Rosenberg A M, Petty R E
Arthritis Rheum. 1982 Sep;25(9):1041-7. doi: 10.1002/art.1780250902.
Thirty-nine children with a syndrome of seronegative enthesopathy and arthropathy were evaluated. The group included 25 patients with no apparent underlying primary disease and 13 with either ankylosing spondylitis, inflammatory bowel disease, reactive arthritis, or Reiter's syndrome. Significant distinguishing characteristics of the group included male predominance, late age at onset, positive family histories of arthritis, oligoarthropathy, axial skeleton involvement, and the presence of the B27 histocompatibility antigen. This syndrome is distinguishable from other childhood rheumatic disorders, including juvenile rheumatoid arthritis. Its recognition may reliably identify children with the prodromal manifestations of seronegative spondylarthropathies.
对39名患有血清阴性附着点病和关节病综合征的儿童进行了评估。该组包括25名无明显潜在原发性疾病的患者以及13名患有强直性脊柱炎、炎性肠病、反应性关节炎或赖特综合征的患者。该组显著的鉴别特征包括男性占优势、发病年龄较晚、关节炎家族史阳性、少关节炎、中轴骨骼受累以及存在B27组织相容性抗原。这种综合征可与其他儿童风湿性疾病相鉴别,包括幼年类风湿关节炎。对其识别可可靠地鉴别出具有血清阴性脊柱关节病前驱表现的儿童。