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a Clinic for Cardiovascular Surgery, German Heart Center Munich at the Technical University Munich, Lazarettstrasse 36, Munich, 80636 Germany
b Department of Pediatric Cardiology and Congenital Heart Disease, German Heart Center Munich at the Technical University Munich, Lazarettstrasse 36, Munich, 80636 Germany
c Department of Pathology, Technical University Munich, Ismaningerstrasse 22, Munich, 81675 Germany
d Clinic for Cardiovascular Surgery, German Heart Center Munich at the Technical University Munich, Lazarettstrasse 36, Munich, 80636 Germany
(Email: schreiber{at}dhm.mhn.de; eicken{at}dhm.mhn.de; stefan.seidl{at}lrz.tu-muenchen.de; lange{at}dhm.mhn.de).
Stimulated by the recently published results on mid-term clinical results of a tissue-engineered heart valve [1], we equally began to use the graft. However, we wish to report on a 20-year-old patient who needed an early reoperation. Primarily, a 30-mm, tissue-engineered heart valve was implanted. The patient had previous Fallot repair. At discharge, no gradient was measured across the right ventricular outflow tract. Already, after 6 months, the noninvasive peak systolic Doppler gradient measured 50 mm Hg across the prosthesis. Upon catheterization after 8 months the gradient was 57 mm Hg. The right ventricular end-diastolic volume, which had initially fallen to 120 mL/m2, was then at 188 mL/m2. At the site of the graft, a distinct stenosis was confirmed. Ten months after the initial operation, the tissue-engineered heart valve had to be replaced with a homograft. Macroscopic evaluation showed a narrowing throughout the conduit (Fig 1). A cross section taken at the valvular level histologically showed a lympho-histiocytic infiltrate with focal foreign-body reaction with giant cells and massive pseudo-intimal proliferation. Also, the valves were involved with focal infiltration of lymphocytes, histiocytes, and granulocytes (Fig 1).
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