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镰状细胞贫血患者出现骨化软组织平滑肌瘤
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作者 lacouture m. Petronic-Rosic V. +1 位作者 C.R. Shea 沈斌 《世界核心医学期刊文摘(皮肤病学分册)》 2006年第5期11-11,共1页
Osseous metaplasia in leiomyomas is extremely rare. Here, we report the case of an ossified subcutaneous leiomyoma in a 34-year-old African American man with sickle cell thalassemia who presented with a painful nodule... Osseous metaplasia in leiomyomas is extremely rare. Here, we report the case of an ossified subcutaneous leiomyoma in a 34-year-old African American man with sickle cell thalassemia who presented with a painful nodule of the scapular region, which appeared as a heavily mineralized soft tissue mass on chest radiographs. Histopathologic and immunohistochemical examination of the resected nodule revealed a benign soft tissue leiomyoma composed of intersecting fascicles of spindle cells that strongly expressed smooth muscle actin and caldesmon. Extensive intratumoral calcification and ossification were noticed. Only eight cases of ossified leiomyoma have been reported, of which two arose in the deep soft tissue. Those cases are briefly reviewed and discussed. 展开更多
关键词 平滑肌瘤 镰状细胞贫血 地中海贫血 钙调结合蛋白 梭形细胞 痛性结节 平滑肌肌动蛋白 深部软组织
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