메뉴 건너뛰기




Volumn 105, Issue 4, 2014, Pages 243-249

Neonatal hemolytic jaundice: Morphologic features of erythrocytes that will help you diagnose the underlying condition

Author keywords

Erythrocyte; Glucose 6 phosphate dehydrogenase; Hemolysis; Jaundice; Kernicterus; Neonate

Indexed keywords

BITE CELL; BLISTER CELL; BLOOD; CELL STRUCTURE; CELL TYPE; ECHINOCYTE; ELLIPTOCYTE; ERYTHROCYTE; ERYTHROCYTE MEMBRANE; GENE MUTATION; GENE SEQUENCE; HEMOLYSIS; HUMAN; MICROSPHEROCYTE; NEONATAL HYPERBILIRUBINEMIA; NEONATOLOGIST; NEWBORN; NEWBORN HEMOLYTIC DISEASE; NEWBORN JAUNDICE; PRIORITY JOURNAL; REVIEW; TECHNOLOGY; BLOOD EXAMINATION; ERYTHROCYTE DISORDER; GENETIC PREDISPOSITION; GENETICS; HYPERBILIRUBINEMIA, NEONATAL; JAUNDICE, NEONATAL; MICROSCOPY; PATHOLOGY; PREDICTIVE VALUE; PROGNOSIS; RISK FACTOR; SEVERITY OF ILLNESS INDEX; BLOOD GROUP ABO INCOMPATIBILITY; ELLIPTOCYTOSIS; ENZYME DEFICIENCY; ERYTHROCYTE STRUCTURE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEALTH CARE COST; HEMANGIOMA; HEMOLYTIC UREMIC SYNDROME; HEREDITARY SPHEROCYTOSIS; HYPERBILIRUBINEMIA; JAUNDICE; KERNICTERUS; MORPHOLOGY; NEWBORN CARE; NEWBORN SEPSIS; PERINATAL ASPHYXIA; PROTEIN C DEFICIENCY; THROMBOCYTOPENIA; THROMBOTIC THROMBOCYTOPENIC PURPURA; VASCULAR TUMOR;

EID: 84893683831     PISSN: 16617800     EISSN: 16617819     Source Type: Journal    
DOI: 10.1159/000357378     Document Type: Review
Times cited : (45)

