Dugowson C E, Aitken M L
Department of Medicine, University of Washington, Seattle.
Chest. 1991 Mar;99(3):781-4. doi: 10.1378/chest.99.3.781.
A 65-year-old woman presented with recurrent Wegener's granulomatosis following two years of immunosuppressive therapy and three years of complete remission. At her initial presentation, she had a characteristic x-ray picture showing multiple nodules with total resolution of these findings at three months. Five years later, at the time of clinical relapse, her chest x-ray film showed bilateral diffuse infiltrative disease. This change in radiologic presentation upon relapse of Wegener's has not previously been reported. Other unusual features include diffuse infiltrates as the pulmonary presentation and the long interval between cessation of therapy and relapse. We review the radiologic manifestations of Wegener's granulomatosis.
一名65岁女性在接受了两年免疫抑制治疗并完全缓解三年后,出现复发性韦格纳肉芽肿。初次就诊时,她的X线表现具有特征性,显示多个结节,这些表现三个月时完全消退。五年后,临床复发时,她的胸部X线片显示双侧弥漫性浸润性病变。韦格纳肉芽肿复发时放射学表现的这种变化此前未见报道。其他不寻常的特征包括以弥漫性浸润作为肺部表现以及治疗停止与复发之间的间隔时间长。我们回顾了韦格纳肉芽肿的放射学表现。