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迟发性多种酰基辅酶A脱氢酶缺乏症(MADD)的肝脏表现:病例报告与系统评价

Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review.

作者信息

Siano Maria Anna, Mandato Claudia, Nazzaro Lucia, Iannicelli Gennaro, Ciccarelli Gian Paolo, Barretta Ferdinando, Mazzaccara Cristina, Ruoppolo Margherita, Frisso Giulia, Baldi Carlo, Tartaglione Salvatore, Di Salle Francesco, Melis Daniela, Vajro Pietro

机构信息

Postgraduate School of Pediatrics, Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.

Unit of Pediatrics 1, AORN Santobono-Pausilipon, Naples, Italy.

出版信息

Front Pediatr. 2021 May 10;9:672004. doi: 10.3389/fped.2021.672004. eCollection 2021.

Abstract

Diagnosis of pediatric steatohepatitis is a challenging issue due to a vast number of established and novel causes. Here, we report a child with Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) presenting with an underrated muscle weakness, exercise intolerance and an atypically severe steatotic liver involvement. A systematic literature review of liver involvement in MADD was performed as well. Our patient is a 11-year-old otherwise healthy, non-obese, male child admitted for some weakness/asthenia, vomiting and recurrent severe hypertransaminasemia (aspartate and alanine aminotransferases up to ×20 times upper limit of normal). Hepatic ultrasound showed a bright liver. MRI detected mild lipid storage of thighs muscles. A liver biopsy showed a micro-macrovacuolar steatohepatitis with minimal fibrosis. Main causes of hypertransaminasemia were ruled out. Serum aminoacids (increased proline), acylcarnitines (increased C4-C18) and a large excretion of urinary glutaric acid, ethylmalonic, butyric, isobutyric, 2-methyl-butyric and isovaleric acids suggested a diagnosis of MADD. Serum acylcarnitines and urinary organic acids fluctuated overtime paralleling serum transaminases during periods of illness/catabolic stress, confirming their recurrent nature. Genetic testing confirmed the diagnosis [homozygous c.1658A > G (p.Tyr553Cys) in exon 12 of the ETFDH gene]. Lipid-restricted diet and riboflavin treatment rapidly ameliorated symptoms, hepatic ultrasonography/enzymes, and metabolic profiles. Literature review (37 retrieved eligible studies, 283 patients) showed that liver is an extramuscular organ rarely involved in late-onset MADD (70 patients), and that amongst 45 patients who had fatty liver only nine had severe presentation. MADD is a disorder with a clinically heterogeneous phenotype. Our study suggests that MADD warrants consideration in the work-up of obesity-unrelated severe steatohepatitis.

摘要

由于存在大量已知和新发现的病因,小儿脂肪性肝炎的诊断是一个具有挑战性的问题。在此,我们报告一名患有多种酰基辅酶A脱氢酶缺乏症(MADD)的儿童,其表现为未被充分认识的肌肉无力、运动不耐受以及非典型的严重脂肪性肝脏受累。我们还对MADD患者肝脏受累情况进行了系统的文献综述。我们的患者是一名11岁的健康、非肥胖男性儿童,因出现一些虚弱/乏力、呕吐及反复严重的转氨酶升高(天冬氨酸和丙氨酸转氨酶高达正常上限的20倍)入院。肝脏超声显示肝脏回声增强。MRI检测到大腿肌肉有轻度脂质蓄积。肝活检显示为微大泡性脂肪性肝炎,纤维化程度轻微。排除了导致转氨酶升高的主要原因。血清氨基酸(脯氨酸升高)、酰基肉碱(C4 - C18升高)以及尿中大量排泄戊二酸、乙基丙二酸、丁酸、异丁酸、2 - 甲基丁酸和异戊酸提示诊断为MADD。在疾病/分解代谢应激期间,血清酰基肉碱和尿有机酸随时间波动,与血清转氨酶平行,证实了它们的反复性。基因检测确诊了该诊断[ETFDH基因第12外显子纯合子c.1658A > G(p.Tyr553Cys)]。低脂饮食和核黄素治疗迅速改善了症状、肝脏超声/酶学及代谢指标。文献综述(检索到37项符合条件的研究,共283例患者)显示,肝脏是晚期MADD(70例患者)中很少受累的肌肉外器官,在45例脂肪肝患者中,只有9例表现严重。MADD是一种临床表型异质性的疾病。我们的研究表明,在评估与肥胖无关的严重脂肪性肝炎时,应考虑MADD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3070/8143529/a82408e7a4a0/fped-09-672004-g0001.jpg

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