Segesser L v, Cox J, Gross J, Lerch R, Gabathuler J, Glassey F, Gisselbaek A, Faidutti B
Thorac Cardiovasc Surg. 1986 Dec;34(6):391-4. doi: 10.1055/s-2007-1022181.
Primary leiomyosarcoma of the heart is uncommon and we were able to find only 15 cases reported in the literature. Few of these cases were discovered during life and, as a result, even fewer have been treated surgically. We report a case of a right atrial leiomyosarcoma which was proven pathologically (histologically, immunohistochemically and ultrastructurally) after surgical resection. The clinical presentation, morphological, appearances and outcome are compared with those reported in the literature.
原发性心脏平滑肌肉瘤并不常见,我们在文献中仅能找到15例相关报道。这些病例中很少有在生前被发现的,因此,接受手术治疗的更少。我们报告一例右心房平滑肌肉瘤病例,该病例在手术切除后经病理(组织学、免疫组织化学和超微结构)证实。将该病例的临床表现、形态学表现及结果与文献报道的情况进行了比较。