Puri Arun, Wadhwa Heena, Singh Navtej
Baba Farid University of Health Sciences, Faridkot, India.
Iran J Pathol. 2018 Spring;13(2):281-284. Epub 2018 Jul 17.
Multiple Myeloma is a neoplasm of B cell lineage characterized by excessive proliferation of abnormal plasma cells. It is characterized by a clinical pentad of 1) anemia, 2) a monoclonal protein in the serum or the urine or both, 3) bone leisons and or bone pain, 4) hypercalcemia>11.5g/dl and 5) renal insufficiency. Non secretory multiple myeloma is a rare variant of the classic form of multiple myeloma and accounts for 1% to 5 % of all cases of multiple myeloma. The clinical presentation and radiographic findings of non-secretory multiple myeloma and multiple myeloma are the same. The diagnosis of multiple myeloma requires the demonstration of monoclonal gammopathy in the serum or urine. In non-secretory multiple myeloma, however no such gammopathy can be demonstrated, making the diagnosis more difficult. We describe a 60 year old woman who initially presented with back pain which when further investigated by complete blood count revealed hemoglobin of 13g/dl, Total Leukocyte Count of 10,890 and platelet count of 1.5 lac/cmm. Viral markers revealed HCV positive. Hypercalcemia with a serum calcium level of 12.5g/dl was also demonstrated. MRI revealed multiple lytic bony lesions. No monoclonal gammopathy was found in the serum or urine and bone marrow biopsy showed marked plasmacytosis of > 45%. We present a case of Non Secretory multiple myeloma because of its illusive nature and rare entity.
多发性骨髓瘤是一种B细胞系肿瘤,其特征为异常浆细胞过度增殖。其临床特征包括五联征:1)贫血;2)血清或尿液或两者中存在单克隆蛋白;3)骨病变和/或骨痛;4)高钙血症(血钙>11.5g/dl);5)肾功能不全。非分泌型多发性骨髓瘤是经典型多发性骨髓瘤的一种罕见变体,占所有多发性骨髓瘤病例的1%至5%。非分泌型多发性骨髓瘤和多发性骨髓瘤的临床表现及影像学表现相同。多发性骨髓瘤的诊断需要在血清或尿液中证实存在单克隆丙种球蛋白病。然而,在非分泌型多发性骨髓瘤中,无法证实存在这种丙种球蛋白病,这使得诊断更加困难。我们描述了一名60岁女性,最初表现为背痛,经全血细胞计数进一步检查发现血红蛋白为13g/dl,白细胞总数为10890,血小板计数为15万/立方毫米。病毒标志物显示丙肝病毒阳性。还证实存在血清钙水平为12.5g/dl的高钙血症。磁共振成像显示多处溶骨性骨病变。血清或尿液中未发现单克隆丙种球蛋白病,骨髓活检显示浆细胞显著增多(>45%)。鉴于非分泌型多发性骨髓瘤的隐匿性和罕见性,我们报告了这一病例。