严重感染性休克患者鸟氨酸转甲氨基酶缺乏致死性高氨血症1例

J. Hwang, J. H. Song, Y. S. Lee, K. Chung, S. Kim, E. Y. Kim, J. Jung, Y. Kang, Y. S. Kim, Joon Chang, M. Park
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摘要

严重的高氨血症可由于尿素循环中遗传或获得性肝酶缺陷而发生,其中鸟氨酸转氨基甲酰基酶缺乏症(OTCD)是最常见的形式。我们报告一个非常罕见的病例,45岁的韩国男性因严重感染性休克并急性呼吸衰竭而被送入重症监护病房(ICU)。患者在ICU重症监护期间出现明显的高氨血症(> 1700 μg/dL),伴有突发性精神变化,导致危及生命的脑水肿。尽管进行了各种努力,包括持续的肾脏替代治疗和使用分子吸附剂再循环系统(体外肝脏支持-白蛋白透析)来降低他的血清氨水平,但患者没有康复。患者的致命性高氨血症后来被证明是获得性肝酶缺陷(OTCD)的一种表现,它是由严重的分解代谢条件引发的,如严重感染性休克合并急性呼吸衰竭。
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Lethal Hyperammonemia due to Ornithine Transcarbamylase Deficiency in a Patient with Severe Septic Shock
Severe hyperammonemia can occur as a result of inherited or acquired liver enzyme defects in the urea cycle, among which ornithine transcarbamylase deficiency (OTCD) is the most common form. We report a very rare case of a 45-year-old Korean male who was admitted to the intensive care unit (ICU) due to severe septic shock with acute respiratory failure caused by Pneumocystis jiroveci pneumonia. During his ICU stay with ventilator care, the patient suffered from marked hyperammonemia (>1,700 μg/dL) with abrupt mental change leading to life-threatening cerebral edema. Despite every effort including continuous renal replacement therapy and use of a molecular adsorbent recirculating system (extracorporeal liver support-albumin dialysis) to lower his serum ammonia level, the patient was not recovered. The lethal hyperammonemia in the patient was later proven to be a manifestation of acquired liver enzyme defect known as OTCD, which is triggered by serious catabolic conditions, such as severe septic shock with acute respiratory failure.
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