Zuber M, Miesel R, Brandl B
German Research Center for Rheumatology, Berlin.
Clin Rheumatol. 1995 Jan;14(1):100-3. doi: 10.1007/BF02208093.
Reported is the case of a 60-year-old female who was referred to our rheumatology center because of a high titer of antinuclear antibodies (ANAs). Initially several lupus-like features suggested a diagnosis of undifferentiated connective tissue disease (UCTD). Immunofluorescence of the patient's serum showed a nuclear dot pattern. Counterimmunoelectrophoresis for antibodies to Sm, RNP, SS-A and SS-B were negative. Immunoblotting revealed a band at 53 kD which did not correspond to known autoantigens. Several months later the patient presented to the emergency room with symptoms due to a hypertensive crisis. Check-up finally revealed a cortisone-producing tumour of the right adrenal gland. The adenoma was removed by surgery and the patient did well again.
报告了一例60岁女性病例,该患者因抗核抗体(ANA)滴度高而被转诊至我们的风湿病中心。最初,一些狼疮样特征提示诊断为未分化结缔组织病(UCTD)。患者血清的免疫荧光显示核点模式。针对Sm、RNP、SS - A和SS - B抗体的对流免疫电泳均为阴性。免疫印迹显示一条53 kD的条带,其与已知自身抗原不符。几个月后,患者因高血压危象症状就诊于急诊室。最终检查发现右肾上腺有一个产生皮质醇的肿瘤。该腺瘤通过手术切除,患者恢复良好。