Yamasaki Gentaro, Okano Mitsumasa, Nakayama Kazuhiko, Jimbo Naoe, Sendo Sho, Tamada Naoki, Misaki Kenta, Shinkura Yuto, Yanaka Kenichi, Tanaka Hidekazu, Akashi Kengo, Morinobu Akio, Yokozaki Hiroshi, Emoto Noriaki, Hirata Ken-Ichi
Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.
Department of Diagnostic Pathology, Kobe University Graduate School of Medicine, Japan.
Intern Med. 2019;58(4):593-601. doi: 10.2169/internalmedicine.1143-18. Epub 2019 Feb 15.
Rheumatoid vasculitis is a rare etiology for pulmonary hypertension (PH) in patients with connective tissue disease. We encountered a case of acute PH crisis in a case with rheumatoid vasculitis eight months after undergoing adalimumab reduction. Since no repetition of arthralgia occurred after the adalimumab reduction, we decided to not increase the dose of adalimumab. However, hemodynamic collapse thereafter developed and even though steroid pulse therapy was administered, the patient nevertheless died. The autopsy showed clusters of acute and chronic inflammation around the remodeled pulmonary arteries along with micro-thrombi in the vessel lumen. We should consider the possibility of critical worsening of PH as a phenotype of vasculitis related to immunosuppressive therapy reduction.
类风湿性血管炎是结缔组织病患者肺动脉高压(PH)的罕见病因。我们遇到一例类风湿性血管炎患者,在阿达木单抗减量八个月后发生急性PH危象。由于阿达木单抗减量后未再次出现关节痛,我们决定不增加阿达木单抗剂量。然而,此后发生了血流动力学崩溃,尽管给予了类固醇冲击治疗,患者仍死亡。尸检显示,重塑的肺动脉周围有急性和慢性炎症簇,血管腔内有微血栓。我们应考虑PH作为与免疫抑制治疗减量相关的血管炎表型严重恶化的可能性。