WOLMAN L
J Clin Pathol. 1961 Mar;14(2):109-14. doi: 10.1136/jcp.14.2.109.
A case is reported in which the amputation of a leg for a sclerosing type of osteogenic sarcoma was followed five years later by a metastasis of similar appearance in the skull. This was excised but subsequent necropsy revealed multiple bony tumours in the lungs. The rarity of multiple osteogenic sarcoma is recalled as shown by a review of the literature. Although some are thought to be of multicentric origin owing to the short history, an early haematogenous spread cannot be excluded and this latter process had certainly occurred in the present case. The characteristic radiological appearances in the skull are stressed as being diagnostic. The differential points in the histological diagnosis of the condition, especially in the invaded part of the calvarium, are described and should help to exclude a meningioma or other bone tumours.
报告了一例因硬化型骨肉瘤行截肢术的病例,五年后颅骨出现了外观相似的转移灶。该转移灶被切除,但随后的尸检显示肺部有多个骨肿瘤。通过文献回顾表明,多发性骨肉瘤很罕见。尽管有些病例由于病程短被认为是多中心起源,但不能排除早期血行转移,本病例肯定发生了后者这种情况。强调了颅骨典型的放射学表现具有诊断价值。描述了该病组织学诊断中的鉴别要点,特别是在颅骨受侵部位,这有助于排除脑膜瘤或其他骨肿瘤。