Literature DB >> 6732339

Pneumothorax in the Marfan syndrome: prevalence and therapy.

J R Hall, R E Pyeritz, D L Dudgeon, J A Haller.   

Abstract

At least twenty-four reports of pneumothorax associated with the Marfan syndrome have appeared in the medical literature, but the frequency and optimal method of treatment remain unclear. We conducted a retrospective review of medical records from one genetics clinic and found that the frequency of spontaneous pneumothorax in patients older than 12 years with Marfan's syndrome was 4.4% (11 out of 249). Men were more commonly, but no more severely, affected than women. Seven patients had recurrent or bilateral pneumothorax. In 9 of the 11 patients, apical bullae were present and detectable on chest radiograph. Pneumothorax frequently recurred if not treated by resection of the offending bullae. We recommend that all adolescent and adult patients with the Marfan syndrome undergo chest radiography for ascertainment of the gross pathological condition of the lung. Definitive surgical treatment should be performed at the first occurrence of pneumothorax because of the high rate of recurrence after treatment with a chest tube, with or without pleurodesis.

Entities:  

Mesh:

Year:  1984        PMID: 6732339     DOI: 10.1016/s0003-4975(10)61142-3

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  19 in total

1.  Spontaneous pneumothorax as manifestation of Marfan syndrome.

Authors:  Carolina Viveiro; Patricia Rocha; Cristiana Carvalho; Maria Manuel Zarcos
Journal:  BMJ Case Rep       Date:  2013-12-05

Review 2.  Marfan syndrome.

Authors:  J R Gray; S J Davies
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

Review 3.  Spontaneous pneumothorax in diffuse cystic lung diseases.

Authors:  Joseph Cooley; Yun Chor Gary Lee; Nishant Gupta
Journal:  Curr Opin Pulm Med       Date:  2017-07       Impact factor: 3.155

Review 4.  The Genetics of Pneumothorax.

Authors:  Philip M Boone; Rachel M Scott; Stefan J Marciniak; Elizabeth P Henske; Benjamin A Raby
Journal:  Am J Respir Crit Care Med       Date:  2019-06-01       Impact factor: 21.405

Review 5.  Non-cardiac manifestations of Marfan syndrome.

Authors:  Anne H Child
Journal:  Ann Cardiothorac Surg       Date:  2017-11

6.  Adhesions as a cause of persistent spontaneous pneumothorax.

Authors:  E L Hoover; H K Hsu; K Mkandawire; E Minnard
Journal:  J Natl Med Assoc       Date:  1989-04       Impact factor: 1.798

7.  Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: outflow tract obstruction, coarctation of the aorta, tetralogy of Fallot, Ebstein anomaly and Marfan's syndrome.

Authors:  Candice K Silversides; Marla Kiess; Luc Beauchesne; Timothy Bradley; Michael Connelly; Koichiro Niwa; Barbara Mulder; Gary Webb; Jack Colman; Judith Therrien
Journal:  Can J Cardiol       Date:  2010-03       Impact factor: 5.223

8.  Dural ectasia is a common feature of the Marfan syndrome.

Authors:  R E Pyeritz; E K Fishman; B A Bernhardt; S S Siegelman
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

9.  Marfan syndrome with pneumothorax: case report and review of literatures.

Authors:  Weiming Hao; Yong Fang; Hao Lai; Yaxing Shen; Hao Wang; Miao Lin; Lijie Tan
Journal:  J Thorac Dis       Date:  2017-12       Impact factor: 2.895

10.  High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders.

Authors:  J Pablo Abonia; Ting Wen; Emily M Stucke; Tommie Grotjan; Molly S Griffith; Katherine A Kemme; Margaret H Collins; Philip E Putnam; James P Franciosi; Karl F von Tiehl; Brad T Tinkle; Keith A Marsolo; Lisa J Martin; Stephanie M Ware; Marc E Rothenberg
Journal:  J Allergy Clin Immunol       Date:  2013-04-19       Impact factor: 10.793

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.