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巨 AST:患有 MCAD 缺乏症的青少年中的误导性发现。

Macro-AST: misleading finding in an adolescent with MCAD-deficiency.

机构信息

Department of Paediatrics, Hannover Medical School, Hannover, Germany.

出版信息

BMC Gastroenterol. 2012 Aug 30;12:119. doi: 10.1186/1471-230X-12-119.

Abstract

BACKGROUND

MCAD-deficiency is the most common inborn error of fatty acid oxidation now included in many newborn screening programms using MS/MS. During prolonged catabolic episodes, patients may suffer from metabolic decompensation with dysfunction of liver, skeletal- and heart muscle as well as brain. In anabolism, neither clinical symptoms nor biochemical signs of organ dysfunction occur.

CASE PRESENTATION

We report a female patient with MCAD-deficiency in whom at the age of 11 years isolated AST-elevation was found without any clinical or biochemical signs of organ dysfunction. We showed by polyethylene glycol precipitation that macro-AST formation was responsible for this biochemical finding. AST was probably complexed with immunoglobulins possibly related to an allergic disposition. Macro-AST formation is not a special feature of MCAD-deficiency but rather a non-specific, coincidental finding which also occurs in healthy individuals. The general practitioner consulted by the patient before coming to our outpatient clinic for inborn errors of metabolism was worried that isolated AST-elevation indicated cell damage in MCAD-deficiency. He ordered further diagnostic tests like ultrasound, ECG and echocardiography without any pathology.

CONCLUSION

In isolated AST-elevation, macro-AST has to be considered in order to avoid unnecessary, costly and invasive evaluation. This is not only true for healthy persons but for patients with chronic diseases like MCAD as well.

摘要

背景

现在,中链酰基辅酶 A 脱氢酶缺乏症(MCAD)是脂肪酸氧化中最常见的先天性缺陷,已被纳入许多使用 MS/MS 的新生儿筛查计划中。在长时间的分解代谢发作期间,患者可能会出现代谢失代偿,导致肝、骨骼肌和心肌以及大脑功能障碍。在合成代谢期间,既没有临床症状,也没有器官功能障碍的生化迹象。

病例介绍

我们报告了一名女性 MCAD 缺乏症患者,在 11 岁时发现孤立性 AST 升高,没有任何器官功能障碍的临床或生化迹象。我们通过聚乙二醇沉淀表明,巨 AST 的形成是导致这种生化发现的原因。AST 可能与免疫球蛋白复合物结合,可能与过敏体质有关。巨 AST 的形成不是 MCAD 缺乏症的特有特征,而是一种非特异性、偶然的发现,也发生在健康个体中。在来我们代谢门诊就诊之前,患者的全科医生担心孤立性 AST 升高表明 MCAD 缺乏症中的细胞损伤。他下令进行进一步的诊断测试,如超声、心电图和超声心动图,但没有任何病理学结果。

结论

在孤立性 AST 升高的情况下,必须考虑巨 AST,以避免不必要的、昂贵的和有创的评估。这不仅适用于健康人,也适用于患有慢性疾病(如 MCAD)的患者。

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Macroenzyme as a cause of unexplained elevation of aspartate aminotransferase.
Mayo Clin Proc. 1987 Aug;62(8):681-7. doi: 10.1016/s0025-6196(12)65219-7.

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