Saulsbury Frank T
Division of Immunology and Rheumatology, Department of Pediatrics, University of Virginia Health System, Charlottesville, Virginia 22908, USA.
J Pediatr. 2003 Jul;143(1):127-9. doi: 10.1016/S0022-3476(03)00212-9.
This report describes a boy with hyperimmunoglobulinemia D and periodic fever syndrome (HIDS). The serum IgD level was normal, but the serum IgA concentration was markedly elevated. In addition, he had a history of orchitis on two occasions, a previously unreported manifestation of HIDS. This report expands the clinical and laboratory features associated with HIDS and serves to emphasize that a normal serum IgD level does not exclude the diagnosis of HIDS.
本报告描述了一名患有高免疫球蛋白D血症和周期性发热综合征(HIDS)的男孩。血清IgD水平正常,但血清IgA浓度显著升高。此外,他有两次睾丸炎病史,这是HIDS一种此前未报告的表现。本报告扩展了与HIDS相关的临床和实验室特征,并强调血清IgD水平正常并不能排除HIDS的诊断。