Liver neoplasms in methylmalonic aciduria: An emerging complication.
Patrick FornyMichel HochuliYusof RahmanMaesha DeheragodaAchim WeberJulien BaruteauStephanie GrunewaldPublished in: Journal of inherited metabolic disease (2019)
Methylmalonic aciduria (MMA) is an inherited metabolic disease caused by methylmalonyl-CoA mutase deficiency. Early-onset disease usually presents with a neonatal acute metabolic acidosis, rapidly causing lethargy, coma, and death if untreated. Late-onset patients have a better prognosis but develop common long-term complications, including neurological deterioration, chronic kidney disease, pancreatitis, optic neuropathy, and chronic liver disease. Of note, oncogenesis has been reported anecdotally in organic acidurias. Here, we present three novel and two previously published cases of MMA patients who developed malignant liver neoplasms. All five patients were affected by a severe, early-onset form of isolated MMA (4 mut0 , 1 cblB subtype). Different types of liver neoplasms, that is, hepatoblastoma and hepatocellular carcinoma, were diagnosed at ages ranging from infancy to adulthood. We discuss pathophysiological hypotheses involved in MMA-related oncogenesis such as mitochondrial dysfunction, impairment of tricarboxylic acid cycle, oxidative stress, and effects of oncometabolites. Based on the intriguing occurrence of liver abnormalities, including neoplasms, we recommend close biochemical and imaging monitoring of liver disease in routine follow-up of MMA patients.
Keyphrases
- early onset
- end stage renal disease
- late onset
- chronic kidney disease
- ejection fraction
- oxidative stress
- peritoneal dialysis
- newly diagnosed
- prognostic factors
- randomized controlled trial
- risk assessment
- systematic review
- high resolution
- depressive symptoms
- drug induced
- blood brain barrier
- clinical practice
- fatty acid
- weight loss
- subarachnoid hemorrhage