Çocukluk Çağında Nötropeniye Yaklaşım

Ömer Devecioğlu; Sevinç Gümüş

doi:10.5222/j.child.2012.053

Çocukluk Çağında Nötropeniye Yaklaşım

Yıl 2012, Cilt: 12 Sayı: 2, 53 - 59, 01.04.2012

Ömer Devecioğlu Sevinç Gümüş

https://doi.org/10.5222/j.child.2012.053

https://izlik.org/JA85NF64GW

Öz

Nötropeni, çocukluk çağlarında çok önemli hematolojik sorunlardan biridir. Konjenital ve edinsel nedenlerle mey- dana gelebilir. Nötrofil sayısının çok düştüğü durumlarda

Anahtar Kelimeler

Nötropeni , ağır konjenital nötropeni , siklik nötropeni

Kaynakça

1. Fioredda F, Calvillo M, Bonanomi S, et al. Congenital and acquired neutropenia consensus on diagnosis from the Neutropenia Commitee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica). Pediatr Blood Cancer 2011;57(1):10-7. http://dx.doi.org/10.1002/pbc.23108 PMid:21448998
2. Bonilla MA. Disorders of white blood cells. In Manual of Pediatric Hematology and Oncology, Lanzkowsky ed, 5th edition, Amsterdam, Elsevier, 2011, pp:272-320.
3. Dale DC, Person RE, Bolyard AA, et al. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 2000;96:2317-22. PMid:11001877
4. Donadieu J, Fenneteau O, Beaupain B, et al. Congenital neutropenia: diagnosis, molecular bases and patient management. Orphanet J Rare Dis 2011;6:26 Review. PMid:21595885 PMCid:3127744
5. Dinauer MC and Newburger PE. Quantitative granulocyte and mononuclear phagocyte disorders. In Nathan and Oski’s Hematology of Infancy and Chilhood, Orkin SH, Nathan DG, Ginsburg D, Look AT, Fisher DE, Lux SE eds, 7th edition, Philadelphia, Saunders Elsevier, 2009, pp:1137-52.
6. Boxer LA and Newburger PE. A molecular classification of congenital neutropenia syndromes. Pediatr Blood Cancer 2007;49:609-14. http://dx.doi.org/10.1002/pbc.21282 PMid:17584878
7. Berliner N, Horwitz M, Loughran TP. Congenital and acquired neutropenia. Hematoogy Am Soc Educ Program 2004. pp:63-79. PMid:15561677
8. Vandenberghe P, Beel C. Severe congenital neutropenia,a genetically heterogeneous disease group with an increased risk of AML/MDS. Pediatr Rep 2011;3(Suppl 2):e9. PMid:22053285 PMCid:3206537 http://dx.doi.org/10.4081/pr.2011.s2.e9
9. Kostmann R. Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria. Acta Paediatr Suppl 1956;45:1-78. PMid:13326376
10. Ward AC, van Aesch YM, Gits J, et al. Novel point mutation in the extracellular domain of the granulocyte colonystimulating factor (G-CSF) receptor in a case of severe congenital neutropenia hyporesponsive to G-CSF treatment. J Exp Med 1999;190:497-507. PMid:10449521 PMCid:2195597 http://dx.doi.org/10.1084/jem.190.4.497
11. Freeman MH, Bonilla, Frier C, et al. Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy. Blood 2000; 96:429-36. PMid:10887102 http://dx.doi.org/10.1186/1750-1172-6-26
12. Menasche G, Ho CH, Sanal O, et al. Griscelli syndrome restricted to hypopigmentation results a melanophillin defect (GS3) or a MYO5A F-exon deletion. J Clin Invest 2003;112 (3):450-6. PMid:12897212 PMCid:166299
13. Bohn G, Allroth A, Brandes G, et al. A novel human primary immonodeficiencıency syndrome caused by deficiency of the endosomal adaptor protein. Nature Medicine 2007;13:1:39- 45. PMid:17195838 http://dx.doi.org/10.1038/nm1528
14. Bux J, Behrens G, Jaeger G,Welte K. Diagnosis and clinical course of autoimmune neutropenia in infancy: analysis of 240 cases. Blood 1998;91(1):181-6. PMid:9414283
15. Newburger PE, Boxer LA. Leukopenia. In Nelson Textbook of Pediatrics, Kliegman RM, Stanton BF, St.Geme III JW, Schor NF, Behrman RE eds, 19th edition, Philadelphia, Elsevier Saunders, 2009, pp:746-52.

Approach to Childhood Neutropenia

Yıl 2012, Cilt: 12 Sayı: 2, 53 - 59, 01.04.2012

Ömer Devecioğlu Sevinç Gümüş

https://doi.org/10.5222/j.child.2012.053

https://izlik.org/JA85NF64GW

Öz

Neutropenia is one of the most serious hematological prob- lems in childhood. Neutropenia, either acquired or conge- nital, is a decrease in neutrophil count

