Grabellus Florian, Sheu Sien-Yi, Schmidt Boris, Flasshove Michael, Kuhnen Cornelius, Ruchholtz Steffen, Taeger Georg, Schmid Kurt Werner
Institute of Pathology, University Hospital of Essen, University Duisburg-Essen, Hufelandstrasse 55, 45122 Essen, Germany.
Virchows Arch. 2006 Jan;448(1):85-9. doi: 10.1007/s00428-005-0094-0. Epub 2005 Oct 14.
Leiomyosarcomas (LM) of the soft tissue comprise approximately 5-10% of all soft tissue sarcomas. Besides the classic LM, several distinctly uncommon features of the cellular and growth patterns of LM have been described. The term "dedifferentiated LM" has rarely been used in the literature to describe soft tissue LM containing areas of undifferentiated, pleomorphic appearance or detectable heterologous differentiation. We report on a case of high-grade LM with almost entire transition to an osteosarcoma, which was classified as recurrent high-grade LM with heterologous osteosarcomatous differentiation. The identification of areas with osteosarcomatous dedifferentiation in soft tissue sarcomas can be of clinical importance because of a possible change in oncologic treatment strategies.
软组织平滑肌肉瘤(LM)约占所有软组织肉瘤的5%-10%。除了经典的LM外,还描述了LM细胞和生长模式的一些明显不常见特征。“去分化型LM”这一术语在文献中很少用于描述含有未分化、多形性外观区域或可检测到异源性分化的软组织LM。我们报告了一例高级别LM几乎完全转变为骨肉瘤的病例,该病例被分类为复发性高级别LM伴异源性骨肉瘤分化。软组织肉瘤中骨肉瘤去分化区域的识别可能具有临床重要性,因为这可能会改变肿瘤治疗策略。