Cattani M G, Viale G, Santini D, Martinelli G N
Department of Pathological Anatomy and Histology, Maggiore Hospital, Bologna, Italy.
Virchows Arch A Pathol Anat Histopathol. 1992;420(5):459-62. doi: 10.1007/BF01600519.
Malignant rhabdoid tumours (MRTs) are highly aggressive neoplasms which most frequently occur in the kidney of young children. Several cases of primary MRT occurring in extra-renal sites have been reported, particularly in the soft tissues. We report a case of primary MRT of the uterus, a very rare site for this neoplasm, with morphological, immunohistochemical and ultrastructural features corresponding to restrictive morphological criteria for MRT. The possible differential diagnoses were considered.
恶性横纹肌样瘤(MRTs)是侵袭性很强的肿瘤,最常发生于幼儿的肾脏。已有多例原发性MRT发生于肾外部位的报道,尤其是软组织。我们报告1例子宫原发性MRT,这是该肿瘤非常罕见的发病部位,其形态学、免疫组化及超微结构特征符合MRT的严格形态学标准。文中考虑了可能的鉴别诊断。