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10.1136/bcr-2013-202223 http://scihub22266oqcxt.onion/10.1136/bcr-2013-202223 C4078528!4078528!24966259     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       BMJ+Case+Rep 2014 ; 2014 (ä): ä Nephropedia Template TP {{tp|p=24966259|t=2014. Extreme dilation of pulmonary artery: a literature review |pdf=|usr=}}{{24966259}} gab.com Text Extreme dilation of pulmonary artery: a literature review JO: BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=24966259 #FOAvip Massive pulmonary dilation is a rare finding. These aneurysms can result from different aetiologies that can be congenital or acquired. We present a case of a 61-year-old Caucasian woman who presented with dyspnoea and cough and was discovered to have a massive pulmonary aneurysm. After eliminating most other possible causes, pulmonary hypertension and congenital pulmonic valve stenosis were deemed likely aetiological factors for our patient. These aneurysms are very rare and should prompt close attention and surveillance when present. It is essential to diagnose these findings in a timely fashion as severe complications such as arterial perforation and fatal haemorrhage may occur if left untreated. We present this case because mechanisms leading to pulmonary artery dilation are poorly understood. Furthermore the clinical symptoms and complications are not commonly known, meriting case presentation. Twit Text FOAVip Extreme dilation of pulmonary artery: a literature review ????BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=24966259 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24966259 #FOAvip English Wikipedia <ref>{{Cite pmid|24966259}}</ref> Extreme dilation of pulmonary artery: a literature review #MMPMID24966259 Shafiq A; Bokhari A; Nahin I; Rabbani B BMJ Case Rep 2014[]; 2014 (ä): ä PMID24966259show ga Massive pulmonary dilation is a rare finding. These aneurysms can result from different aetiologies that can be congenital or acquired. We present a case of a 61-year-old Caucasian woman who presented with dyspnoea and cough and was discovered to have a massive pulmonary aneurysm. After eliminating most other possible causes, pulmonary hypertension and congenital pulmonic valve stenosis were deemed likely aetiological factors for our patient. These aneurysms are very rare and should prompt close attention and surveillance when present. It is essential to diagnose these findings in a timely fashion as severe complications such as arterial perforation and fatal haemorrhage may occur if left untreated. We present this case because mechanisms leading to pulmonary artery dilation are poorly understood. Furthermore the clinical symptoms and complications are not commonly known, meriting case presentation. äExtreme dilation of pulmonary artery: a literature review (epmc).pdf DeepDyve Pubget Overpricing