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混合性骨肿瘤:骨脂肪肉瘤和骨横纹肌肉瘤。

Bone tumors of mixed origin: osteo-liposarcoma and osteo-rhabdomyosarcoma.

作者信息

Marcial-Seoane R A, Marcial-Seoane M A, Dávila-Toro F J, Marcial-Rojas R A

机构信息

Department of Radiology, School of Medicine, Universidad Central del Caribe, Bayamón, Puerto Rico 00621-6032.

出版信息

Bol Asoc Med P R. 1990 Sep;82(9):378-93.

PMID:2076143
Abstract
  1. A complete perusal of the literature revealed twenty cases of primary liposarcoma of bone acceptable as such to the authors. These were tabulated as to location and age. 2. Eight cases of osteo-liposarcoma, primary in bone, were encountered in the literature and an additional case was reported by the authors. 3. The authors described for the first time in the literature a new primary tumor of bone of mixed origin: osteo-rhabdomyosarcoma. After careful perusal of the literature they added three additional cases: two cases, previously reported as primary rhabdomyosarcoma of bone, which on careful evaluation of the radiographs in said publications and the paucity of microphotographs they considered to be osteo-rhabdomyosarcomas, and the other case, previously reported as malignant mesenchymoma of the sternum following radiotherapy for breast cancer. 4. The authors prefer to classify these tumors (osteo-liposarcoma and osteo-rhabdomyosarcoma) as "Tumors of Mixed Origin" and not as "Malignant Mesenchymomas". 5. A complete review of the literature revealed 219 reported "dedifferentiated" chondrosarcomas, or chondrosarcomas "with additional mesenchymal component", among which only nine (9) contained a bona fide rhabdomyosarcomatous component. The rest exhibited other mesenchymal tumors as osteogenic sarcoma, fibrosarcoma, malignant fibrous histiocytoma, angiosarcoma, and undifferentiated sarcoma. The authors recommend to continue classifying these tumors as chondrosarcomas with additional mesenchymal component or even as "dedifferentiated" chondrosarcomas but not as malignant mesenchymomas.
摘要
  1. 全面查阅文献后,作者发现了20例可被认定为原发性骨脂肪肉瘤的病例。这些病例按部位和年龄进行了列表。2. 文献中发现了8例原发性骨骨肉瘤,作者还报告了1例。3. 作者在文献中首次描述了一种新的混合起源的原发性骨肿瘤:骨横纹肌肉瘤。在仔细查阅文献后,他们又补充了3例:2例之前被报告为原发性骨横纹肌肉瘤,经仔细评估上述出版物中的X光片以及微观照片数量稀少后,他们认为这两例应为骨横纹肌肉瘤;另一例之前被报告为乳腺癌放疗后胸骨恶性间叶瘤。4. 作者倾向于将这些肿瘤(骨肉瘤和骨横纹肌肉瘤)归类为“混合起源肿瘤”,而非“恶性间叶瘤”。5. 全面回顾文献发现,有219例报告的“去分化”软骨肉瘤,或“伴有额外间叶成分”的软骨肉瘤,其中只有9例含有真正的横纹肌肉瘤成分。其余病例表现为其他间叶肿瘤,如骨肉瘤、纤维肉瘤、恶性纤维组织细胞瘤、血管肉瘤和未分化肉瘤。作者建议继续将这些肿瘤归类为伴有额外间叶成分的软骨肉瘤,甚至归类为“去分化”软骨肉瘤,而不是恶性间叶瘤。

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