DOI QR코드

DOI QR Code

신생아의 심한 일과성 고암모니아혈증 1례

A case of severe transient hyperammonemia in a newborn

  • 황민우 (원광대학교 의과대학 소아과학교실) ;
  • 유승택 (원광대학교 의과대학 소아과학교실) ;
  • 오연균 (원광대학교 의과대학 소아과학교실)
  • Hwang, Min-Woo (Department of Pediatrics, Wonkwang University School of Medicine) ;
  • Yu, Seung-Taek (Department of Pediatrics, Wonkwang University School of Medicine) ;
  • Oh, Yeon-Kyun (Department of Pediatrics, Wonkwang University School of Medicine)
  • 투고 : 2010.01.31
  • 심사 : 2010.03.02
  • 발행 : 2010.04.15

초록

신생아 일과성 고암모니아혈증은 고암모니아혈증을 특징으로 하며 대부분 호흡곤란 치료를 받는 미숙아에서 발생한다. 발생원인은 정확히 알려져 있지 않으나 생후 2-3일에 호흡 곤란, 기면, 경련, 혼수 등의 임상 증상을 보이고, 생화학적 검사 상 혈중암모니아 농도가 현저히 증가하며 요소회로 효소 치는 정상을 보인다. 치료가 늦으면 사망에 이르는 응급을 요하는 질환이나 즉각적이고 적절한 치료 시 신경학적 손상을 남기지 않고 호전 가능하다. 저자들은 호흡곤란을 보여 호흡기 치료를 받던 35주 미숙아에서 48시간 내에 경련과 함께 혼수상태에 빠지고 검사상 고암모니아혈증을 보여 신투석 등의 치료 후 회복되었으며 2년 추적관찰에서 정상을 보인 환아를 보고하는 바이다.

Transient hyperammonemia in a newborn is an overwhelming disease manifested by hyperammonemic coma. The majority of affected newborns are premature and have mild respiratory syndrome. The diagnosis may be difficult to determine. This metabolic disorder is primarily characterized by severe hyperammonemia in the postnatal period, coma, absence of abnormal organic aciduria and normal activity of the enzymes of the urea cycle. Hyperammonemic coma may develop within 2-3 days of life, although its etiology is unknown. Laboratory studies reveal marked hyperammonemia (>$4,000{\mu}mol/L$). The degree of neurologic impairment and developmental delay in this disorder depends on the duration of hyperammonemic coma. Moreover, the infant may succumb to the disease if treatment is not started immediately and continued vigorously. Hyperammonemic coma as a medical emergency requires dialysis therapy. Here, we report a case of severe transient hyperammonemia in a preterm infant (35 week of gestation) presented with respiratory distress, seizure, and deep coma within 48 hours and required ventilatory assistance and marked elevated plasma ammonia levels. He survived with aggressive therapy including peritoneal dialysis, and was followed 2 years later without sequelae.

키워드

참고문헌

  1. Burton B. Pediatric liver: helping adults by treating children. Urea cycle disorders. Clin Liver Dis 2000;4:1-13. https://doi.org/10.1016/S1089-3261(05)70094-5
  2. Iraj R, Urea Clycle and Hyperammonemia. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF. Nelson textbook of pediatrics. 18th ed. Philadelphia: WB Saunders Co, 2007:561.
  3. Gerard TB. Inborn Errors of Carbohydrate, Ammonia, Amino Acid, and Organic Acid Metabolism. In: Taeusch HW, Ballard RA, Gleason CA. Avery's diseases of the newborn. 8th ed. Philadelphia: Elsevier Sanders Co, 2005:234-5.
  4. Choi JY, Lee SH, Jun SS, Seo SS. A case of transient hyperammonemia of the newborn infant. J Korean Soc Neonatal 2001;8:156-60.
  5. Snyderman SE. Clinical aspects of disorders of the urea cycle. Pediatrics 1981;68:284-9.
  6. Ballard RA, Vinocur B, Reynolds JW, Wennberg RP, Merritt A, Sweetman L, et al. Transient hyperammonemia of the preterm infant. N Engl J Med 1978;299:920-5. https://doi.org/10.1056/NEJM197810262991704
  7. Ellison PH, Cowger ML. Transient hyperammonemia in the preterm infant.: neurologic aspects. Neurology 1981;31:767- 70. https://doi.org/10.1212/WNL.31.6.767
  8. Giacoia GP, Padilla-Lugo A. Severe transient neonatal hyperammonemia. Am J Perinatol 1986;3:249-54. https://doi.org/10.1055/s-2007-999877
  9. Whitelaw A, Bridges S, Leaf A, Evans D. Emergency treatment of neonatal hyperammonemic coma with systemic hypothermia. Lancet 2001;358:36-8. https://doi.org/10.1016/S0140-6736(00)05269-7
  10. Stojanovic VD, Doronjski AR, Barisic N, Kovacevic BB, Paviovic VS. A case of transient hyperammonemia in a newborn. J Matern Fetal Neonatal Med 2009;31:1-4.
  11. Goldberg RN, Cabal LA, Sinatra FR, Plajstek CE, Hodgman JE. Hyperammonemia associated with perinatal asphyxia. Pediatrics 1979;64:336-41.
  12. Walser M. Urea cycle disorders and other hereditary hyperammonemia syndromes. In: Stanbury JB, Wyngaarden JB, Frederickson DS, Goldstein JL, Brown MS, editors. The metabolic basis of inherited disease. 5th ed. New York: McGraw-Hill, 1983:402-38.
  13. Beddis IR, Hughes EA, Rosser E, Fenton JC. Plasma ammonia levels in newborn infants admitted to an intensive care baby unit. Arch Dis Child 1980;55:516-20. https://doi.org/10.1136/adc.55.7.516
  14. Krishnan L, Diwakar KK, Patil P, Bhaskaranand N. Transient hyperammonemia of newborn. Indian J Pediatr 1996;63:113- 6. https://doi.org/10.1007/BF02823880
  15. Yoshino M, Sakaguchi Y, Kuriya N, Ohtani Y, Yamashita F, Hashimoto T, et al. A nationwide survey on transient hyperammonemia in newborn infants in Japan: prognosis of life and neurological outcome. Neuropediatrics 1991;22:198-202. https://doi.org/10.1055/s-2008-1071441
  16. Rajpoot DK, Gargus JJ. Acute hemodialysis for hyperammonemia in small neonates. Pediatr Nephrol 2004;19:390-5. https://doi.org/10.1007/s00467-003-1389-5
  17. Summar M, Pietsch J, Deshpande J, Schulman G. Effective hemodialysis and hemofiltration driven by an extracorporeal membrane oxygenation pump in infants with hyperammonemia. J Pediatr 1996;128:379-82. https://doi.org/10.1016/S0022-3476(96)70287-1
  18. Batshaw ML. Inborn errors of urea synthesis. Ann Neurol 1994;35:133-41. https://doi.org/10.1002/ana.410350204
  19. Cleary MA, Green A. Developmental delay: when to suspect and how to investigate for an inborn error of metabolism. Arch Dis Child 2005;90:1128-32. https://doi.org/10.1136/adc.2005.072025