Department of Pathology, Florida Hospital Orlando, Orlando, FL 32803, USA.
Int J Gynecol Pathol. 2012 Sep;31(5):453-7. doi: 10.1097/PGP.0b013e318246977d.
Heterologous differentiation in metastatic leiomyosarcomas of uterine origin is an extremely rare phenomenon. We report a remarkable case of a metastatic leiomyosarcoma from the uterus with an unusual pattern of tumor progression to malignant mesenchymoma after chemotherapy. The patient, an 80-yr-old woman with a history of metastatic leiomyosarcoma of the uterus to the lungs, presented with a large intra-abdominal mass. Histologic examination of the intraperitoneal mass demonstrated a high-grade sarcoma containing various heterologous malignant mesenchymal elements including osteosarcoma, chondrosarcoma, a liposarcoma-like area, and osteoclast-like multinucleated giant cells. Only the identification of small areas of smooth muscle differentiation revealed the true nature of the tumor as a metastatic leiomyosarcoma with aberrant sarcomatous differentiation. This unique presentation emphasizes the importance of clinicopathologic correlation in the diagnosis of tumors with unusual histology.
转移性子宫来源平滑肌肉瘤的异源性分化是一种极为罕见的现象。我们报告了一例转移性子宫平滑肌肉瘤的显著病例,该肿瘤在化疗后出现了恶性间叶瘤样的不常见肿瘤进展模式。该患者为 80 岁女性,有转移性子宫平滑肌肉瘤肺转移病史,表现为巨大的腹腔内肿块。腹腔内肿块的组织学检查显示高级别肉瘤,包含多种异源性恶性间叶成分,包括骨肉瘤、软骨肉瘤、脂肪肉瘤样区域和破骨细胞样多核巨细胞。只有识别出少量平滑肌分化区域,才能揭示肿瘤的真实性质,即转移性平滑肌肉瘤伴异常肉瘤样分化。这种独特的表现强调了在诊断具有不常见组织学表现的肿瘤时临床病理相关性的重要性。