Stewart John M M, Krishnamurthy Savitri
Department of Pathology, MD Anderson Cancer Center, University of Texas, Houston, Texas 77030-4095, USA.
Diagn Cytopathol. 2002 Oct;27(4):218-22. doi: 10.1002/dc.10174.
Plasma cell neoplasia occurs much less frequently than high-grade B-cell non-Hodgkins lymphoma in HIV-infected patients, but is nevertheless an AIDS-associated malignancy. In this report, we describe the fine-needle aspiration (FNA) findings of a mass in the left parotid region with plasmablastic features that occurred in a 41-yr-old HIV-infected homosexual man whom we diagnosed as having anaplastic myeloma. The patient had normochromic, normocytic anemia with a hematocrit of 21%, a white blood count of 2.2 x 10(9)/l with 76% neutrophils, and a CD4 count of 31%. He also had elevated levels of calcium (13.2 mg/dl), alkaline phosphatase (25,400 IU/l), blood urea nitrogen (2,600 mg/dl), and creatinine (2.5 mg/dl). Serum protein electrophoresis showed polyclonal hypergammaglobulinemia without any monoclonal component. A bone survey revealed multiple punched-out lytic lesions. FNA smears showed large plasmacytoid cells with eccentrically placed nuclei, prominent nucleoli, and moderate amounts of basophilic cytoplasm. By immunocytochemical staining, tumor cells were negative for CD19, CD20, and leukocyte-common antigen (LCA), but strongly positive for CD38 and kappa light chain. Anaplastic myeloma and plasmablastic lymphoma were considered in the differential diagnosis. Although the cytomorphologic and immunophenotypic findings of our case overlapped with those of plasmablastic lymphoma, the pattern of bone involvement with punched-out lytic lesions and absence of localization of the tumor to the mucosa of the oral cavity led us to a diagnosis of anaplastic myeloma. The patient initially received antiretroviral therapy followed by thalidomide and pulse dexamethasome therapy, but his response was poor. His HIV load increased, and his malignancy rapidly progressed with the development of multiple vertebral lesions, extraosseous extension, and eventually cord compression. He died of the disease less than 2 mo after presentation.
浆细胞肿瘤在HIV感染患者中的发生率远低于高级别B细胞非霍奇金淋巴瘤,但仍是一种与艾滋病相关的恶性肿瘤。在本报告中,我们描述了一名41岁HIV感染的同性恋男性左侧腮腺区具有浆母细胞特征的肿块的细针穿刺(FNA)结果,我们诊断其患有间变性骨髓瘤。该患者为正色素正细胞性贫血,血细胞比容为21%,白细胞计数为2.2×10⁹/L,中性粒细胞占76%,CD4计数为31%。他还存在钙水平升高(13.2mg/dl)、碱性磷酸酶升高(25400IU/L)、血尿素氮升高(2600mg/dl)和肌酐升高(2.5mg/dl)。血清蛋白电泳显示多克隆高球蛋白血症,无任何单克隆成分。骨骼检查发现多个穿凿样溶骨性病变。FNA涂片显示大的浆细胞样细胞,核偏位,核仁突出,有中等量嗜碱性细胞质。通过免疫细胞化学染色,肿瘤细胞CD19、CD20和白细胞共同抗原(LCA)阴性,但CD38和κ轻链强阳性。鉴别诊断考虑了间变性骨髓瘤和浆母细胞淋巴瘤。尽管我们病例的细胞形态学和免疫表型结果与浆母细胞淋巴瘤有重叠,但骨骼受累表现为穿凿样溶骨性病变且肿瘤未局限于口腔黏膜,这使我们诊断为间变性骨髓瘤。该患者最初接受抗逆转录病毒治疗,随后接受沙利度胺和脉冲地塞米松治疗,但反应不佳。他的HIV载量增加,恶性肿瘤迅速进展,出现多个椎体病变、骨外扩展,最终导致脊髓受压。就诊后不到2个月,他死于该疾病。