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Volumn 21, Issue 5, 2013, Pages 520-525

Posttransplant lymphoproliferative disorder complicating hematopoietic stem cell transplantation in a patient with dyskeratosis congenita

Author keywords

acute myeloid leukemia; aplastic anemia; dyskeratosis congenita; posttransplant lymphoproliferative disorder

Indexed keywords

BUSULFAN; CYCLOPHOSPHAMIDE; FLUDARABINE; GRANULOCYTE COLONY STIMULATING FACTOR; RITUXIMAB; THYMOCYTE ANTIBODY;

EID: 84884696785     PISSN: 10668969     EISSN: 19402465     Source Type: Journal    
DOI: 10.1177/1066896912468214     Document Type: Article
Times cited : (9)

References (28)
  • 1
    • 84855486059 scopus 로고    scopus 로고
    • Dyskeratosis congenita as a disorder of telomere maintenance
    • Nelson ND, Bertuch AA. Dyskeratosis congenita as a disorder of telomere maintenance. Mutat Res. 2012 ; 730: 43-51
    • (2012) Mutat Res , vol.730 , pp. 43-51
    • Nelson, N.D.1    Bertuch, A.A.2
  • 3
    • 84855490226 scopus 로고    scopus 로고
    • Maintaining the end: Roles of telomere proteins in end-protection, telomere replication and length regulation
    • Stewart JA, Chaiken MF, Wang F, Price CM. Maintaining the end: roles of telomere proteins in end-protection, telomere replication and length regulation. Mutat Res. 2012 ; 730: 12-19
    • (2012) Mutat Res , vol.730 , pp. 12-19
    • Stewart, J.A.1    Chaiken, M.F.2    Wang, F.3    Price, C.M.4
  • 4
    • 34547410832 scopus 로고    scopus 로고
    • Dyskeratosis congenita: Advances in the understanding of the telomerase defect and the role of stem cell transplantation
    • de la Fuente J, Dokal I. Dyskeratosis congenita: advances in the understanding of the telomerase defect and the role of stem cell transplantation. Pediatr Transplant. 2007 ; 11: 584-594
    • (2007) Pediatr Transplant , vol.11 , pp. 584-594
    • De La Fuente, J.1    Dokal, I.2
  • 6
    • 0026803181 scopus 로고
    • Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: A new syndrome?
    • Revesz T, Fletcher S, al-Gazali LI, DeBuse P. Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?. J Med Genet. 1992 ; 29: 673-675
    • (1992) J Med Genet , vol.29 , pp. 673-675
    • Revesz, T.1    Fletcher, S.2    Al-Gazali, L.I.3    Debuse, P.4
  • 7
    • 0023731072 scopus 로고
    • A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure
    • Hreidarsson S, Kristjansson K, Johannesson G, Johannsson JH. A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure. Acta Paediatr Scand. 1988 ; 77: 773-775
    • (1988) Acta Paediatr Scand , vol.77 , pp. 773-775
    • Hreidarsson, S.1    Kristjansson, K.2    Johannesson, G.3    Johannsson, J.H.4
  • 8
    • 34247188473 scopus 로고    scopus 로고
    • Telomere and telomerase in stem cells
    • Hiyama E, Hiyama K. Telomere and telomerase in stem cells. Br J Cancer. 2007 ; 96: 1020-1024
    • (2007) Br J Cancer , vol.96 , pp. 1020-1024
    • Hiyama, E.1    Hiyama, K.2
  • 9
    • 46249125488 scopus 로고    scopus 로고
    • How shelterin protects mammalian telomeres
    • Palm W, de Lange T. How shelterin protects mammalian telomeres. Annu Rev Genet. 2008 ; 42: 301-334
    • (2008) Annu Rev Genet , vol.42 , pp. 301-334
    • Palm, W.1    De Lange, T.2
  • 11
    • 0035960043 scopus 로고    scopus 로고
    • The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
    • Vulliamy T, Marrone A, Goldman F, et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature. 2001 ; 413: 432-435
    • (2001) Nature , vol.413 , pp. 432-435
    • Vulliamy, T.1    Marrone, A.2    Goldman, F.3
  • 12
    • 18844421369 scopus 로고    scopus 로고
    • Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure
