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Unique case of acquired pulmonary arteriovenous malformation developed by calcic constrictive pericarditis Toru Inami, 1 Shinya Yokoyama, 1 Yoshihiko Seino, 1 Kyoichi Mizuno 2 1 Cardiovascular Center, Nippon Medical School Chiba-Hokusoh Hospital, Chiba, Japan 2 Department of Cardiovascular Medicine, Nippon Medical School, Tokyo, Japan Correspondence to Dr Toru Inami, [email protected] To cite: Inami T, Yokoyama S, Seino Y, et al. BMJ Case Rep Published online: [ please include Day Month Year] doi:10.1136/ bcr-2012-008345 DESCRIPTION A 58-year-old woman admitted to evaluate the symptoms of right-sided heart failure with slight ascites and peripheral oedema lasting more than 6 months. Her medical history revealed that she had been affected by pleuritis when she was 34 years old, and be diagnosed as constrictive peri- carditis documented by right ventricular pressure tracings showing dip-and-plateau pattern at 50 years. The chest x-ray (lateral view) demon- strated extensive pericardial calcications from the anterior to inferior side of the heart ( gure 1) and newly visible mass in distal site of right middle lobe of lung. The mass had not been detected 2 years before. Three-dimensional reconstruction of CT showed the pulmonary arteriovenous malformation (PAVM) that measured 42×33 mm diameter in distal site of segment 5 ( gure 2 and video 1). PAVM was rst reported by Churton in 1987. 1 More than of PAVMs are congenital, and 60% of congenital have been associated with Osler-Weber-Render disease or herediary haemor- rhaogic telangiecasia. Meanwhile many of acquired PAVMs are associated with the mitral stenosis, of which high pulmonary vascular resistance seems to contribute to the developing of PAVM. Killian reported that pulmonary hypertension was present more than 50% in constrictive pericarditis after cardiac surgery. 2 Pulmonary artery pressure in PAVM is generally normal or low, so PAVM works as a function of low-resistance circuit to evacuate high blood pressure in pulmonary vascular resist- ance with constrictive pericarditis. To the best of our knowledge this case is the rst literature describing acquired PAVM secondary to constrictive pericarditis. Figure 1 Chest x-ray (lateral view) showing extensive circumferential pericardial calcications. Figure 2 Three-dimensional reconstruction of CT illustrates the newly developed pulmonary arteriovenous malformation in distal site of right middle lobe of lung. Inami T, et al. BMJ Case Rep 2013. doi:10.1136/bcr-2012-008345 1 Images in on 1 May 2020 by guest. Protected by copyright. http://casereports.bmj.com/ BMJ Case Reports: first published as 10.1136/bcr-2012-008345 on 15 February 2013. Downloaded from

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  • Unique case of acquired pulmonary arteriovenousmalformation developed by calcific constrictivepericarditisToru Inami,1 Shinya Yokoyama,1 Yoshihiko Seino,1 Kyoichi Mizuno2

    1Cardiovascular Center,Nippon Medical SchoolChiba-Hokusoh Hospital,Chiba, Japan2Department of CardiovascularMedicine, Nippon MedicalSchool, Tokyo, Japan

    Correspondence toDr Toru Inami,[email protected]

    To cite: Inami T,Yokoyama S, Seino Y, et al.BMJ Case Rep Publishedonline: [please include DayMonth Year] doi:10.1136/bcr-2012-008345

    DESCRIPTIONA 58-year-old woman admitted to evaluate thesymptoms of right-sided heart failure with slightascites and peripheral oedema lasting more than

    6 months. Her medical history revealed that shehad been affected by pleuritis when she was34 years old, and be diagnosed as constrictive peri-carditis documented by right ventricular pressuretracings showing dip-and-plateau pattern at50 years. The chest x-ray (lateral view) demon-strated extensive pericardial calcifications from theanterior to inferior side of the heart (figure 1) andnewly visible mass in distal site of right middle lobeof lung. The mass had not been detected 2 yearsbefore. Three-dimensional reconstruction of CTshowed the pulmonary arteriovenous malformation(PAVM) that measured 42×33 mm diameter indistal site of segment 5 (figure 2 and video 1).PAVM was first reported by Churton in 1987.1

    More than of PAVMs are congenital, and 60% ofcongenital have been associated withOsler-Weber-Render disease or herediary haemor-rhaogic telangiecasia. Meanwhile many of acquiredPAVMs are associated with the mitral stenosis, ofwhich high pulmonary vascular resistance seems tocontribute to the developing of PAVM. Killianreported that pulmonary hypertension was presentmore than 50% in constrictive pericarditis aftercardiac surgery.2 Pulmonary artery pressure inPAVM is generally normal or low, so PAVM worksas a function of low-resistance circuit to evacuatehigh blood pressure in pulmonary vascular resist-ance with constrictive pericarditis.To the best of our knowledge this case is the first

    literature describing acquired PAVM secondary toconstrictive pericarditis.

    Figure 1 Chest x-ray (lateral view) showing extensivecircumferential pericardial calcifications.

    Figure 2 Three-dimensional reconstruction of CT illustrates the newly developed pulmonary arteriovenousmalformation in distal site of right middle lobe of lung.

    Inami T, et al. BMJ Case Rep 2013. doi:10.1136/bcr-2012-008345 1

    Images in…

    on 1 May 2020 by guest. P

    rotected by copyright.http://casereports.bm

    j.com/

    BM

    J Case R

    eports: first published as 10.1136/bcr-2012-008345 on 15 February 2013. D

    ownloaded from

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  • Learning points

    ▸ Constrictive pericarditis could be a cause of acquiredpulmonary arteriovenous malformation.

    ▸ The presence of pulmonary arteriovenous malformation(PAVM) should be evaluated in the constrictive pericarditis.This case describes a link between PAVM and constrictivepericarditis.

    Competing interests None.

    Patient consent Obtained.

    Provenance and peer review Not commissioned; externally peer reviewed.

    REFERENCES1 Churton T. Multiple aneurysms of pulmonary artery. BMJ 1897;1:1223.2 Killian DM, Furiasse JG, Scanlon PJ, et al. Constrictive pericarditis after cardiac

    surgery. Am Heart J 1989;118:563–8.

    Copyright 2013 BMJ Publishing Group. All rights reserved. For permission to reuse any of this content visithttp://group.bmj.com/group/rights-licensing/permissions.BMJ Case Report Fellows may re-use this article for personal use and teaching without any further permission.

    Become a Fellow of BMJ Case Reports today and you can:▸ Submit as many cases as you like▸ Enjoy fast sympathetic peer review and rapid publication of accepted articles▸ Access all the published articles▸ Re-use any of the published material for personal use and teaching without further permission

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    Video 1 The newly developed pulmonary arteriovenous malformationwas animated in distal site of right middle lobe of lung.

    2 Inami T, et al. BMJ Case Rep 2013. doi:10.1136/bcr-2012-008345

    Images in…

    on 1 May 2020 by guest. P

    rotected by copyright.http://casereports.bm

    j.com/

    BM

    J Case R

    eports: first published as 10.1136/bcr-2012-008345 on 15 February 2013. D

    ownloaded from

    http://casereports.bmj.com/