Ostuni P, Vertolli U, Marson P
Division of Rheumatology, University of Padova, Italy.
Clin Rheumatol. 1996 Nov;15(6):610-2. doi: 10.1007/BF02238553.
A case of hypergammaglobulinaemia D and periodic fever syndrome, developing an amyloidosis-related nephrotic syndrome, is reported. Since such a complication represents a typical feature of another disease characterized by recurrent febrile attacks, i.e., familial Mediterranean fever, an overlap syndrome between these two rare clinical disorders can be suggested.
报告了一例高丙种球蛋白血症D和周期性发热综合征患者,其发展为淀粉样变性相关的肾病综合征。由于这种并发症是另一种以反复发热发作为特征的疾病(即家族性地中海热)的典型特征,因此可以推测这两种罕见临床疾病之间存在重叠综合征。