Page 1093 - Hematology_ Basic Principles and Practice ( PDFDrive )
P. 1093

Chapter 60  Myelodysplastic Syndromes  969.e7


            277.  Pagliuca A, Layton DM, Manoharan A, et al: Myelofibrosis in primary   302.  Kornberg A, Goldfarb A: Preleukemia manifested by hemolytic anemia
                myelodysplastic syndromes: a clinico-morphological study of 10 cases.   with  pyruvate-kinase  deficiency.  Arch  Intern  Med  146(4):785–786,
                Br J Haematol 71(4):499–504, 1989.                    1986.
            278.  Nangalia  J,  Green  TR:  The  evolving  genomic  landscape  of  myelo-  303.  Hast R: Sideroblasts in myelodysplasia: their nature and clinical signifi-
                proliferative  neoplasms.  Hematology  Am  Soc  Hematol  Educ  Program   cance. Scand J Haematol Suppl 45:53–55, 1986.
                2014(1):287–296, 2014.                            304.  Steensma  DP,  Higgs  DR,  Fisher  CA,  et al:  Acquired  somatic  ATRX
            279.  Steensma DP, Heptinstall KV, Johnson VM, et al: Common trouble-  mutations in myelodysplastic syndrome associated with alpha thalas-
                some symptoms and their impact on quality of life in patients with   semia  (ATMDS)  convey  a  more  severe  hematologic  phenotype  than
                myelodysplastic  syndromes  (MDS):  results  of  a  large  internet-based   germline ATRX mutations. Blood 103(6):2019–2026, 2004.
                survey. Leuk Res 32(5):691–698, 2008.             305.  Annino L, Di Giovanni S, Tentorì L, et al: Acquired hemoglobin H
            280.  Pomeroy C, Oken MM, Rydell RE, et al: Infection in the myelodys-  disease in a case of refractory anemia with excess of blasts (RAEB) evolv-
                plastic syndromes. Am J Med 90(3):338–344, 1991.      ing  into  acute  nonlymphoid  leukemia.  Acta  Haematol  72(1):41–44,
            281.  Raman B, Van Slyck E, Riddle J, et al: Platelet function and structure   1984.
                in myeloproliferative disease, myelodysplastic syndrome, and secondary   306.  French Registry of Acute Leukemia and Myelodysplastic Syndromes:
                thrombocytosis. Am J Clin Pathol 647:91, 1989.        Age  distribution  and  hemogram  analysis  of  the  4496  cases  recorded
            282.  Avivi I, Rosenbaum H, Levy Y, et al: Myelodysplastic syndrome and   during  and  classified  according  to  criteria  FAB,  Groupe  Francais  de
                associated skin lesions: a review of the literature. Leuk Res 23(4):323–  Morphologie Hematologique. Cancer 60:1982–1983, 1987. 1385.
                330, 1999.                                        307.  Cech P, Markert M, Perrin LH: Partial myeloperoxidase deficiency in
            283.  Rochet NM, Chavan RN, Cappel MA, et al: Sweet syndrome: clinical   preleukemia. Blut 47(1):21–30, 1983.
                presentation,  associations,  and  response  to  treatment  in  77  patients.    308.  Prodan M, Tulissi P, Perticarari S, et al: Flow cytometric assay for the
                J Am Acad Dermatol 69(4):557–564, 2013.               evaluation of phagocytosis and oxidative burst of polymorphonuclear
            284.  Ten Oever J, Kuijper PHM, Kuijpers ALA, et al: Complete remission   leukocytes and monocytes in myelodysplastic disorders. Haematologica
                of MDS RAEB following immunosuppressive treatment in a patient   80(3):212–218, 1995.
                with Sweet’s syndrome. Neth J Med 67(8):347–350, 2009.  309.  Ruutu P: Granulocyte function in myelodysplastic syndromes. Scand J
            285.  Jo T, Horio K, Migita K: Sweet’s syndrome in patients with MDS and   Haematol Suppl 45:66–70, 1986.
                MEFV mutations. N Engl J Med 372(7):686–688, 2015.  310.  Schanz  J, Tüchler  H,  Solé  F,  et al:  New  comprehensive  cytogenetic
            286.  Srivastava  M,  Rencic  A,  Nousari  HC:  A  rapidly  expanding  ulcer.   scoring  system  for  primary  myelodysplastic  syndromes  (MDS)  and
                Myelodysplastic  syndrome-associated  (paraneoplastic)  pyoderma  gan-  oligoblastic acute myeloid leukemia after MDS derived from an inter-
                grenosum. Arch Dermatol 139(4):531–536, 2003.         national database merge. J Clin Oncol 30(8):820–829, 2012.
            287.  Duguid JK, Mackie MJ, McVerry BA: Skin infiltration associated with   311.  Tricot G, De Wolf-Peeters C, Vlietinck R, et al: Bone marrow histology
                chronic  myelomonocytic  leukaemia.  Br  J  Haematol  53(2):257–264,   in myelodysplastic syndromes. II. Prognostic value of abnormal localiza-
                1983.                                                 tion of immature precursors in MDS. Br J Haematol 58(2):217–225,
            288.  Enright  H,  Miller  W:  Autoimmune  phenomena  in  patients  with   1984.
                myelodysplastic syndromes. Leuk Lymphoma 24(5–6):483–489, 1997.  312.  Della  Porta  MG,  Malcovati  L,  Boveri  E,  et al:  Clinical  relevance  of
            289.  George  S,  Newman  E:  Seronegative  inflammatory  arthritis  in  the   bone  marrow  fibrosis  and  CD34-positive  cell  clusters  in  primary
                myelodysplastic  syndromes.  Semin  Arthritis  Rheum  21:345–354,   myelodysplastic syndromes. J Clin Oncol 27(5):754–762, 2009.
