Bremer R, Niethard F, Ewerbeck V
Abteilung für Orthopädie im Kindesalter, korrektive und stabilisierend Wirbelsäulenchirurgie, Orthopädische Universitätsklinik, Heidelberg.
Orthopade. 1995 Feb;24(1):24-8.
Osteoid osteoma (ICD: 9191/0) and osteoblastoma (ICD: 9200/0) are closely related entities of osteoblastic-type tumors. Osteoid osteoma is a small benign (lesion 1-2 cm or less) neoplasm that is richly vascularized. Nerve fibers within the tissue surrounding the nidus lead to the characteristic pain. A typical finding is the perifocal osseous reaction around the nidus. Osteoblastoma is a progressively growing lesion of a diameter larger than 2 cm; it is sometimes painful and is characterized by the absence of any reactive perifocal bone formation. For both tumors the treatment is complete surgical excision. If the nidus of the osteoid osteoma is removed, the patient will be free of pain. For the osteoblastoma the treatment depends on the stage and localization of the tumor. Forty-seven patients with osteoid osteoma and 10 patients with osteoblastoma have been treated in Heidelberg since 1980. The radiological investigations and surgical treatment are discussed.
骨样骨瘤(国际疾病分类:9191/0)和成骨细胞瘤(国际疾病分类:9200/0)是成骨细胞型肿瘤中密切相关的实体。骨样骨瘤是一种小型良性(病变1 - 2厘米或更小)且血管丰富的肿瘤。病灶周围组织内的神经纤维导致其特征性疼痛。典型表现是病灶周围的局灶性骨反应。成骨细胞瘤是一种直径大于2厘米的进行性生长病变;它有时会疼痛,其特征是不存在任何反应性局灶性骨形成。对于这两种肿瘤,治疗方法都是完整的手术切除。如果切除骨样骨瘤的病灶,患者将不再疼痛。对于成骨细胞瘤,治疗取决于肿瘤的分期和位置。自1980年以来,海德堡共治疗了47例骨样骨瘤患者和10例成骨细胞瘤患者。本文讨论了相关的放射学检查和手术治疗。