Chenxi Li , Xiangyuan Chen , Xilong Tang , Huasong Zeng , Juan Zhou
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引用次数: 0
摘要
高免疫球蛋白 D 综合征(HIDS)是一种罕见但严重的自身炎症性疾病,如果不及早诊断和治疗,预后很差。在此,我们报告了三例具有典型临床表现和明确遗传诊断的 HIDS 儿童病例。患者1反复发热,伴有斑丘疹。患者 2 表现为周期性发热、胆汁淤积、淋巴结病、口腔炎、关节痛和腹痛,并因肠梗阻接受了手术治疗。患者3是患者2的兄弟姐妹,出现周期性发热,因肠梗阻接受了手术治疗。这三名患者均接受了白细胞介素(IL)-6 受体拮抗剂(托西珠单抗)治疗。结果显示,妥昔单抗能有效减少炎症复发。早期诊断和替西利珠单抗治疗可有效改善HIDS患者的预后。
Tocilizumab effectively reduces flares of hyperimmunoglobulin D syndrome in children: Three cases in China
Hyperimmunoglobulin D syndrome (HIDS) is a rare but severe autoinflammatory disease with a poor prognosis if not diagnosed and treated early. Here, we report three cases of HIDS in children with typical clinical manifestations and a clear genetic diagnosis. Patient 1 experienced recurrent fever flares with a maculo-papular skin rash. Patient 2 presented with periodic fever, cholestasis, lymphadenopathy, aphthous stomatitis, arthralgia, and abdominal pain and underwent surgery for intestinal obstruction. Patient 3, a sibling of patient 2, presented with periodic fever and underwent a surgical procedure for intussusception. All three patients were administered interleukin (IL)-6 receptor antagonist (tocilizumab). The results showed that tocilizumab effectively reduced inflammatory flares. Early diagnosis and tocilizumab treatment are effective at improving the prognosis of HIDS patients.
期刊介绍:
Molecular Genetics and Metabolism Reports is an open access journal that publishes molecular and metabolic reports describing investigations that use the tools of biochemistry and molecular biology for studies of normal and diseased states. In addition to original research articles, sequence reports, brief communication reports and letters to the editor are considered.