多叶单核细胞型浆细胞性骨髓瘤1例

Sneha Kakoty, Anurag Saha, Torsha Jana, Jyoti Sawhney
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引用次数: 1

摘要

浆细胞性骨髓瘤(PCM)约占恶性肿瘤的1%,占血液系统肿瘤的10-15%。它是一种以浆细胞和单克隆免疫球蛋白或游离轻链(FLCs)异常增殖为特征的恶性疾病。骨髓瘤浆细胞有许多形态变异,包括成熟型、未成熟型、浆母细胞型和多形型。在这里,我们报道了一种罕见的PCM表现,其血清蛋白电泳正常,但血清FLC升高,具有卷曲、多叶和单核细胞增多的形态。这种类型的形态学与侵袭性临床过程和对常规化疗的耐药性有关。此外,血清/尿液电泳中M蛋白的缺失并不排除PCM的诊断,血清FLC测定在这类情况下起着重要作用。
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A Case of Plasma Cell Myeloma with Multilobated and Monocytoid Morphology
Plasma cell myeloma (PCM) accounts for approximately 1% of malignant tumors and 10 to 15% of hematological neoplasms. It is a malignant disease characterized by abnormal proliferation of plasma cells and monoclonal immunoglobulins or free light chains (FLCs). There are many morphological variations of the myeloma plasma cells which include mature, immature, plasmablastic, and pleomorphic types. Here, we report a rare presentation of PCM with normal serum protein electrophoresis but elevated serum FLCs and having convoluted, multilobated, and monocytoid morphology. This type of morphology is related to an aggressive clinical course and resistance to conventional chemotherapy. Moreover, absence of M protein in serum/urine electrophoresis does not rule out the diagnosis of PCM and serum FLC assays plays an important role in this kind of scenarios.
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审稿时长
22 weeks
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