Abdalla Iman A, Tabbara Imad A
Bone Marrow Transplant Program, George Washington University Medical Center, Washington, DC 20037, USA.
South Med J. 2002 Jul;95(7):761-4.
Nonsecretory multiple myeloma (NSMM) is a rare variant of the classic form of multiple myeloma (MM) and accounts for 1% to 5% of all cases of MM. The clinical presentation and radiographic findings of NSMM and MM are the same. The diagnosis of MM requires the detection of a monoclonal gammopathy in the serum or urine. In NSMM, however, no such gammopathy can be demonstrated, making the diagnosis more difficult. We describe a 43-year-old African American woman who initially had back pain and pathologic vertebral compression fractures that were thought to be due to osteoporosis. Five months later, hypercalcemia developed and NSMM was diagnosed. No monoclonal gammopathy was found in the serum or urine, but skeletal survey showed diffuse osteolytic lesions, and bone marrow biopsy revealed marked plasmacytosis. The immunohistochemical techniques and chromosomal analysis methods that are currently available are discussed.
非分泌型多发性骨髓瘤(NSMM)是经典型多发性骨髓瘤(MM)的一种罕见变异型,占所有MM病例的1%至5%。NSMM和MM的临床表现及影像学表现相同。MM的诊断需要在血清或尿液中检测到单克隆丙种球蛋白病。然而,在NSMM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43岁的非裔美国女性,她最初有背痛和病理性椎体压缩骨折,最初被认为是由骨质疏松症引起的。五个月后,出现高钙血症,被诊断为NSMM。血清或尿液中未发现单克隆丙种球蛋白病,但骨骼检查显示弥漫性溶骨性病变,骨髓活检显示明显的浆细胞增多。本文讨论了目前可用的免疫组织化学技术和染色体分析方法。