Chow Louis T C
Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, Hong Kong, China.
APMIS. 2016 Jun;124(6):487-99. doi: 10.1111/apm.12540. Epub 2016 Apr 22.
In accordance with recent terminology, it is proposed that malignant mesenchymoma should be renamed 'composite sarcoma' and defined as 'a sarcoma composed of two or more cellular types each of which is sufficiently differentiated to permit clear recognition of its histogenetic type microscopically, immunohistochemically or ultrastructurally; excluding fibrosarcomatous and high-grade pleomorphic undifferentiated sarcomatous component, dedifferentiated sarcoma and the combination of osteosarcoma and chondrosarcoma which is regarded as a single histogenetic type'. Four cases of primary osseous composite sarcoma (POCS) were identified among 928 primary bone sarcomas. Their age ranged from 10 to 87 years, peak incidence in the second decade with equal sex distribution. Most presented with pain, commonest in the knee, affecting the metaphysis, appearing radiologically as expansile infiltrative osteolytic lesions with cortical erosion, periosteal reaction, variable extent of osteoblastic areas and soft tissue extension. All contained variable amounts of conventional high-grade osteosarcoma with or without chondrosarcoma component; the other constituents were liposarcoma, rhabdomyosarcoma and leiomyosarcoma. In all cases, Ki67 proliferative index was over 35%, there was no CDK4 and MDM2 amplification. The absence of low-grade component supported the de novo origin of POCS rather than derivation from divergent dedifferentiation. The two older patients with hitherto undescribed osteoleiomyosarcoma died 2 and 10 months after operation, whereas the two younger with osteorhabdomyosarcoma and osteoliposarcoma enjoyed disease-free survival at 16 and 6 years after chemotherapy despite the latter showing lung metastasis at presentation. Identification of the different lines of differentiation together with their approximate amounts and histological grades is therefore mandatory for POCS as multi-agent chemotherapy catered for each sarcoma component might offer hope for long-term disease-free survival.
根据最近的术语,建议将恶性间叶瘤重新命名为“复合肉瘤”,并定义为“由两种或更多细胞类型组成的肉瘤,每种细胞类型都有足够的分化程度,以便在显微镜下、免疫组织化学或超微结构上能够清晰识别其组织发生类型;不包括纤维肉瘤和高级别多形性未分化肉瘤成分、去分化肉瘤以及被视为单一组织发生类型的骨肉瘤和软骨肉瘤的组合”。在928例原发性骨肉瘤中,确诊了4例原发性骨复合肉瘤(POCS)。患者年龄从10岁到87岁不等,发病高峰在第二个十年,男女发病率相等。大多数患者表现为疼痛,最常见于膝关节,累及干骺端,放射学表现为膨胀性浸润性溶骨性病变,伴有皮质侵蚀、骨膜反应、不同程度的成骨区域和软组织延伸。所有病例均含有不同数量的传统高级别骨肉瘤,伴有或不伴有软骨肉瘤成分;其他成分包括脂肪肉瘤、横纹肌肉瘤和平滑肌肉瘤。所有病例中,Ki67增殖指数均超过35%,未发现CDK4和MDM2扩增。缺乏低级别成分支持POCS的原发起源,而非源自不同的去分化。两名患有此前未描述的骨平滑肌肉瘤的老年患者分别在术后2个月和10个月死亡,而两名患有骨横纹肌肉瘤和骨脂肪肉瘤的年轻患者在化疗后分别在16年和6年无病生存,尽管后者在初诊时出现了肺转移。因此,对于POCS来说,确定不同的分化谱系及其大致数量和组织学分级是必不可少的,因为针对每个肉瘤成分的多药化疗可能为长期无病生存带来希望。