References (42)
  • 1
    • 84874658740 scopus 로고    scopus 로고
    • Initial clinical testing evaluation and risk assessment for universal screening for hyperbilirubinemia Study Group. Predischarge screening for severe neonatal hyperbilirubinemia identifies infants who need phototherapy
    • Bhutani VK, Stark AR, Lazzeroni LC, Poland R, Gourley GR, Kazmierczak S, Meloy L, Burgos AE, Hall JY, Stevenson DK: Initial clinical testing evaluation and risk assessment for universal screening for hyperbilirubinemia Study Group. Predischarge screening for severe neonatal hyperbilirubinemia identifies infants who need phototherapy. J Pediatr 2013; 162: 477-482.e1.
    • (2013) J Pediatr , vol.162
    • Bhutani, V.K.1    Stark, A.R.2    Lazzeroni, L.C.3    Poland, R.4    Gourley, G.R.5    Kazmierczak, S.6    Meloy, L.7    Burgos, A.E.8    Hall, J.Y.9    Stevenson, D.K.10
  • 2
    • 79957938585 scopus 로고    scopus 로고
    • The need for technologies to prevent bilirubin-induced neurologic dysfunction syndrome
    • Bhutani VK, Stevenson DK: The need for technologies to prevent bilirubin-induced neurologic dysfunction syndrome. Semin Perinatol 2011; 35: 97-100.
    • (2011) Semin Perinatol , vol.35 , pp. 97-100
    • Bhutani, V.K.1    Stevenson, D.K.2
  • 5
    • 18544409633 scopus 로고    scopus 로고
    • Imbalance between production and conjugation of bilirubin: A fundamental concept in the mechanism of neonatal jaundice
    • Kaplan M, Muraca M, Hammerman C, Rubaltelli FF, Vilei MT, Vreman HJ, Stevenson DK: Imbalance between production and conjugation of bilirubin: a fundamental concept in the mechanism of neonatal jaundice. Pediatrics 2002; 110:e47-e49.
    • (2002) Pediatrics , vol.110
    • Kaplan, M.1    Muraca, M.2    Hammerman, C.3    Rubaltelli, F.F.4    Vilei, M.T.5    Vreman, H.J.6    Stevenson, D.K.7
  • 6
    • 33746815798 scopus 로고    scopus 로고
    • The contribution of hemolysis to early jaundice in normal newborns
    • Maisels MJ, Kring E: The contribution of hemolysis to early jaundice in normal newborns. Pediatrics 2005; 118: 276-279.
    • (2005) Pediatrics , vol.118 , pp. 276-279
    • Maisels, M.J.1    Kring, E.2
  • 9
    • 58149158216 scopus 로고    scopus 로고
    • Red cell membrane: Past, present, and future
    • Mohandas N, Gallagher PG: Red cell membrane: past, present, and future. Blood 2008; 112: 3939-3948.
    • (2008) Blood , vol.112 , pp. 3939-3948
    • Mohandas, N.1    Gallagher, P.G.2
  • 12
    • 64849110049 scopus 로고    scopus 로고
    • Hereditary stomatocytosis and cation-leaky red cells-recent developments
    • Bruce LJ: Hereditary stomatocytosis and cation-leaky red cells-recent developments. Blood Cells Mol Dis 2009; 42: 216-222.
    • (2009) Blood Cells Mol Dis , vol.42 , pp. 216-222
    • Bruce, L.J.1
  • 14
    • 56749112509 scopus 로고    scopus 로고
    • Can haptoglobin be an indicator for the early diagnosis of neonatal jaundice
    • Cakmak A, Calik M, Atas A, Hirfanoglu I, Erel O: Can haptoglobin be an indicator for the early diagnosis of neonatal jaundice J Clin Lab Anal 2008; 22: 409-414.
    • (2008) J Clin Lab Anal , vol.22 , pp. 409-414
    • Cakmak, A.1    Calik, M.2    Atas, A.3    Hirfanoglu, I.4    Erel, O.5
  • 16
    • 0036304975 scopus 로고    scopus 로고
    • Isoimmunization is unlikely to be the cause of hemolysis in ABO-incompatible but direct antiglobulin test-negative neonates
    • Herschel M, Karrison T, Wen M, Caldarelli L, Baron B: Isoimmunization is unlikely to be the cause of hemolysis in ABO-incompatible but direct antiglobulin test-negative neonates. Pediatrics 2002; 110: 127-130.
    • (2002) Pediatrics , vol.110 , pp. 127-130
    • Herschel, M.1    Karrison, T.2    Wen, M.3    Caldarelli, L.4    Baron, B.5
  • 18
    • 84877284044 scopus 로고    scopus 로고
    • A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: A rare case of autosomal-recessive hereditary spherocytosis due to -spectrin deficiency
    • Yaish HM, Christensen RD, Agarwal A: A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to -spectrin deficiency. J Perinatol 2013; 33: 404-406.
    • (2013) J Perinatol , vol.33 , pp. 404-406
