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以骨骼为主要表现的恶性淋巴瘤。

Malignant lymphomas with primary bone manifestation.

作者信息

Vassallo J, Roessner A, Vollmer E, Grundmann E

出版信息

Pathol Res Pract. 1987 Jun;182(3):381-9. doi: 10.1016/S0344-0338(87)80074-2.

DOI:10.1016/S0344-0338(87)80074-2
PMID:3628096
Abstract

18 malignant lymphomas with initial manifestation in bone were selected from the Bone Tumor Registry of Westfalia at the Münster Institute of Pathology where they had been documented between 1975 and 1985, and evaluated under clinical, radiological and histological aspects. Non-Hodgkin lymphomas were reclassified according to the Kiel nomenclature. Paraffin-embedded material was subjected to immunohistochemical analysis in order to assess the features that could add to the correct characterization of these lymphomas, and to their differentiation from other round cell tumors of bone. Non-Hodgkin lymphomas (NHL) were more common in the collective than Hodgkin's lymphomas (HL). Of 13 NHL, 2 were of low, 11 of high-grade malignancy. The former comprised one centrocytic and one centroblastic/centrocytic, the latter 7 centroblastic, 2 immunoblastic, and 2 lymphoblastic lymphomas. Seven NHL patients with localized tumors survived up to 11 years (mean survival span: 6 yrs) after local therapy (radiation and/or resection). Another NHL patient, however, had multiple bone lesions, and died within a year. Analysis for leukocyte common antigen was positive in 9/12 NHL cases, reaction with Ki-B-3, a marker of B-lymphocytes, was positive in 7/12 cases. No lymphoma cells were found to react positively with lysozyme, alpha 1-antitrypsin, or alpha 1-antichymotrypsin. It is concluded that localized lymphomas of bone respond well to appropriate local therapy; immunohistochemical investigation may be useful to characterize the true cellular origin of these tumors, and may help to differentiate them from other round cell tumors of bone.

摘要

从明斯特病理研究所威斯特法伦骨肿瘤登记处选取了18例首发于骨骼的恶性淋巴瘤,这些病例于1975年至1985年间有记录,并从临床、放射学和组织学方面进行评估。非霍奇金淋巴瘤根据基尔命名法重新分类。对石蜡包埋材料进行免疫组织化学分析,以评估有助于正确表征这些淋巴瘤以及将它们与其他骨圆形细胞瘤相鉴别的特征。非霍奇金淋巴瘤(NHL)在该组病例中比霍奇金淋巴瘤(HL)更常见。在13例NHL中,2例为低级别恶性,11例为高级别恶性。前者包括1例中心细胞性和1例中心母细胞/中心细胞性淋巴瘤,后者包括7例中心母细胞性、2例免疫母细胞性和2例淋巴母细胞性淋巴瘤。7例局限性肿瘤的NHL患者在局部治疗(放疗和/或手术切除)后存活长达11年(平均生存期:6年)。然而,另1例NHL患者有多处骨病变,在1年内死亡。12例NHL病例中9例白细胞共同抗原分析呈阳性,12例病例中7例与B淋巴细胞标志物Ki-B-3反应呈阳性。未发现淋巴瘤细胞与溶菌酶、α1-抗胰蛋白酶或α1-抗糜蛋白酶呈阳性反应。结论是,局限性骨淋巴瘤对适当的局部治疗反应良好;免疫组织化学研究可能有助于表征这些肿瘤的真正细胞起源,并有助于将它们与其他骨圆形细胞瘤相鉴别。

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Pathol Res Pract. 1987 Jun;182(3):381-9. doi: 10.1016/S0344-0338(87)80074-2.
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