin, V. ;
Ganguly, A. ;
Gossage, J. R. ;
Guttmacher, A. E. ;
Hyland, R. H. ;
Kennedy, S. J. ;
Korzenik, J. ;
Mager, J. J. ;
Ozanne, A. P. ;
Piccirillo, J. F. ;
Picus, D. ;
Plauchu, H. ;
Porteous, M. E. M. ;
Pyeritz, R. E. ;
Ross, D. A. ;
Sabba, C. ;
Swanson, K. ;
Terry, P. ;
Wallace, M. C. ;
Westermann, C. J. J. ;
White, R. I. ;
Young, L. H. ;
Zarrabeitia, R. .
JOURNAL OF MEDICAL GENETICS, 2011, 48 (02) :73-87
[7]   Transcatheter embolotherapy of maternal pulmonary ateriovenous malformations during pregnancy [J].
Gershon, AS ;
Faughnan, ME ;
Chon, KS ;
Pugash, RA ;
Clark, JA ;
Bohan, MJ ;
Henderson, KJ ;
Hyland, RH ;
White, RI .
CHEST, 2001, 119 (02) :470-477
[8]   Pulmonary arteriovenous malformations - A state of the art review [J].
Gossage, JR ;
Kanj, G .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (02) :643-661
[9]   Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients [J].
Kjeldsen, AD ;
Vase, P ;
Green, A .
JOURNAL OF INTERNAL MEDICINE, 1999, 245 (01) :31-39
[10]   Revisions in the International System for Staging Lung Cancer [J].
Mountain, CF .
CHEST, 1997, 111 (06) :1710-1717