Mycotic pulmonary artery pseudoaneurysm following total arch replacement: a case report

A 68-year-old woman was referred to our department for 2 weeks with fever of unknown origin. She had a history of emergency TAR for an acute type A aortic dissection 4 months earlier and chronic rheumatoid arthritis on monthly subcutaneous tocilizumab treatment for several years. At the initial surgery, the patient presented with paraplegia and urinary tract infection as postoperative complications and was transferred to another facility for rehabilitation.

A blood culture was positive for Enterococcus faecalis. Transthoracic and transesophageal echocardiography revealed a left ventricular ejection fraction of 58%, severe mitral regurgitation with a 15-mm-diameter vegetation on the anterior mitral leaflet, and severe aortic insufficiency with string-like structures. Contrast computed tomography (CT) revealed a focal saccular outpouching from the right pulmonary artery (Fig. 1A). On 18F-fluorodeoxyglucose positron emission tomography (FDG-PET), focal uptake of FDGs was observed along the same lesion of the pulmonary artery and ascending-arch graft (Fig. 1B, C).

Fig. 1figure 1

A Preoperative contrast CT showed a focal saccular outpouching from the right pulmonary artery (red arrowhead). B, C Preoperative FDG-PET showed focal uptake of FDGs along the PAP (red arrowhead) and ascending-arch graft (blue arrowhead)

Infective endocarditis and ascending-arch graft infection, concomitant with mycotic PAP, were strongly suspected. Because of the size of the vegetation and rapid progressive heart failure, urgent surgery was performed. Before re-sternotomy, the femoral artery and vein were taped through a right inguinal incision in preparation for cannulation. Upon re-sternotomy, the pericardial space was dissected. Because of sudden massive bleeding from the dorsal aspect of the ascending aortic graft, while manual control of the bleeding was attempted, a cardiopulmonary bypass with ascending side branch cannulation and bi-caval venous drainage was hastily initiated, and systemic cooling was started simultaneously.

After cross clamping of the ascending aortic graft, the proximal aortic graft was removed and a large defect was found ventral to the right pulmonary artery (Fig. 2A). In addition, disruptions were noted on the dorsal aspect of the proximal suture line. Observation of the mitral valve revealed large vegetation on the anterior mitral leaflet. Both leaflets were removed and replaced with a 27-mm Epic mitral bioprosthesis (Abbott Medical Japan, Co. Ltd, Tokyo, Japan). The aortic valve was also replaced with a 21-mm Edwards Inspiris RESILIA aortic bioprosthesis (Edwards Lifesciences, Irvine, CA, USA). Re-TAR was then performed with a 22-mm 4-branched rifampicin bonded graft (Gelweave Ante-Flo Gelatin Impregnated Woven Dacron Graft, Sulzer Vascutek, Renfrewshire, Scotland) using antegrade cerebral perfusion. Reconstruction of the right pulmonary artery was performed using a bovine pericardial patch (Fig. 2B). Finally, an omental flap was applied to the anterior mediastinum before sternal closure. The operation time was 668 min and the aortic cross clamp time was 231 min. Culture tests performed intraoperatively detected Enterococcus faecalis in the mitral valve, aortic valve, ascending-arch graft, and PAP.

Fig. 2figure 2

A Operative image after aortic graft clamping, removal of ascending aortic graft. A large defect was found ventral to the right pulmonary artery (white dotted line). The blue arrowhead shows the Swan–Ganz catheter in the pulmonary artery. B Operative image after PAP repair using a bovine pericardial patch (white dotted line). C Postoperative 3D-CT revealed favorable reconstruction of the right pulmonary artery

Fever resolved immediately after surgery. Postoperative 3D-CT revealed favorable reconstruction of the right pulmonary artery (Fig. 2C). The patient was discharged after 6 weeks of intravenous double-therapy with antibiotics (CTRX, ABPC/MCIPC), followed by lifelong oral AMPC. Currently, after 1 year, careful monitoring is in progress without any evidence of re-infection.

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