LAUSR

In a 78-year-old woman, with history of mitral valve (MV) calcifications and sepsis by Staphylococcus hominis with brain micro-embolisms, we diagnosed, by non-invasive imaging, the infective rupture of caseous calcification of the mitral annulus (CCMA), with complete ventricular–atrial fistulization. Trans-thoracic echocardiography (Fig. 1) revealed a gross calcification of the medial commissure of the MV in apical 4-chamber view (panel a), which was confirmed in short-axis view, as involving the posterior mitral annulus from the commissure towards P3 and P2 (panel b); slightly tilting the probe upward from the short-axis view, the medial commissure calcification appeared hypoechogenic in the core, as can be seen in caseous necrosis of calcified annulus (panel c). By colorDoppler mode, huge mitral regurgitation (MR) with jet crossing the CCMA from the ventricular to the atrial side could be detected, both in 4-chamber view (panel d) and short-axis view (panel e). Trans-esophageal echocardiography confirmed and better defined the lesion: in mid-esophageal bicommissural view by black and white mode (Video 1, Fig. 2 panel a), the round-shaped calcification of the medial commissure appeared excavated with frayed and fluctuating edges on the atrial side, which could not be appreciated at transthoracic echocardiography due to calcium shadowing. Twoand three-dimensional colorDoppler mode (Videos 2 and 3), also implemented by contemporary visualization of 2 orthogonal planes (Fig. 2 panel b) showed that MR jet entered the lesion from the ventricular side at the basal portion of the MV and came out on the atrial side at 2 sites, one central and one on the posterior side of CCMA, leading to complete ventricular–atrial fistulization. Scanning the entire MV by colorDoppler mode, revealed MR jet spreading also to the centro-lateral portion, as originating along the coaptation rim (Fig. 2 panel c) and definitively leading to judge MR as severe. Classical volume rendering (Video 4, Fig. 2 panel d) of the atrial side of MV showed the extensive calcification of the posterior mitral annulus, and the large calcified mass of the medial mitral commissure extended to A3. At this level, by changing the light in the photo-realistic mode, the 2 sites of rupture, on the posterior side of CCMA (Video 5) and centrally (Video 6), could be alternatively and impressively visualized. Computed tomography (CT) showed multiple splanchnic and cerebral embolization, and a large dense calcified mass involving the posterior and anterior mitral annulus. The CT axial slice, crossing the A3–P3 portion of the MV and showing the mitral annulus calcification, is displayed in panel e. As the patient had been recently hospitalized for multifocal pneumonia and brain micro-embolisms, which were initially judged to origin from thrombosis on the CCMA, and only subsequently peripheral blood cultures suggested Staphylococcus hominis bacteremia, a positron emission tomography with 18F-fluoro-deoxy-glucose (PET) was performed to confirm active infection of CCMA. To minimize physiological FDG myocardial uptake, the patient was asked to observe a very low-carbohydrate, high-protein and high-fat diet the day before PET imaging and then to fast overnight on the day before imaging, while heparin was not administered before examination. Nevertheless, an intense and diffuse myocardial uptake was found, which was conceivably in keeping with the widespread inflammatory and metabolic activation secondary to the septic state. Unfortunately, it prevented adequate evaluation of the mitral annulus uptake, as can be seen in the corresponding axial slice at positron emission tomography (panel f). Because of several concerns about calcification of mitral annulus, the patient was initially denied from cardiac surgery. However, as her * Gabriella Locorotondo [email protected]; [email protected]