Encephalopathy After a High-Dose Dexamethasone Suppression Test in a Woman With X-Linked Ornithine Transcarbamylase Deficiency

被引:1
作者
Seol, Hyunho
Hong, Yoon Hee [1 ]
Jeon, Min Ji [2 ,3 ]
机构
[1] Univ Ulsan, Asan Med Ctr, Dept Internal Med, Coll Med, Seoul, South Korea
[2] Eulji Univ, Uijeongbu Eulji Med Ctr, Dept Neurol, Sch Med, Uijongbu, South Korea
[3] Univ Ulsan, Asan Med Ctr, Dept Internal Med, Div Endocrinol & Metab,Coll Med, Seoul, South Korea
关键词
ornithine transcarbamylase deficiency; deficiency hyperammonemic encephalopathy; high-dose dexamethasone; suppression test; mild autonomous cortisol secretion;
D O I
10.1016/j.aace.2024.01.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Objective: The high-dose dexamethasone suppression test is a common and usually benign endocrine procedure. We report a patient with ornithine transcarbamylase deficiency (OTCD) who developed hyperammonemic encephalopathy after a high-dose dexamethasone suppression test. Case Report: A 46-year-old woman with a 1.3-cm right adrenal incidentaloma causing mild autonomous cortisol secretion underwent a high-dose dexamethasone suppression test for confirming adrenocorticotropic hormone independency. On the next day, she presented to the emergency room with confusion and somnolence. Her Glasgow Coma Scale score was 10 on arrival. The initial laboratory results showed ammonia, alanine transaminase, creatinine, and blood urea nitrogen levels of 289.51 (18.73-54.5) m g/dL, 21 (<= 33) <= 33) IU/L, 0.6 (0.6-1.1) mg/dL, and 13 (7-20) mg/dL, respectively. Electroencephalography showed triphasic morphology with no pathologies on brain imaging. Her husband told us that her brother and son had died in the neonatal period. On further review of medical records, we found that she was diagnosed as an OTCD carrier. We administered L-arginine, L-carnitine, rifaximin, and continuous renal replacement therapy. After 3 days, the serum ammonia level was 78.34 m g/dL with an increased Glasgow Coma Scale score of 15, and electroencephalography abnormalities disappeared. Discussion: Liver diseases and urea cycle disorders are the leading causes of hyperammonemia. This causes encephalopathy and death if the ammonia levels are too high. X-linked OTCD urea cycle disorder affects men more severely as they have only the carrier X chromosome. Glucocorticoids can exacerbate this disorder because they increase protein substrates converted to ammonia. Conclusion: This case reminds that it may be particularly important to have a complete medical history when administering glucocorticoids. (c) 2024 AACE. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:71 / 74
页数:4
相关论文
共 9 条
[1]   Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatment [J].
Cavicchi, Catia ;
Donati, Maria Alice ;
Parini, Rossella ;
Rigoldi, Miriam ;
Bernardi, Mauro ;
Orfei, Francesca ;
Silveri, Nicolo Gentiloni ;
Colasante, Aniello ;
Funghini, Silvia ;
Catarzi, Serena ;
Pasquini, Elisabetta ;
La Marca, Giancarlo ;
Mooney, Sean David ;
Guerrini, Renzo ;
Morrone, Amelia .
ORPHANET JOURNAL OF RARE DISEASES, 2014, 9
[2]   Survival after treatment with phenylacetate and benzoate for urea-cycle disorders [J].
Enns, Gregory M. ;
Berry, Susan A. ;
Berry, Gerard T. ;
Rhead, William J. ;
Brusilow, Saul W. ;
Hamosh, Ada .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (22) :2282-2292
[3]   Severe Hyperammonemia in Late-Onset Ornithine Transcarbamylase Deficiency Triggered by Steroid Administration [J].
Gascon-Bayarri, Jordi ;
Campdelacreu, Jaume ;
Estela, Jordi ;
Rene, Ramon .
CASE REPORTS IN NEUROLOGICAL MEDICINE, 2015, 2015
[4]   Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids [J].
Lipskind, S. ;
Loanzon, S. ;
Simi, E. ;
Ouyang, D. W. .
JOURNAL OF PERINATOLOGY, 2011, 31 (10) :682-684
[5]   Effects of high doses of glucocorticoids on free amino acids, ribosomes and protein turnover in human muscle [J].
Löfberg, E ;
Gutierrez, A ;
Wernerman, J ;
Anderstam, B ;
Mitch, WE ;
Price, SR ;
Bergström, J ;
Alvestrand, A .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2002, 32 (05) :345-353
[6]  
Longo N, 2022, Harrison's Principles of Internal Medicine, V21, P3268
[7]  
Meisenberg G, 2017, Principles of Medical Biochemistry, V4, P463
[8]  
Roberts DL, 2013, Case Rep Crit Care, V2013
[9]   Unmasked adult-onset urea cycle disorders in the critical care setting [J].
Summar, ML ;
Barr, F ;
Dawling, S ;
Smith, W ;
Lee, B ;
Singh, RH ;
Rhead, WJ ;
King, LS ;
Christman, BW .
CRITICAL CARE CLINICS, 2005, 21 (04) :S1-+