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A Case of Cardiac Dysfunction Associated with Monoclonal Gammopathy of Undetermined Significance

机译:一例意义不明的伴有单克隆丙种球蛋白病的心功能不全一例

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摘要

The monoclonal gammopathies (MG) are monoclonal neoplasms related to each other by virtue of their development from common progenitors in the B lymphocyte lineage. Cardiac dysfunction in patients with MG is not well established. We experienced a case of cardiac dysfunction associated with MG identified by echocardiography and biopsy. Fifty nine year-old man was admitted because of dyspnea for several months. Echocardiography revealed diastolic dysfunction showing restrictive physiology with elevated left ventricular filling pressure. Bone marrow (BM) studies and immunoelectrophoresis were compatible with monoclonal gammopathy of undetermined significance. Endomyocardial, BM, and enteral biopsies for ruling out for amyloidosis (Congo-red stain) were negative. This is the case of non-amyloidotic light chain deposition cardiomyopathy.
机译:由于它们是从B淋巴细胞谱系中的常见祖细胞发育而来的,因此,它们是彼此相关的单克隆肿瘤。 MG患者的心脏功能障碍尚不明确。我们经历了一例通过超声心动图和活检确定的与MG相关的心脏功能障碍。五十九岁的男子因呼吸困难入院数月。超声心动图显示舒张功能障碍,显示限制性生理,左心室充盈压升高。骨髓(BM)研究和免疫电泳与具有不确定性的单克隆丙种球蛋白病兼容。排除淀粉样变性(刚果红染色)的心肌内膜,BM和肠内活检阴性。非淀粉样蛋白轻链沉积性心肌病就是这种情况。

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