    • Vulliamy TJ, Walne A, Baskaradas A, Mason PJ, Marrone A, Dokal I. Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure. Blood Cells Mol Dis. 2005 ; 34: 257-263
    • (2005) Blood Cells Mol Dis , vol.34 , pp. 257-263
    • Vulliamy, T.J.1    Walne, A.2    Baskaradas, A.3    Mason, P.J.4    Marrone, A.5    Dokal, I.6
  • 13
    • 34447307404 scopus 로고    scopus 로고
    • Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10
    • Walne AJ, Vulliamy T, Marrone A, et al. Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10. Hum Mol Genet. 2007 ; 16: 1619-1629
    • (2007) Hum Mol Genet , vol.16 , pp. 1619-1629
    • Walne, A.J.1    Vulliamy, T.2    Marrone, A.3
  • 14
    • 45849131292 scopus 로고    scopus 로고
    • Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita
    • Vulliamy T, Beswick R, Kirwan M, et al. Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita. Proc Natl Acad Sci U S A. 2008 ; 105: 8073-8078
    • (2008) Proc Natl Acad Sci U S A , vol.105 , pp. 8073-8078
    • Vulliamy, T.1    Beswick, R.2    Kirwan, M.3
  • 15
    • 40749085700 scopus 로고    scopus 로고
    • TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita
    • Savage SA, Giri N, Baerlocher GM, Orr N, Lansdorp PM, Alter BP. TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita. Am J Hum Genet. 2008 ; 82: 501-509
    • (2008) Am J Hum Genet , vol.82 , pp. 501-509
    • Savage, S.A.1    Giri, N.2    Baerlocher, G.M.3    Orr, N.4    Lansdorp, P.M.5    Alter, B.P.6
  • 16
    • 66549099010 scopus 로고    scopus 로고
    • Risk factors for lymphoproliferative disorders after allogeneic hematopoietic cell transplantation
    • Landgren O, Gilbert ES, Rizzo JD, et al. Risk factors for lymphoproliferative disorders after allogeneic hematopoietic cell transplantation. Blood. 2009 ; 113: 4992-5001
    • (2009) Blood , vol.113 , pp. 4992-5001
    • Landgren, O.1    Gilbert, E.S.2    Rizzo, J.D.3
  • 17
    • 0029031757 scopus 로고
    • Posttransplantation lymphoproliferative disorders in solid organ recipients are predominantly aggressive tumors of host origin
    • Weissmann DJ, Ferry JA, Harris NL, Louis DN, Delmonico F, Spiro I. Posttransplantation lymphoproliferative disorders in solid organ recipients are predominantly aggressive tumors of host origin. Am J Clin Pathol. 1995 ; 103: 748-755
    • (1995) Am J Clin Pathol , vol.103 , pp. 748-755
    • Weissmann, D.J.1    Ferry, J.A.2    Harris, N.L.3    Louis, D.N.4    Delmonico, F.5    Spiro, I.6
  • 18
    • 33746930872 scopus 로고    scopus 로고
    • Posttransplant lymphoproliferative disorder in a kidney-pancreas transplanted recipient: Simultaneous development of clonal lymphoid B-cell proliferation of host and donor origin
    • Heyny-von Haussen R, Klingel K, Riegel W, Kandolf R, Mall G. Posttransplant lymphoproliferative disorder in a kidney-pancreas transplanted recipient: simultaneous development of clonal lymphoid B-cell proliferation of host and donor origin. Am J Surg Pathol. 2006 ; 30: 900-905
    • (2006) Am J Surg Pathol , vol.30 , pp. 900-905
    • Heyny-Von Haussen, R.1    Klingel, K.2    Riegel, W.3    Kandolf, R.4    Mall, G.5
  • 19
    • 79958786439 scopus 로고    scopus 로고
    • Post-transplant lymphoproliferative disorders: Determination of donor/recipient origin in a large cohort of kidney recipients
    • Olagne J, Caillard S, Gaub MP, Chenard MP, Moulin B. Post-transplant lymphoproliferative disorders: determination of donor/recipient origin in a large cohort of kidney recipients. Am J Transplant. 2011 ; 11: 1260-1269
    • (2011) Am J Transplant , vol.11 , pp. 1260-1269
    • Olagne, J.1    Caillard, S.2    Gaub, M.P.3    Chenard, M.P.4    Moulin, B.5
  • 20
