AA Amyloidosis Secondary to Horton's Disease Complicated by Pulmonary Fibrosis: A Very Challenging Diagnosis and Therapy

M. Njie, P. M. Mulendelé, O. Mokni, M. Boutar, M. Haboub, S. Arous, M. Benouna, A. Drighil, L. Azzouzi, R. Habbal
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Abstract

AA amyloidosis is a classic and serious complication of many chronic inflammatory processes, whether of infectious, autoimmune, or neoplastic origin. It is frequently complicated by kidney damage, often in the form of a nephrotic syndrome. Giant cell arteritis is a common inflammatory arteritis in the elderly; however, it rarely causes AA amyloidosis. We report a rare case of Horton disease causing AA amyloidosis in an elderly patient with history of myopericarditis and repeated episodes of congestive heart failure. Patient was treated initially with dual therapy based on corticosteroids and anti TNF therapy (Tocilizumab) associated with heart failure therapy recommended by the European society of cardiology (ESC 2021 guidelines on Heart Failure). The initial outcome was favorable but later complicated by the involvement of the lungs; pulmonary fibrosis, responsible for repeated episodes of pleural effusion non controlled in spite of high dose of loop diuretics and repeated pleural punction. Patient died shortly after her second hospitalization due to respiratory insufficiency.
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继发于霍顿病并发肺纤维化的AA淀粉样变:一个非常具有挑战性的诊断和治疗
AA淀粉样变是许多慢性炎症过程的典型且严重的并发症,无论是感染性、自身免疫性还是肿瘤起源。它经常并发肾脏损害,通常以肾病综合征的形式出现。巨细胞动脉炎是老年人常见的炎症性动脉炎;然而,它很少引起AA淀粉样变。我们报告一个罕见的霍顿病引起AA淀粉样变的老年患者心包炎病史和反复发作的充血性心力衰竭。患者最初接受基于皮质类固醇和抗肿瘤坏死因子治疗(Tocilizumab)的双重治疗,与欧洲心脏病学会(ESC 2021心力衰竭指南)推荐的心力衰竭治疗相关。最初的结果是有利的,但后来因累及肺部而复杂化;肺纤维化,导致反复发作的胸腔积液,尽管高剂量的利尿剂和反复胸腔穿刺无法控制。患者在第二次住院后不久因呼吸功能不全死亡。
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