Alsultan Mohammad, Kliea Marwa, Hassan Qussai
Department of Nephrology, Damascus University- Faculty of Medicine, Damascus, Syria.
Nephrology Department, Damascus University- Faculty of Medicine, Omar Ibn Abdulaziz Street, Al Mazah, Damascus, Syria.
BMC Nephrol. 2025 Feb 25;26(1):97. doi: 10.1186/s12882-025-04030-5.
This study aimed to detail acute tubulointerstitial nephritis (ATIN) patients, from relevant clinical manifestations to outcomes.
We reviewed ATIN patients between 2018 and 2022. All demographic data, labs, biopsy findings, treatment protocols, and outcomes were reported.
ATIN was diagnosed in nine patients, eight by kidney biopsy and one clinically. Drug-induced ATIN (DI-ATIN) was reported in five patients, including rifampin (RIF), allopurinol, mesalamine, and two with cephalosporins. Severe ATIN resulted after the first dose of RIF aligned with liver injury, hemolysis, and thrombocytopenia. Also, mesalamine and allopurinol induced gradual kidney failure a few months after the drug initiation. A patient with Tubulointerstitial nephritis and uveitis (TINU) syndrome showed refractory uveitis presenting during glucocorticoids (GCs) tapering, which resolved quickly with azathioprine (AZA) when not responding to GCs reescalation. Among the rarest cases, ATIN induced by a kidney-limited sarcoidosis, G6PD patient with hemolysis induced ATIN, and isolated ATIN induced by ANCA-associated vasculitis (AAV) with positive C-ANCA, which the latter representing the first case in our country and the fourth case worldwide. Labs showed anemia (88.8%), ESR elevation (85.7%), microscopic hematuria (in all patients), pyuria (44.4%), and proteinuria (77.7%). Biopsies showed interstitial infiltrations mainly with lymphocytes and monocytes. Eosinophils were found in one biopsy and neutrophils showed in 4 biopsies (50%).
ATIN is a disease with a diagnostic challenge, thus clinicians should maintain a high suspicion for diagnosis. The combination of AKI with positive tests (especially abnormal urine sediment, ESR elevation, and anemia) may suggest ATIN diagnosis and further support the treatment initiation, particularly when kidney biopsy is unable to be performed or when the inciting agent is predictable.
本研究旨在详细阐述急性肾小管间质性肾炎(ATIN)患者从相关临床表现到预后的情况。
我们回顾了2018年至2022年间的ATIN患者。报告了所有人口统计学数据、实验室检查结果、活检结果、治疗方案及预后情况。
共诊断出9例ATIN患者,其中8例通过肾活检确诊,1例临床诊断。报告了5例药物性ATIN(DI-ATIN)患者,包括利福平(RIF)、别嘌醇、美沙拉嗪,以及2例头孢菌素所致者。首剂RIF后出现严重ATIN,并伴有肝损伤、溶血和血小板减少。此外,美沙拉嗪和别嘌醇在用药数月后导致逐渐肾衰竭。1例肾小管间质性肾炎合并葡萄膜炎(TINU)综合征患者在糖皮质激素(GCs)减量期间出现难治性葡萄膜炎,在GCs剂量增加无效时,使用硫唑嘌呤(AZA)后迅速缓解。在极为罕见的病例中,有肾脏局限性结节病所致的ATIN、G6PD患者溶血所致的ATIN,以及C-ANCA阳性的抗中性粒细胞胞浆抗体相关血管炎(AAV)所致的孤立性ATIN,后者为我国首例、全球第四例。实验室检查显示贫血(88.8%)、血沉升高(85.7%)、镜下血尿(所有患者均有)、脓尿(44.4%)和蛋白尿(77.7%)。活检显示间质浸润主要为淋巴细胞和单核细胞。1例活检发现嗜酸性粒细胞,有4例活检显示中性粒细胞(50%)。
ATIN是一种诊断具有挑战性的疾病,因此临床医生应高度怀疑以进行诊断。急性肾损伤(AKI)与阳性检查结果(尤其是异常尿沉渣、血沉升高和贫血)相结合可能提示ATIN诊断,并进一步支持开始治疗,特别是在无法进行肾活检或诱发因素可预测时。