Pomponio Giovanni, Olivari Diletta, Mattioli Massimo, Angeletti Alessia, Rossetti Giulia, Goteri Gaia, Gabrielli Armando
Clinica Medica, Ospedali Riuniti Clinica Medica Section of Pathological Anatomy, Università Politecnica delle Marche, Ospedali Riuniti, Ancona, Italy.
Medicine (Baltimore). 2018 Jun;97(26):e11143. doi: 10.1097/MD.0000000000011143.
IgG4-related disease (IgG4-RD) is an emerging immune-mediated disease characterized by multi-organ involvement and variable clinical behavior.
We describe the case of a 50-year-old woman affected by a rare variant of IgG4-RD, characterized by eyelid xanthelasmas, adult-onset asthma and salivary and lacrimal glands enlargement. Multiple lymphadenopathies and a pulmonary mass were present at initial evaluation.
After a single course of rituximab (2g in 2 refracted doses), an almost complete clinical remission was achieved without chronic steroid administration.
Magnetic resonance imaging (MRI), high-resolution computed tomography (HRCT) of the thorax, and positron emission tomography (18FDG-PET-CT) confirmed good response to treatment. Circulating plasmablasts dropped to undetectable levels as well. Xanthelasmas only remained unchanged. Remission persisted at 1-year follow-up.
Steroid therapy is still considered standard first-line therapy in IgG4-RD. However, high doses are generally required and relapses are common during the tapering phase. Rituximab is a well described steroid-sparing strategy, so far reserved to refractory cases only. In our experience, rituximab has been used as first-line monotherapy, showing great and sustained efficacy and optimal tolerability. The peculiar variant of IgG4-RD affecting our patient, the relatively low baseline plasmablast concentration, and the early placement of rituximab therapy may have facilitated the good response.
IgG4相关疾病(IgG4-RD)是一种新出现的免疫介导性疾病,其特征为多器官受累且临床行为多变。
我们描述了一名50岁女性患者的病例,她患有IgG4-RD的一种罕见变体,其特征为眼睑黄斑瘤、成人起病的哮喘以及唾液腺和泪腺肿大。初始评估时存在多处淋巴结病和一个肺部肿块。
在接受一个疗程的利妥昔单抗(分2次静脉滴注,共2g)治疗后,未使用慢性类固醇药物即实现了几乎完全的临床缓解。
磁共振成像(MRI)、胸部高分辨率计算机断层扫描(HRCT)以及正电子发射断层扫描(18FDG-PET-CT)证实对治疗反应良好。循环浆母细胞也降至检测不到的水平。仅黄斑瘤保持不变。1年随访时缓解持续存在。
类固醇疗法仍被视为IgG4-RD的标准一线疗法。然而,通常需要高剂量,且在减量阶段复发很常见。利妥昔单抗是一种已被充分描述的类固醇节省策略,迄今为止仅用于难治性病例。根据我们的经验,利妥昔单抗已被用作一线单药治疗,显示出巨大且持续的疗效以及最佳的耐受性。影响我们这位患者的IgG4-RD的特殊变体、相对较低的基线浆母细胞浓度以及利妥昔单抗治疗的早期应用可能促进了良好的反应。