Anahtar Kelimeler

Neutropenia , severe konjenital neutropenia , cyclic neutropenia

Kaynakça

1. Fioredda F, Calvillo M, Bonanomi S, et al. Congenital and acquired neutropenia consensus on diagnosis from the Neutropenia Commitee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica). Pediatr Blood Cancer 2011;57(1):10-7. http://dx.doi.org/10.1002/pbc.23108 PMid:21448998
2. Bonilla MA. Disorders of white blood cells. In Manual of Pediatric Hematology and Oncology, Lanzkowsky ed, 5th edition, Amsterdam, Elsevier, 2011, pp:272-320.
3. Dale DC, Person RE, Bolyard AA, et al. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 2000;96:2317-22. PMid:11001877
4. Donadieu J, Fenneteau O, Beaupain B, et al. Congenital neutropenia: diagnosis, molecular bases and patient management. Orphanet J Rare Dis 2011;6:26 Review. PMid:21595885 PMCid:3127744
5. Dinauer MC and Newburger PE. Quantitative granulocyte and mononuclear phagocyte disorders. In Nathan and Oski’s Hematology of Infancy and Chilhood, Orkin SH, Nathan DG, Ginsburg D, Look AT, Fisher DE, Lux SE eds, 7th edition, Philadelphia, Saunders Elsevier, 2009, pp:1137-52.
6. Boxer LA and Newburger PE. A molecular classification of congenital neutropenia syndromes. Pediatr Blood Cancer 2007;49:609-14. http://dx.doi.org/10.1002/pbc.21282 PMid:17584878
7. Berliner N, Horwitz M, Loughran TP. Congenital and acquired neutropenia. Hematoogy Am Soc Educ Program 2004. pp:63-79. PMid:15561677
8. Vandenberghe P, Beel C. Severe congenital neutropenia,a genetically heterogeneous disease group with an increased risk of AML/MDS. Pediatr Rep 2011;3(Suppl 2):e9. PMid:22053285 PMCid:3206537 http://dx.doi.org/10.4081/pr.2011.s2.e9
9. Kostmann R. Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria. Acta Paediatr Suppl 1956;45:1-78. PMid:13326376
10. Ward AC, van Aesch YM, Gits J, et al. Novel point mutation in the extracellular domain of the granulocyte colonystimulating factor (G-CSF) receptor in a case of severe congenital neutropenia hyporesponsive to G-CSF treatment. J Exp Med 1999;190:497-507. PMid:10449521 PMCid:2195597 http://dx.doi.org/10.1084/jem.190.4.497
11. Freeman MH, Bonilla, Frier C, et al. Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy. Blood 2000; 96:429-36. PMid:10887102 http://dx.doi.org/10.1186/1750-1172-6-26
12. Menasche G, Ho CH, Sanal O, et al. Griscelli syndrome restricted to hypopigmentation results a melanophillin defect (GS3) or a MYO5A F-exon deletion. J Clin Invest 2003;112 (3):450-6. PMid:12897212 PMCid:166299
13. Bohn G, Allroth A, Brandes G, et al. A novel human primary immonodeficiencıency syndrome caused by deficiency of the endosomal adaptor protein. Nature Medicine 2007;13:1:39- 45. PMid:17195838 http://dx.doi.org/10.1038/nm1528
14. Bux J, Behrens G, Jaeger G,Welte K. Diagnosis and clinical course of autoimmune neutropenia in infancy: analysis of 240 cases. Blood 1998;91(1):181-6. PMid:9414283
15. Newburger PE, Boxer LA. Leukopenia. In Nelson Textbook of Pediatrics, Kliegman RM, Stanton BF, St.Geme III JW, Schor NF, Behrman RE eds, 19th edition, Philadelphia, Elsevier Saunders, 2009, pp:746-52.

Toplam 15 adet kaynakça vardır.

Ayrıntılar

Birincil Dil	Türkçe
Yazarlar	Ömer Devecioğlu Bu kişi benim Sevinç Gümüş Bu kişi benim
Yayımlanma Tarihi	1 Nisan 2012
DOI	https://doi.org/10.5222/j.child.2012.053
IZ	https://izlik.org/JA85NF64GW
Yayımlandığı Sayı	Yıl 2012 Cilt: 12 Sayı: 2

Kaynak Göster

APA	Devecioğlu, Ö., & Gümüş, S. (2012). Çocukluk Çağında Nötropeniye Yaklaşım. Çocuk Dergisi, 12(2), 53-59. https://doi.org/10.5222/j.child.2012.053
AMA	1.Devecioğlu Ö, Gümüş S. Çocukluk Çağında Nötropeniye Yaklaşım. Çocuk Dergisi. 2012;12(2):53-59. doi:10.5222/j.child.2012.053
Chicago	Devecioğlu, Ömer, ve Sevinç Gümüş. 2012. “Çocukluk Çağında Nötropeniye Yaklaşım”. Çocuk Dergisi 12 (2): 53-59. https://doi.org/10.5222/j.child.2012.053.
EndNote	Devecioğlu Ö, Gümüş S (01 Nisan 2012) Çocukluk Çağında Nötropeniye Yaklaşım. Çocuk Dergisi 12 2 53–59.
IEEE	[1]Ö. Devecioğlu ve S. Gümüş, “Çocukluk Çağında Nötropeniye Yaklaşım”, Çocuk Dergisi, c. 12, sy 2, ss. 53–59, Nis. 2012, doi: 10.5222/j.child.2012.053.
ISNAD	Devecioğlu, Ömer - Gümüş, Sevinç. “Çocukluk Çağında Nötropeniye Yaklaşım”. Çocuk Dergisi 12/2 (01 Nisan 2012): 53-59. https://doi.org/10.5222/j.child.2012.053.
JAMA	1.Devecioğlu Ö, Gümüş S. Çocukluk Çağında Nötropeniye Yaklaşım. Çocuk Dergisi. 2012;12:53–59.
MLA	Devecioğlu, Ömer, ve Sevinç Gümüş. “Çocukluk Çağında Nötropeniye Yaklaşım”. Çocuk Dergisi, c. 12, sy 2, Nisan 2012, ss. 53-59, doi:10.5222/j.child.2012.053.
Vancouver	1.Ömer Devecioğlu, Sevinç Gümüş. Çocukluk Çağında Nötropeniye Yaklaşım. Çocuk Dergisi. 01 Nisan 2012;12(2):53-9. doi:10.5222/j.child.2012.053