    • Yaish, H.M.1    Christensen, R.D.2    Agarwal, A.3
  • 19
    • 0026354183 scopus 로고
    • Diagnostic utility of the pre-incubated acidified glycerol lysis test in haemolytic and non-haemolytic anaemias
    • Hoffmann JJ, Swaak-Lammers N, Breed WP, Strengers JL: Diagnostic utility of the pre-incubated acidified glycerol lysis test in haemolytic and non-haemolytic anaemias. Eur J Haematol 1991; 47: 367-370.
    • (1991) Eur J Haematol , vol.47 , pp. 367-370
    • Hoffmann, J.J.1    Swaak-Lammers, N.2    Breed, W.P.3    Strengers, J.L.4
  • 20
    • 77449109504 scopus 로고    scopus 로고
    • Evaluation of eosin-5-maleimide flow cytometric test in diagnosis of hereditary spherocytosis
    • Kar R, Mishra P, Pati HP: Evaluation of eosin-5-maleimide flow cytometric test in diagnosis of hereditary spherocytosis. Int J Lab Hematol 2010; 32: 8-16.
    • (2010) Int J Lab Hematol , vol.32 , pp. 8-16
    • Kar, R.1    Mishra, P.2    Pati, H.P.3
  • 21
    • 74049158630 scopus 로고    scopus 로고
    • Hereditary spherocytosis in neonates with hyperbilirubinemia
    • Christensen RD, Henry E: Hereditary spherocytosis in neonates with hyperbilirubinemia. Pediatrics 2010; 125: 120-125.
    • (2010) Pediatrics , vol.125 , pp. 120-125
    • Christensen, R.D.1    Henry, E.2
  • 22
    • 84876495957 scopus 로고    scopus 로고
    • Hereditary red cell membrane disorders and laboratory diagnostic testing
    • King MJ, Zanella A: Hereditary red cell membrane disorders and laboratory diagnostic testing. Int J Lab Hematol 2013; 35: 237-243.
    • (2013) Int J Lab Hematol , vol.35 , pp. 237-243
    • King, M.J.1    Zanella, A.2
  • 23
    • 84886739356 scopus 로고    scopus 로고
    • Variations in both -spectrin (SPTA1) and -spectrin (SPTB) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis
    • Christensen RD, Nussenzveig RH, Reading NS, Agarwal AM, Prchal JT, Yaish HM: Variations in both -spectrin (SPTA1) and -spectrin (SPTB) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis. Neonatology 2014; 105: 1-4.
    • (2014) Neonatology , vol.105 , pp. 1-4
    • Christensen, R.D.1    Nussenzveig, R.H.2    Reading, N.S.3    Agarwal, A.M.4    Prchal, J.T.5    Yaish, H.M.6
  • 24
    • 0026517040 scopus 로고
    • Drug-associated 'bite cell' hemolytic anemia
    • Yoo D, Lessin LS: Drug-associated 'bite cell' hemolytic anemia. Am J Med 1992; 92: 243-248.
    • (1992) Am J Med , vol.92 , pp. 243-248
    • Yoo, D.1    Lessin, L.S.2
  • 25
    • 0031867939 scopus 로고    scopus 로고
    • What's eating these red blood cells Drug-induced 'bite-cell' hemolytic anemia
    • Mishriki YY: What's eating these red blood cells Drug-induced 'bite-cell' hemolytic anemia. Postgrad Med 1998; 104: 45-46.
    • (1998) Postgrad Med , vol.104 , pp. 45-46
    • Mishriki, Y.Y.1
  • 26
    • 0021275753 scopus 로고
    • Molecular stability and function of hemoglobins Hasharon (2 47 (CD5)Asp-His- 2 ) and Hasharon (2 47 (CD5)Asp-His-2 )
    • Bender JW, Reilly MP, Asakura T: Molecular stability and function of hemoglobins Hasharon (2 47 (CD5)Asp-His- 2 ) and Hasharon (2 47 (CD5)Asp-His-2 ). Hemoglobin 1984; 8: 61-73.
    • (1984) Hemoglobin , vol.8 , pp. 61-73
    • Bender, J.W.1    Reilly, M.P.2    Asakura, T.3
  • 29
    • 80052815886 scopus 로고    scopus 로고
    • Six children with pyruvate kinase deficiency from one small town: Molecular characterization of the PK-LR gene
    • Christensen RD, Yaish HM, Johnson CB, Bianchi P, Zanella A: Six children with pyruvate kinase deficiency from one small town: molecular characterization of the PK-LR gene. J Pediatr 2011; 159: 695-697.
    • (2011) J Pediatr , vol.159 , pp. 695-697
    • Christensen, R.D.1    Yaish, H.M.2    Johnson, C.B.3    Bianchi, P.4    Zanella, A.5
  • 30
  • 31
    • 80053293826 scopus 로고    scopus 로고
    • Clinical use of fresh-frozen plasma and cryoprecipitate in neonatal intensive care unit
    • Motta M, Del Vecchio A, Radicioni M: Clinical use of fresh-frozen plasma and cryoprecipitate in neonatal intensive care unit. J Matern Fetal Neonatal Med 2011; 24(suppl 1): 129-131.
