{"title":"Left Atrial Pseudotumor Caused By Caseous Calcification of the Mitral Annulus, Case Report with Review of Literature","authors":"Simpal Gill, Frank Chen","doi":"10.7156/V4I4P242","DOIUrl":null,"url":null,"abstract":"Caseous calcification of the mitral annulus (CCMA) is a rare form of periannular calcification, occurring in 0.06% of all echocardiographic studies and in 0.63% of all patients with mitral annular calcification. Here, we report a case of CCMA manifesting as a left atrial mass. The patient is a 78-year-old African American female with multiple co-morbidities, who presented with symptomatic coronary artery disease and chest pain. A pre-operative echocardiogram revealed a mass in the posterior wall of the left atrium, which did not appear to affect the mitral valve or protrude into the left atrial chamber. Intra-operatively, white toothpaste-like material was removed from the mass lesion. Gross examination revealed multiple fragments of grey-white friable caseous material, measuring 3 x 2.5 x 1 cm in aggregate. Bacterial and fungal cultures from this material were both negative. Microscopic examination showed this material to be amorphous, non-viable, basophilic, and acellular, with foci of calcification. These morphological features were diagnostic for CCMA. Review of the literature indicated that CCMA is a very rare benign lesion, presenting as a round, tumor-like mass with central echolucencies on echocardiography. We believe our case report will further raise the awareness of CCMA so that pathologists and radiologists can get familiar with this rare disease to avoid potential misdiagnosis.","PeriodicalId":19338,"journal":{"name":"North American journal of medicine & science","volume":"14 1","pages":"242"},"PeriodicalIF":0.0000,"publicationDate":"2011-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"North American journal of medicine & science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7156/V4I4P242","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Caseous calcification of the mitral annulus (CCMA) is a rare form of periannular calcification, occurring in 0.06% of all echocardiographic studies and in 0.63% of all patients with mitral annular calcification. Here, we report a case of CCMA manifesting as a left atrial mass. The patient is a 78-year-old African American female with multiple co-morbidities, who presented with symptomatic coronary artery disease and chest pain. A pre-operative echocardiogram revealed a mass in the posterior wall of the left atrium, which did not appear to affect the mitral valve or protrude into the left atrial chamber. Intra-operatively, white toothpaste-like material was removed from the mass lesion. Gross examination revealed multiple fragments of grey-white friable caseous material, measuring 3 x 2.5 x 1 cm in aggregate. Bacterial and fungal cultures from this material were both negative. Microscopic examination showed this material to be amorphous, non-viable, basophilic, and acellular, with foci of calcification. These morphological features were diagnostic for CCMA. Review of the literature indicated that CCMA is a very rare benign lesion, presenting as a round, tumor-like mass with central echolucencies on echocardiography. We believe our case report will further raise the awareness of CCMA so that pathologists and radiologists can get familiar with this rare disease to avoid potential misdiagnosis.
二尖瓣环干酪样钙化(CCMA)是一种罕见的环周钙化形式,在所有超声心动图研究中占0.06%,在所有二尖瓣环钙化患者中占0.63%。在这里,我们报告一例CCMA表现为左心房肿块。患者是一名78岁的非裔美国女性,患有多种合并症,表现为症状性冠状动脉疾病和胸痛。术前超声心动图显示左心房后壁有肿块,未见影响二尖瓣或凸出左心房。术中,从肿块病变处取出白色牙膏样物质。大体检查显示多个灰白色易碎的干酪状物质碎片,骨料尺寸为3 x 2.5 x 1厘米。该材料的细菌和真菌培养均为阴性。显微镜检查显示该物质无定形,无活力,嗜碱性,无细胞,有钙化灶。这些形态学特征可用于诊断CCMA。回顾文献表明CCMA是一种非常罕见的良性病变,在超声心动图上表现为圆形肿瘤样肿块,中央回声。我们相信我们的病例报告将进一步提高对CCMA的认识,使病理学家和放射科医生熟悉这种罕见的疾病,避免误诊。