Desai P, Perino G, Present D, Steiner G C
Department of Pathology and Laboratory Medicine, Hospital for Joint Diseases Orthopaedic Institute, New York 10003, USA.
Arch Pathol Lab Med. 1996 May;120(5):482-9.
Sarcoma associated with bone infarct is rare, and only 41 well-documented cases have been published. We describe five additional patients, three women and two men, aged 39 to 57 years. The tumors involved the femur (three patients), tibia (one patient), and humerus (one patient). In three patients, the infarcts were idiopathic. Radiologic evidence of malignancy was found in all patients, and bone infarcts were suspected in four. Four of the patients had malignant fibrous histiocytoma and one an osteosarcoma. Histologically, bone infarcts were seen in all patients, but in three they were mostly replaced by tumor. Portions of intact infarcts were seen adjacent to the tumor, indicating that they had preceded the development of the sarcoma. No hypercellular or atypical reparative tissue was found in the infarcted bones or in three additional uncomplicated infarcts studied from the same patients. The pathogenesis of sarcoma arising in bone infarct is unknown. The prognosis is poor; four of our five patients died within 2 years.
与骨梗死相关的肉瘤很罕见,仅有41例有充分文献记载的病例被发表。我们描述另外5例患者,3名女性和2名男性,年龄在39至57岁之间。肿瘤累及股骨(3例患者)、胫骨(1例患者)和肱骨(1例患者)。3例患者的梗死为特发性。所有患者均发现恶性肿瘤的放射学证据,4例怀疑有骨梗死。4例患者患有恶性纤维组织细胞瘤,1例患有骨肉瘤。组织学上,所有患者均可见骨梗死,但其中3例大部分被肿瘤取代。在肿瘤旁可见部分完整的梗死灶,表明它们先于肉瘤发生。在梗死骨或从同一患者研究的另外3例无并发症的梗死灶中未发现细胞增多或非典型的修复组织。骨梗死中发生肉瘤的发病机制尚不清楚。预后很差;我们的5例患者中有4例在2年内死亡。