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骨母细胞瘤:16例患者的分类及报告

Osteoblastoma: classification and report of 16 patients.

作者信息

Tonai M, Campbell C J, Ahn G H, Schiller A L, Mankin H J

出版信息

Clin Orthop Relat Res. 1982 Jul(167):222-35.

PMID:7094467
Abstract

In 16 patients who had osteoblastoma treated within the last eight years, the lesions can be classified as vertebral (four cases), central "benign" (seven cases), "aggressive" (three cases) and periosteal (two cases). The radiographic features were highly variable except for the consistent shell of reactive periosteal bone. None of the lesions resembled osteoid osteoma or osteosarcoma. The histological pattern was typical, showing sheets of osteoblasts forming irregular, poorly ossified bone trabeculae in a fibrovascular stroma. The three "aggressive" lesions had a distinctly more ominous histologic pattern, a more destructive radiographic appearance and recurred promptly following local curettage. Treatment varied, but for the vertebral, benign "central," and periosteal osteoblastomas, curettage or marginal resection was generally curative. Local wide resection was required for individual aggressively growing tumors.

摘要

在过去八年中接受治疗的16例骨母细胞瘤患者中,病变可分为椎体型(4例)、中央“良性”型(7例)、“侵袭性”型(3例)和骨膜型(2例)。除了反应性骨膜骨形成的连续骨壳外,影像学特征变化很大。没有病变类似于骨样骨瘤或骨肉瘤。组织学模式典型,显示成骨细胞片层在纤维血管基质中形成不规则、骨化不良的骨小梁。三个“侵袭性”病变具有明显更不祥的组织学模式、更具破坏性的影像学表现,并且在局部刮除后迅速复发。治疗方法各不相同,但对于椎体、良性“中央”和骨膜型骨母细胞瘤,刮除或边缘切除通常可治愈。个别侵袭性生长的肿瘤需要进行局部广泛切除。

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