                1992.                                             313.  Williamson PJ, Oscier DG, Mufti GJ, et al: Pyogenic abscesses in the
            290.  Green  AR,  Shuttleworth  D,  Bowen  DT,  et al:  Cutaneous  vasculitis     myelodysplastic syndrome. BMJ 299(6695):375–376, 1989.
                in  patients  with  myelodysplasia.  Br  J  Haematol  74(3):364–365,   314.  Rasi V, Lintula R: Platelet function in the myelodysplastic syndromes.
                1990.                                                 Scand J Haematol Suppl 45:71–73, 1986.
            291.  Tsuji  G,  Maekawa  S,  Saigo  K,  et al:  Dermatomyositis  and  myelo-  315.  Girtovitis FI, Ntaios G, Papadopoulos A, et al: Defective platelet aggre-
                dysplastic  syndrome  with  myelofibrosis  responding  to  methotrexate   gation in myelodysplastic syndromes. Acta Haematol 118(2):117–122,
                therapy. Am J Hematol 74(3):175–178, 2003.            2007.
            292.  Enright H, Jacob HS, Vercellotti G, et al: Paraneoplastic autoimmune   316.  Zeidman  A,  Sokolover  N,  Fradin  Z,  et al:  Platelet  function  and  its
                phenomena  in  patients  with  myelodysplastic  syndromes:  response  to   clinical  significance  in  the  myelodysplastic  syndromes.  Hematol  J
                immunosuppressive therapy. Br J Haematol 91(2):403–408, 1995.  5(3):234–238, 2004.
            293.  Heo S-W, Cho K-H, Ryu J-I, et al: A case of relapsing polychondritis   317.  Szpurka H, Tiu R, Murugesan G, et al: Refractory anemia with ringed
                associated with myelodysplastic syndrome with erythroid hypoplasia/  sideroblasts associated with marked thrombocytosis (RARS-T), another
                aplasia. Korean J Intern Med 18(4):251–254, 2003.     myeloproliferative condition characterized by JAK2 V617F mutation.
            294.  Steurer  M,  Fritsche  G,  Tzankov  A,  et al:  Large-vessel  arteritis  and   Blood 108(7):2173–2181, 2006.
                myelodysplastic  syndrome:  report  of  two  cases.  Eur  J  Haematol   318.  Kuriyama K, Tomonaga M, Matsuo T, et al: Diagnostic significance of
                73(2):128–133, 2004.                                  detecting pseudo-Pelger-Huët anomalies and micro-megakaryocytes in
            295.  Saitoh T, Murakami H, Uchiumi H, et al: Myelodysplastic syndromes   myelodysplastic syndrome. Br J Haematol 63(4):665–669, 1986.
                with nephrotic syndrome. Am J Hematol 60(3):200–204, 1999.  319.  Queisser  W,  Queisser  U,  Ansmann  M,  et al:  Megakaryocyte  poly-
            296.  Linman  JW,  Bagby  GC:  The  preleukemic  syndrome  (hemopoietic   ploidization  in  acute  leukaemia  and  preleukaemia.  Br  J  Haematol
                dysplasia). Cancer 42(2 Suppl):854–864, 1978.         28(2):261–270, 1974.
            297.  Noel P, Solberg L, Jr: Myelodysplastic syndromes. Pathog Diagn Treat   320.  Takagi S, Kitagawa S, Takeda A, et al: Natural killer-interferon system
                Crit Rev Oncol 12(3):193–215, 1992.                   in patients with preleukaemic states. Br J Haematol 58(1):71–81, 1984.
            298.  Bowen DT, Jacobs A, Cotes PM, et al: Serum erythropoietin and eryth-  321.  Kerndrup G, Meyer K, Ellegaard J, et al: Natural killer (NK)-cell activ-
                ropoiesis in patients with myelodysplastic syndromes. Eur J Haematol   ity and antibody-dependent cellular cytotoxicity (ADCC) in primary
                44(1):30–32, 1990.                                    preleukemic syndrome. Leuk Res 8(2):239–247, 1984.
            299.  Kushner J, Porter J, Olivieri N: Secondary iron overload. Hematology   322.  Britanova OV, Putintseva EV, Shugay M, et al: Age-related decrease in
                Am Soc Hematol Educ Program 47, 2001.                 TCR repertoire diversity measured with deep and normalized sequence
            300.  Choi JW, Kim Y, Fujino M, et al: Significance of fetal hemoglobin-  profiling. J Immunol 1950 192(6):2689–2698, 2014.
                containing  erythroblasts  (F  blasts)  and  the  F  blast/F  cell  ratio  in   323.  Gibson KL, Wu Y-C, Barnett Y, et al: B-cell diversity decreases in old
                myelodysplastic syndromes. Leukemia 16(8):1478–1483, 2002.  age and is correlated with poor health status. Aging Cell 8(1):18–25,
            301.  Lopez  M,  Bonnet-Gajdos  M,  Reviron  M,  et al:  An  acute  leukaemia   2009.
                augured before clinical signs by blood group antigen abnormalities and   324.  Wells RA, Leber B, Buckstein R, et al: Iron overload in myelodysplastic
                low levels of A and H blood group transferase activities in erythrocytes.   syndromes: a Canadian consensus guideline. Leuk Res 32(9):1338–1353,
                Br J Haematol 63(3):535–539, 1986.                    2008.
   1088   1089   1090   1091   1092   1093   1094   1095   1096   1097   1098