Sukpanichnant S, Cousar J B, Leelasiri A, Graber S E, Greer J P, Collins R D
Department of Pathology, Vanderbilt University School of Medicine, Nashville, TN 37232.
Hum Pathol. 1994 Mar;25(3):308-18. doi: 10.1016/0046-8177(94)90204-6.
Diagnostic criteria in myeloma have not been completely standardized or tested for accuracy; furthermore, marrow findings of prognostic value have not been clearly identified. We studied 176 patients with myeloma to determine the relative value of marrow differential, tissue sections, and immunohistology singly or in concert in the diagnosis of myeloma and to correlate morphologic features with prognosis. Controls were patients with benign marrow plasmacytosis. Homogeneous nodules of plasma cells at least 1/2 high-power field and/or monotypic aggregates of plasma cells filling at least one interfatty marrow space correctly identified myeloma in 83.5% of cases, with no false positives. The current numerical criteria of marrow plasmacytosis > or = 10% occurred in 17.1% of the controls, and 39.7% of patients with myeloma had less than 10% marrow plasmacytosis at presentation. Myeloma was graded histologically into categories of none/minimal, moderate, and marked dysplasia on the basis of dysplastic features and mitoses; these categories correlated well with clinical outcome, with median length of survival of 32.9, 25.2, and 12.9 months, respectively (overall median length of survival of 123 patients with myeloma, 29.2 months). Packing of marrow by tumor and mitoses measuring at least 5/high-power field regardless of grade also was associated with a poor prognosis (median lengths of survival, 15.2 and 11 months, respectively). Myeloma may be diagnosed in the great majority of cases by demonstrating homogeneous nodules and/or monotypic aggregates of plasma cells in the marrow. Prognostic features were shown to include marked dysplasia, mitoses, packing of marrow by tumor, and clinical stage.
骨髓瘤的诊断标准尚未完全标准化,其准确性也未得到验证;此外,具有预后价值的骨髓检查结果尚未明确。我们研究了176例骨髓瘤患者,以确定骨髓细胞分类计数、组织切片和免疫组织学单独或联合应用在骨髓瘤诊断中的相对价值,并将形态学特征与预后相关联。对照组为良性骨髓浆细胞增多症患者。浆细胞均匀结节至少占1/2高倍视野和/或浆细胞单克隆聚集物至少填充一个脂肪骨髓间隙,在83.5%的病例中可正确诊断骨髓瘤,且无假阳性。目前骨髓浆细胞增多症≥10%的数值标准在17.1%的对照组中出现,39.7%的骨髓瘤患者初诊时骨髓浆细胞增多症低于10%。根据发育异常特征和有丝分裂情况,骨髓瘤在组织学上分为无/轻度、中度和重度发育异常三类;这些分类与临床结果密切相关,中位生存期分别为32.9、25.2和12.9个月(123例骨髓瘤患者的总体中位生存期为29.2个月)。无论分级如何,肿瘤填充骨髓和有丝分裂计数至少5个/高倍视野也与预后不良相关(中位生存期分别为15.2和11个月)。在大多数病例中,通过显示骨髓中浆细胞的均匀结节和/或单克隆聚集物可诊断骨髓瘤。预后特征包括重度发育异常、有丝分裂、肿瘤填充骨髓和临床分期。