Kyriakos Michael, El-Khoury Georges Y, McDonald Douglas J, Buckwalter Joseph A, Sundaram Murali, DeYoung Barry, O'Brien Michael P
Division of Surgical Pathology, Campus Box 8118, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Skeletal Radiol. 2007 Mar;36(3):237-47. doi: 10.1007/s00256-006-0113-5. Epub 2006 Apr 25.
Two adult patients are described with multifocal osteolytic lesions radiologically simulating a vascular tumor. One patient had multiple bones involved. Histologically, the individual lesions had the features of the nidus of osteoid osteoma/osteoblastoma. A review of the English language medical literature yielded only one other reported case with similar features. The process is designated as osteoblastomatosis to indicate its bone-forming character, prominent osteoblast proliferation, and multiplicity. The cases are distinguished from multifocal/multicentric osteoid osteoma and osteoblastoma, and from benign and malignant vascular tumors.
描述了两名成年患者,其多灶性溶骨性病变在放射学上模拟血管肿瘤。一名患者有多根骨骼受累。组织学上,单个病变具有骨样骨瘤/骨母细胞瘤巢的特征。对英文医学文献的回顾仅发现另外一例具有类似特征的报道病例。该病变过程被命名为骨母细胞瘤病,以表明其成骨特性、显著的成骨细胞增殖和多发性。这些病例与多灶性/多中心性骨样骨瘤和骨母细胞瘤以及良性和恶性血管肿瘤相鉴别。