Recurrent acute pancreatitis in a patient with acquired glutaric aciduria type II: a case report

Authors

  • Lalita M. Andersen Department of Surgery, Mater Public Hospital, South Brisbane, QLD, Australia
  • Jade Enoch Department of Surgery, Mater Public Hospital, South Brisbane, QLD, Australia
  • Trent Cross Department of Surgery, Mater Public Hospital, South Brisbane, QLD, Australia

DOI:

https://doi.org/10.18203/2349-2902.isj20250741

Keywords:

Acquired metabolic disorders, Glutaric aciduria type II, Hepatobiliary surgery, Multiple acyl-CoA dehydrogenase deficiency, Pancreatitis

Abstract

Acquired glutaric aciduria type II (GAII) is an emerging metabolic disorder linked to mitochondrial dysfunction, which may predispose patients to recurrent pancreatitis due to impaired fatty acid metabolism. This report presents the first documented instance of recurrent acute pancreatitis in a patient with acquired GAII. A 30-year-old Caucasian female with a known diagnosis of acquired GAII presented with recurrent episodes of acute pancreatitis, including two episodes during pregnancy and one outside pregnancy. Thorough investigations systematically excluded common causes such as gallstones, alcohol use, hypertriglyceridemia, IgG4-related disease, autoimmune pancreatitis and anatomical anomalies. Management required multidisciplinary collaboration involving surgeons, obstetricians, metabolic specialists and medical physicians. Treatment involved conservative surgical management including intravenous fluid resuscitation, analgesia, anti-emetics and specialized metabolic support, particularly intravenous dextrose while fasting. This case highlights the importance of recognizing acquired GAII as a potential underlying cause of recurrent acute pancreatitis. Awareness among surgical and multidisciplinary teams is crucial for timely diagnosis and effective management to prevent severe complications.

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References

Prasun P. Multiple acyl-CoA dehydrogenase deficiency. In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews®. Seattle (WA): University of Washington, Seattle. Available at: https://www.ncbi.nlm.nih.gov. Accessed on 21 September 2024.

Coşkun T, Köksal N, Kalkanoğlu HS. Acute pancreatitis in a patient with glutaric acidemia type II. Turk J Pediatr. 1997;39(3):379-85.

Liang WC, Ohkubo K, Yamamoto T. Riboflavin-responsive glutaric aciduria type II with recurrent pancreatitis. Pediatr Neurol. 2004;31(3):218-21. DOI: https://doi.org/10.1016/j.pediatrneurol.2004.02.015

Elkhateeb N, Al-Jishi E, Al-Jishi M. Pancreatitis in multiple acyl CoA dehydrogenase deficiency: an underdiagnosed complication. JIMD Rep. 2020;57(1):15-22. DOI: https://doi.org/10.1002/jmd2.12175

Gapp J, Tariq A, Chandra S. Acute Pancreatitis. In: StatPearls. Treasure Island (FL): StatPearls Publishing. Available at: https://www.ncbi.nlm. nih.gov. Accessed on 27 November 2024.

Finsterer J, Frank M. Gastrointestinal manifestations of mitochondrial disorders: a systematic review. Ther Adv Gastroenterol. 2017;10(2):142-54. DOI: https://doi.org/10.1177/1756283X16666806

Ingoglia F, Tanfous M, Ellezam B. MADD-like pattern of acylcarnitines associated with sertraline use. Mol Genet Metab Rep. 2024;41:101142. DOI: https://doi.org/10.1016/j.ymgmr.2024.101142

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Published

2025-03-19

How to Cite

Andersen, L. M., Enoch, J., & Cross, T. (2025). Recurrent acute pancreatitis in a patient with acquired glutaric aciduria type II: a case report. International Surgery Journal, 12(4), 633–636. https://doi.org/10.18203/2349-2902.isj20250741

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Section

Case Reports