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一例侵袭性多发性骨髓瘤,伴有核分裂、多叶状及单核细胞样核,且无血清单克隆丙种球蛋白病。

A case of aggressive multiple myeloma with cleaved, multilobated, and monocytoid nuclei, and no serum monoclonal gammopathy.

作者信息

Yeh Y A, Pappas A A, Flick J T, Butch A W

机构信息

Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, USA.

出版信息

Ann Clin Lab Sci. 2000 Jul;30(3):283-8.

Abstract

Multiple myeloma is a B-cell malignancy characterized by proliferation of neoplastic plasma cells. A few cases have been reported identifying variant forms of neoplastic plasma cells with atypical nuclei that secrete myeloma protein. We report a highly unusual case of plasma cell myeloma that presented with cleaved, multilobated, and monocytoid nuclei, without detectable myeloma protein in the serum or urine. The bone marrow contained sheets of plasma cells exhibiting pleomorphic nuclei with cleaved, multilobated, and monocytoid features that were negative for myeloperoxidase and dual esterase. Flow cytometric analysis revealed CD38high/CD45low cells expressing cytoplasmic kappa light chain, without evidence of myeloid or lymphoid differentiation. Following chemotherapy, the patient developed secondary plasma cell leukemia. A high plasma cell labeling index was obtained from bone marrow and peripheral blood, indicating a poor prognosis. In addition to quantitative immunoglobulins, serum protein electrophoresis, and immunofixation electrophoresis of serum and urine, we recommend cytochemical and flow cytometric studies for evaluation of suspected plasma cell myeloma with atypical cellular features.

摘要

多发性骨髓瘤是一种以肿瘤性浆细胞增殖为特征的B细胞恶性肿瘤。已有少数病例报道发现具有非典型核的肿瘤性浆细胞变异形式,这些细胞可分泌骨髓瘤蛋白。我们报告了一例非常罕见的浆细胞骨髓瘤病例,其肿瘤性浆细胞具有核分裂、多叶状和单核样形态,血清和尿液中未检测到骨髓瘤蛋白。骨髓中可见成片的浆细胞,其核呈多形性,具有核分裂、多叶状和单核样特征,髓过氧化物酶和双酯酶染色阴性。流式细胞术分析显示CD38高/CD45低的细胞表达胞质κ轻链,无髓系或淋巴系分化证据。化疗后,患者发展为继发性浆细胞白血病。骨髓和外周血的浆细胞标记指数较高,提示预后不良。除了定量免疫球蛋白、血清蛋白电泳以及血清和尿液的免疫固定电泳外,我们建议对疑似具有非典型细胞特征的浆细胞骨髓瘤进行细胞化学和流式细胞术研究以进行评估。

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