01 February 2006
Dyspnea in a patient with aortic aneurysm history: initial manifestation of Takayasu arteritis
Lampros Raptis , Georgios Pappas , Georgios Passas , Konstantinos Bugias , Violeta Maltabe , Nikolaos AkritidisCase Rep Clin Pract Rev 2006; 7:170-173 :: ID: 452943
Abstract
Background: Pulmonary arteries’ involvement is well described in Takayasu’s arteritis, a condition that is
mainly associated with involvement of the systemic arteries.
Case Report: The purpose of this article is to report a case of a 73-year-old woman, who presented with
increasing exertional dyspnea, caused by pulmonary artery involvement in Takayasu’s arteritis,as shown by narrowing of the right pulmonary artery in digital angiography. The diagnosis was set by clinical and angiographic findings as proposed by The American College of Rheumatology(ACR). The patient was treated with immunosuppressive therapy with improvement in both diagnostic imaging and laboratory findings. The patient reported a history of aortic aneurysm in her youth, probably associated with Takayasu arteritis, but the latter remained unrecognised until pulmonary involvement became symptomatic.
Conclusions: In literature review, only a few cases of Takayasu disease have been reported with dyspnea as
initial manifestation. Awareness of this unusual presentation may augment in rapid orientation
of differential diagnosis and proper early treatment.
Keywords: Dyspnea, Pulmonary Artery, Takayasu, Vasculitis
969
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.953733
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.952819
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.952834
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.953320
Most Viewed Current Articles
07 Dec 2021 : Case report
22,763,442
DOI :10.12659/AJCR.934347
Am J Case Rep 2021; 22:e934347
06 Dec 2021 : Case report
177,632
DOI :10.12659/AJCR.934406
Am J Case Rep 2021; 22:e934406
21 Jun 2024 : Case report
121,433
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
66,540
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133