    • 70349688283 scopus 로고    scopus 로고
    • 4th ed.Lyon, France: International Agency for Research on Cancer; 2008:343-349. Swerdlow SH Campo E Harris NL, ed. Lyon, France: International Agency for Research on Cancer;
    • Swerlow SH, Webber SA, Chadburn A, Ferry JA WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4 th ed.Lyon, France: International Agency for Research on Cancer; 2008:343-349. Swerdlow SH Campo E Harris NL, ed. Lyon, France: International Agency for Research on Cancer ; 2008: 343-349.
    • (2008) WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues , pp. 343-349
    • Swerlow, S.H.1    Webber, S.A.2    Chadburn, A.3    Ferry, J.A.4
  • 22
    • 0035016682 scopus 로고    scopus 로고
    • Post renal transplantation human herpesvirus 8-associated lymphoproliferative disorder and Kaposi's sarcoma
    • Kapelushnik J, Ariad S, Benharroch D, et al. Post renal transplantation human herpesvirus 8-associated lymphoproliferative disorder and Kaposi's sarcoma. Br J Haematol. 2001 ; 113: 425-428
    • (2001) Br J Haematol , vol.113 , pp. 425-428
    • Kapelushnik, J.1    Ariad, S.2    Benharroch, D.3
  • 23
    • 0141544900 scopus 로고    scopus 로고
    • Is posttransplant lymphoproliferative disorder (PTLD) caused by any specific immunosuppressive drug or by the transplantation per se?
    • Birkeland SA, Hamilton-Dutoit S. Is posttransplant lymphoproliferative disorder (PTLD) caused by any specific immunosuppressive drug or by the transplantation per se?. Transplantation. 2003 ; 76: 984-988
    • (2003) Transplantation , vol.76 , pp. 984-988
    • Birkeland, S.A.1    Hamilton-Dutoit, S.2
  • 24
    • 34548251516 scopus 로고    scopus 로고
    • Gene expression profiling of Epstein-Barr virus-positive and -negative monomorphic B-cell posttransplant lymphoproliferative disorders
    • Craig FE, Johnson LR, Harvey SA, et al. Gene expression profiling of Epstein-Barr virus-positive and -negative monomorphic B-cell posttransplant lymphoproliferative disorders. Diagn Mol Pathol. 2007 ; 16: 158-168
    • (2007) Diagn Mol Pathol , vol.16 , pp. 158-168
    • Craig, F.E.1    Johnson, L.R.2    Harvey, S.A.3
  • 25
    • 81855201855 scopus 로고    scopus 로고
    • Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory
    • De Braekeleer E, Meyer C, Douet-Guilbert N, et al. Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory. Mol Oncol. 2011 ; 5: 555-563
    • (2011) Mol Oncol , vol.5 , pp. 555-563
    • De Braekeleer, E.1    Meyer, C.2    Douet-Guilbert, N.3
  • 26
    • 33846192859 scopus 로고    scopus 로고
    • Cytogenetic analysis of B-cell posttransplant lymphoproliferations validates the World Health Organization classification and suggests inclusion of florid follicular hyperplasia as a precursor lesion
    • Vakiani E, Nandula SV, Subramaniyam S, et al. Cytogenetic analysis of B-cell posttransplant lymphoproliferations validates the World Health Organization classification and suggests inclusion of florid follicular hyperplasia as a precursor lesion. Hum Pathol. 2007 ; 38: 315-325
    • (2007) Hum Pathol , vol.38 , pp. 315-325
    • Vakiani, E.1    Nandula, S.V.2    Subramaniyam, S.3
  • 27
    • 32544436112 scopus 로고    scopus 로고
    • Post-transplant lymphoproliferative disorder subtypes correlate with different recurring chromosomal abnormalities
    • Djokic M, Le Beau MM, Swinnen LJ, et al. Post-transplant lymphoproliferative disorder subtypes correlate with different recurring chromosomal abnormalities. Genes Chromosomes Cancer. 2006 ; 45: 313-318
    • (2006) Genes Chromosomes Cancer , vol.45 , pp. 313-318
    • Djokic, M.1    Le Beau, M.M.2    Swinnen, L.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.