Literature DB >> 24970003

Papillary fibroelastoma of the pulmonary valve: a case report.

Adrian Molnar1, Svetlana Encică, Emese Kovács, Simona Manole, Diana Săcui, Ioan Mureşan, Traian Scridon.   

Abstract

Papillary fibroelastoma is a rare, benign cardiac tumor typically found on the heart valves, which is usually discovered incidentally on echocardiography. The clinical presentation of cardiac papillary fibroelastoma varies from no symptoms to severe embolic sequelae. We report the case of a 55-year-old female patient, with a suspicion of pulmonary embolism one year before, presently admitted to the hospital for mild respiratory symptoms; the trans-esophageal echocardiography (TEE) revealed a 10/10 mm tumoral mass attached on the pulmonary valve, confirmed also by the contrast-enhanced magnetic resonance imaging (MRI). Considering the embolization risk, we decided surgical removal, with favorable outcome. The pathologic exam of the removed tumor established the diagnosis of papillary fibroelastoma. The clinical and imaging assessment one month after surgery were within normal limits. The surgical removal of the papillary fibroelastoma of the pulmonary valve is mandatory for the elimination of embolization risk. The intervention is relatively secure, with low rates of morbidity and mortality.

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Year:  2014        PMID: 24970003

Source DB:  PubMed          Journal:  Rom J Morphol Embryol        ISSN: 1220-0522            Impact factor:   1.033


  2 in total

1.  Surgical treatment of papillary fibroelastoma of the pulmonary valve: a case report.

Authors:  Hiroo Uehara; Masateru Uchiyama; Takayuki Hori; Mitsuru Iida; Tomohiro Imazuru; Tomoki Shimokawa
Journal:  J Cardiothorac Surg       Date:  2022-06-09       Impact factor: 1.522

2.  Papillary fibroelastoma of the aortic valve presenting with chronic angina and acute stroke: a case report.

Authors:  Fan Zhang; Ziqiang Zhu; Gautham K Upadhya; Jiankun Tong; Vlad Gotlieb; Abdullah Khan; Rakesh P Gupta
Journal:  J Med Case Rep       Date:  2017-01-18
  2 in total

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