    • (2011) J Matern Fetal Neonatal Med , vol.24 , Issue.SUPPL. 1 , pp. 129-131
    • Motta, M.1    Del Vecchio, A.2    Radicioni, M.3
  • 32
    • 74049137935 scopus 로고    scopus 로고
    • ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura
    • Lotta LA, Garagiola I, Palla R, Cairo A, Peyvandi F: ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura. Hum Mutat 2010; 31: 11-19.
    • (2010) Hum Mutat , vol.31 , pp. 11-19
    • Lotta, L.A.1    Garagiola, I.2    Palla, R.3    Cairo, A.4    Peyvandi, F.5
  • 33
    • 3843152878 scopus 로고    scopus 로고
    • Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency
    • Schiff DE, Roberts WD, Willert J, Tsai HM: Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency. J Pediatr Hematol Oncol 2004; 26: 535-538.
    • (2004) J Pediatr Hematol Oncol , vol.26 , pp. 535-538
    • Schiff, D.E.1    Roberts, W.D.2    Willert, J.3    Tsai, H.M.4
  • 34
    • 84865795302 scopus 로고    scopus 로고
    • A phenotype-genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom
    • Camilleri RS, Scully M, Thomas M, Mackie IJ, Liesner R, Chen WJ, Manns K, Machin SJ: A phenotype-genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom. J Thromb Haemost 2012; 10: 1792-1801.
    • (2012) J Thromb Haemost , vol.10 , pp. 1792-1801
    • Camilleri, R.S.1    Scully, M.2    Thomas, M.3    Mackie, I.J.4    Liesner, R.5    Chen, W.J.6    Manns, K.7    Machin, S.J.8
  • 35
    • 1642496931 scopus 로고    scopus 로고
    • Diagnosis and treatment of a newborn with homozygous protein C deficiency
    • Salonvaara M, Kuismanen K, Mononen T, Riikonen P: Diagnosis and treatment of a newborn with homozygous protein C deficiency. Acta Paediatr 2004; 93: 137-139.
    • (2004) Acta Paediatr , vol.93 , pp. 137-139
    • Salonvaara, M.1    Kuismanen, K.2    Mononen, T.3    Riikonen, P.4
  • 36
    • 84868249189 scopus 로고    scopus 로고
    • Neonatal atypical hemolytic uremic syndrome may cause prenatal asphyxia
    • Fallahpour M, Hafizi A, Fouladgar A, Rajabian B: Neonatal atypical hemolytic uremic syndrome may cause prenatal asphyxia. Arch Iran Med 2012; 15: 729-730.
    • (2012) Arch Iran Med , vol.15 , pp. 729-730
    • Fallahpour, M.1    Hafizi, A.2    Fouladgar, A.3    Rajabian, B.4
  • 38
    • 84863980391 scopus 로고    scopus 로고
    • Neonatal atypical hemolytic uremic syndrome due to methylmalonic aciduria and homocystinuria
    • Menni F, Testa S, Guez S, Chiarelli G, Alberti L, Esposito S: Neonatal atypical hemolytic uremic syndrome due to methylmalonic aciduria and homocystinuria. Pediatr Nephrol 2012; 27: 1401-1405.
    • (2012) Pediatr Nephrol , vol.27 , pp. 1401-1405
    • Menni, F.1    Testa, S.2    Guez, S.3    Chiarelli, G.4    Alberti, L.5    Esposito, S.6
  • 39
    • 84883054621 scopus 로고    scopus 로고
    • Diagnosis of atypical hemolytic uremic syndrome: A review of case studies
    • Laurence J: Diagnosis of atypical hemolytic uremic syndrome: a review of case studies. Clin Adv Hematol Oncol 2012; 10(suppl 17): 9-11.
    • (2012) Clin Adv Hematol Oncol , vol.10 , Issue.SUPPL. 17 , pp. 9-11
    • Laurence, J.1
  • 40
    • 0025063158 scopus 로고
    • Neonatal hepatic haemangioendothelioma: Presentation with jaundice and microangiopathic haemolytic anaemia
    • Yohannan MD, Abdulla AM, Patel PJ: Neonatal hepatic haemangioendothelioma: presentation with jaundice and microangiopathic haemolytic anaemia. Eur J Pediatr 1990; 149: 804-805.
    • (1990) Eur J Pediatr , vol.149 , pp. 804-805
    • Yohannan, M.D.1    Abdulla, A.M.2    Patel, P.J.3
  • 42
    • 84902544469 scopus 로고    scopus 로고
    • Examination of the blood smear
    • Greer JP Foerster J Rodgers GM Paraskevas F Glader B Arber DA Means RT Jr (eds) ed 12. Philadelphia, Lippincott/Williams & Wilkins
    • Perkins SL: Examination of the blood smear; in Greer JP, Foerster J, Rodgers GM, Paraskevas F, Glader B, Arber DA, Means RT Jr (eds): Wintrobe's Clinical Hematology, ed 12. Philadelphia, Lippincott/Williams & Wilkins, 2009, pp 9-10.
    • (2009) Wintrobe's Clinical Hematology , pp. 9-10
    • Perkins, S.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.