Although the exact embryological mechanism of AMV formation is unclear, it may be caused by an abnormal or incomplete separation of the endocardial cushions.[4] Surgery is usually performed because of severe LVOT obstruction or other cardiac reasons.[1]
There was also a mobile thread-like structure attached to the mitral anterior leaflet at the LVOT and its echogenicity was similar to the mitral valve (MV). The fixation area of this structure showed coherence with the cord or papillary muscle. No other congenital anomalies were detected. Preoperative coronary angiography confirmed patent left anterior descending stent. A surgery was planned for aortic stenosis (AS) and aberrant tissue over the MV. Perioperative transesophageal echocardiography (TEE) was performed under general anesthesia and showed a MV-like structure in the LVOT (Figure 1). An echogenic parachute-like structure was present over the anterior MV with dimensions of 35¥18¥8 mm at the ventricular window. This structure was more prominent at peak systole resulting in turbulence in the LVOT. A transverse aortotomy was performed 2 cm above the level of the aortic valve. Through the aortic root, AMV was seen in the superior of the ventricular aspect of the anterior MV, in the lower part of the left leaflet of the aortic valve, and in the annulus with two tendinous chord lesions (Figure 2). The AMV leaflets were explored through the aortotomy in the LVOT and excised without giving damage to other MV structures. A number 19 mechanical valve was replaced in the aortic position. Post-cardiopulmonary bypass TEE showed that the AMV disappeared and the mitral and prosthetic aortic valve functioned normally. The postoperative period was uneventful. The patient was discharged on fifth day with warfarin treatment. Postoperative TTE was normal.
Figure 1: Transesophageal echocardiographic view of the accessory mitral valve.
Figure 2: Perioperative accessory mitral valve tissue image through the aortotomy incision.
As seen in this case, congenital AMV can remain asymptomatic for many years. The literature reports symptoms including dyspnea, syncope, chest pain, palpitations and arrhythmias, cerebrovascular accidents, low cardiac output due to subaortic obstruction, and congestive heart failure.[1,2]
In symptomatic patients and patients who were scheduled for cardiac surgery for different pathologies, accessory valve resection is absolutely recommended.[3] For isolated AMV, the current approach is intervention in patients with significant LVOT gradient (mean gradient of ≥25 mmHg). Patients with LVOT mean gradient under 25 mmHg, are recommended to be followed-up at regular intervals.[1,2]
Although TTE is sufficient for diagnosis, perioperative TEE is helpful for both confirmation of the diagnosis and evaluation of the MV functions after excision.[5,6] Transesophageal echocardiography is also important in the evaluation of possible complications that may occur after excision and revision of cardiopulmonary bypass for repair and completion of the surgical procedure.
Despite limited experience in the fields of AMV, and frequency of surgical treatment, and methodology in the literature, it is stated that AMV excision could be performed via right or left atriotomy.[
1) Manganaro R, Zito C, Khandheria BK, Cusmà-Piccione M,
Chiara Todaro M, Oreto G, et al. Accessory mitral valve
tissue: an updated review of the literature. Eur Heart J
Cardiovasc Imaging 2014;15:489-97.
2) Rovner A, Thanigaraj S, Perez JE. Accessory mitral valve in
an adult population: the role of echocardiography in diagnosis
and management. J Am Soc Echocardiogr 2005;18:494-8.
3) Prifti E, Bonacchi M, Bartolozzi F, Frati G, Leacche M,
Vanini V. Postoperative outcome in patients with accessory
mitral valve tissue. Med Sci Monit 2003;9:RA126-33.
4) Cremer H, Bechtelsheimer H, Helpap B. Forms and
development of subvalvular aortic stenosis. Virchows Arch
A Pathol Pathol Anat 1972;355:123-34. [Abstract]