Allwood Richard P, Bonacci Emma L, McKinnon Erin
Cardiology Department St Vincent's Hospital Melbourne 41 Victoria Parade Fitzroy 3065 Australia.
Australas J Ultrasound Med. 2020 Dec 20;24(2):106-111. doi: 10.1002/ajum.12238. eCollection 2021 May.
Mitral annular calcification (MAC) is considered a chronic and degenerative process involving the fibrous annulus of the mitral valve. The prevalence of MAC has been reported between 8% and 15%. It significantly increases with age, often seen in females, individuals with hypertension, chronic kidney disease and those with multiple cardiovascular risk factors. Caseous calcification of the mitral annulus (CCMA) (also known as caseoma) is a rare variant of MAC and should be considered in the differential diagnosis with other cardiac masses of the mitral valve. An 85-year-old female presented for a transthoracic echocardiogram with a history of hypertension and a systolic murmur. The echocardiogram demonstrated a possible rare variant of MAC, with independent mobile echodensities identified. Further testing using transoesophageal echocardiography was used to confirm diagnosis and ensure appropriate clinical management was arranged. This case demonstrated CCMA, a benign condition that can be mistaken for cardiac tumours, thrombus, vegetations or abscesses. A low prevalence has been reported between 0.06% and 0.07% and 0.6% of patients with MAC using echocardiography. Echocardiography can provide the initial diagnosis for identification and characterisation of MAC. CCMA appears as a calcified mass with an echolucent, liquid-like inner part, located on the posterior mitral valve annulus. Acoustic shadowing is usually absent. Multi-modality imaging can lead to an accurate diagnosis of CCMA without unnecessary interventions. Transoesophageal echocardiography provides further information on the site and composition of the internal material. Computed tomography (CT) and cardiac magnetic resonance imaging (MRI) can also be used, to confirm the diagnosis and to exclude other differential diagnoses.
二尖瓣环钙化(MAC)被认为是一种涉及二尖瓣纤维环的慢性退行性过程。MAC的患病率据报道在8%至15%之间。其患病率随年龄显著增加,常见于女性、高血压患者、慢性肾病患者以及具有多种心血管危险因素的人群。二尖瓣环干酪样钙化(CCMA)(也称为干酪瘤)是MAC的一种罕见变体,在与二尖瓣的其他心脏肿物进行鉴别诊断时应予以考虑。一名85岁女性因高血压病史和收缩期杂音接受经胸超声心动图检查。超声心动图显示可能为MAC的罕见变体,发现了独立的可移动回声密度。使用经食管超声心动图进行进一步检查以确诊,并确保安排适当的临床管理。该病例显示为CCMA,这是一种可能被误诊为心脏肿瘤、血栓、赘生物或脓肿的良性疾病。据报道,使用超声心动图,CCMA在MAC患者中的患病率较低,为0.06%至0.07%和0.6%。超声心动图可为MAC的识别和特征描述提供初步诊断。CCMA表现为位于二尖瓣后环上的钙化肿物,内部为无回声、液体样部分。通常无声学阴影。多模态成像可在无需不必要干预的情况下准确诊断CCMA。经食管超声心动图可提供有关内部物质部位和成分的进一步信息。计算机断层扫描(CT)和心脏磁共振成像(MRI)也可用于确诊并排除其他鉴别诊断。