Larsson S E, Lorentzon R, Boquist L
J Bone Joint Surg Am. 1975 Jan;57(1):84-9.
The clinical and histopathological characteristics are described in seven cases of malignant hemangioendothelioma of bone. This rare neoplasm affects all age groups and almost any bone. Metastases appear in the skeleton even before such lesions are seen on pulmonary roentgenograms. Prognosis is poor, with a five-year survival for only two of the six patients in this series. One patient is still alive and free of symptoms more than twelve years after diagnosis of widespread tumor destruction of the frontal skull bones, which was successfully controlled by radiation therapy. In addition, a recently diagnosed case of this tumor arising in a chronic non-fistulous osteomyelitic bone is described.
本文描述了7例骨恶性血管内皮瘤的临床和组织病理学特征。这种罕见的肿瘤可发生于所有年龄组，几乎累及任何骨骼。甚至在肺部X线片上出现病变之前，转移就已出现在骨骼中。预后较差，该系列6例患者中只有2例存活了5年。1例患者在诊断为额骨广泛肿瘤破坏后12年多仍存活且无症状，该肿瘤通过放射治疗得到成功控制。此外，还描述了1例最近诊断出的发生在慢性非瘘管性骨髓炎骨中的该肿瘤病例。
