Bastone P, Squifflet J-L, Marbaix E, Houssiau F
Rheumatology Department, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Bruxelles, Belgium.
Gynaecology Department, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Bruxelles, Belgium.
Clin Exp Rheumatol. 2015 Mar-Apr;33(2 Suppl 89):S-142-4. Epub 2015 May 26.
Granulomatosis with polyangiitis, formerly called Wegener's granulomatosis, is a disease for which the treatment options are increasing, with the recent publication of several studies concerning the use of rituximab. The disease typically involves the upper airways, lungs and kidneys, but other far less frequent localisations are possible. Here, we describe a case of isolated relapse of granulomatosis with polyangiitis affecting the uterine cervix and upper vagina which dramatically responded to rituximab therapy, after failure of methotrexate treatment. This is the first documented response to rituximab of gynaecological involvement in granulomatosis with polyangiitis.
肉芽肿性多血管炎,以前称为韦格纳肉芽肿病,随着最近几项关于利妥昔单抗使用的研究发表,其治疗选择正在增加。该疾病通常累及上呼吸道、肺部和肾脏,但也可能出现其他不太常见的部位。在此,我们描述了一例肉芽肿性多血管炎孤立性复发的病例,病变累及子宫颈和阴道上段,在甲氨蝶呤治疗失败后,对利妥昔单抗治疗有显著反应。这是肉芽肿性多血管炎累及妇科的病例中首次有文献记载的对利妥昔单抗的反应。