Hobbs J R, Corbett A A
Br Med J. 1969 Feb 15;1(5641):412-4. doi: 10.1136/bmj.1.5641.412.
A study of 14 personal patients and 16 others in the literature shows that (1) IgD myelomatosis often presents at a significantly younger age than other forms of myelomatosis, and (2) during life extraosseous tumour can be detected in about two-thirds of these patients.The IgD form represents 1.5% of myelomatosis and shows an increased incidence of osteolytic lesions, hypercalcaemia, and renal failure, together with heavy Bence Jones proteinuria (90% type L).Like only Bence Jones myelomatosis, the IgD form seems to behave clinically in a more vicious manner.
一项针对14例自身患者及文献中另外16例患者的研究表明:(1) IgD型骨髓瘤往往比其他类型的骨髓瘤发病年龄显著更小;(2) 在这些患者中,约三分之二在生前可检测到骨外肿瘤。IgD型占骨髓瘤的1.5%,溶骨性病变、高钙血症和肾衰竭的发生率增加,同时伴有大量本-周蛋白尿(90%为L型)。与仅本-周蛋白型骨髓瘤一样,IgD型在临床上似乎表现得更为凶险。