Alport综合征合并妊娠相关非典型溶血性尿毒症综合征合并月牙状肾小球肾炎1例。

Ilay Berke Mentese, Murat Tugcu, Ismail Nazli, Deniz Filinte, Ebru Asicioglu, Hakki Arikan, Serhan Tuglular, Arzu Velioglu
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摘要

妊娠期肾脏功能可能因各种原因而受损,妊娠期的生理变化可能暴露或加重已有的肾脏疾病。在此,我们报告一位孕妇出现肾范围蛋白尿。她后来出现急性肾损伤和先兆子痫。然而,分娩后,溶血性贫血和血小板减少症持续存在,她被诊断为非典型溶血性尿毒症综合征(aHUS)。虽然血液学异常在eculizumab治疗下得到了解决,但她的肾功能没有改善。肾活检显示月牙状肾小球肾炎,无血栓性微血管病变特征。同时,她被评估为听力障碍,并通过基因检测确诊为阿尔波特综合征。妊娠期Alport综合征患者的肾功能可能会恶化。然而,月牙状肾小球肾炎(GN)在阿尔波特病中是一种罕见的发现。Pauci-immune crescent GN已被证明与替代补体通路激活失调有关,这也是aHUS的潜在病理生理机制。
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A case of Alport syndrome with pregnancy-related atypical hemolytic uremic syndrome and crescentic glomerulonephritis.

Kidney function may be impaired during pregnancy due to various reasons, and the physiological changes of pregnancy may unmask or worsen pre-existing kidney disease. Herein, we report a pregnant patient presenting with nephrotic-range proteinuria. She later developed acute kidney injury and pre-eclampsia. However, hemolytic anemia and thrombocytopenia persisted after delivery, and she was diagnosed with atypical hemolytic uremic syndrome (aHUS). Although hematological abnormalities resolved with eculizumab treatment, her renal functions did not improve. Kidney biopsy showed crescentic glomerulonephritis without thrombotic microangiopathy features. Concurrently, she was evaluated for hearing impairment, and a diagnosis of Alport syndrome was confirmed with genetic testing. Kidney function may worsen in patients with Alport syndrome during pregnancy. However, crescentic glomerulonephritis (GN) is a rare finding in Alport disease. Pauci-immune crescentic GN has been shown to be related to dysregulated activation of the alternative complement pathway, which is also the underlying pathophysiological mechanism in aHUS.

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