Monosomy X as a recurring sole cytogenetic abnormality associated with myelodysplastic diseases

Cancer Genetics and Cytogenetics

Volumn 93, Issue 2, 1997, Pages 140-146

  Abruzzese, Elisabetta ^a   Rao, P Nagesh ^a   Slatkoff, Marc ^c   Cruz, Julia ^b   Powell, Bayard L ^b   Jackle, Bethy ^a   Pettenati, Mark J ^a,b  

^a Department of Pediatrics   (United States)

^b WAKE FOREST SCHOOL OF MEDICINE   (United States)

^c Lyndhurst Oncology   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; BONE MARROW CELL; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CYTOGENETICS; DISEASE ASSOCIATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MONOSOMY X; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

EID: 0030904019     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(97)83556-X     Document Type: Article

References (41)

1. Mitelman F (1991): Catalog of Chromosome Aberration in Cancer. Fourth Ed., John Wiley and Sons Publishing Co., New York.
2. United Kingdom Cancer Cytogenetics Group (1992): Primary, single, autosomal trisomies associated with haematological disorders. Leukemia Res 16:841-851.
3. Heim S and Mitelman F (1986): Numerical chromosome aberration in human neoplasia. Cancer Genet Cytogenet 22:99-108.
4. Holmes RI, Keating MJ, Cork A, Trujillo JM, McCredit KB, Freireich (1985): Loss of the Y chromosome in acute myelogenous leukemia: A report of 13 patients. Cancer Genet Cytogenet 17:169-278.
5. Jotterand-Bellomo M, Parlier V, Schmidy PH, Beris PH (1989): Cytogenetic analysis of 54 cases of myelodysplastic syndrome. Cancer Genet Cytogenet 45:157-172.
6. Stone JF, Sandberg AA (1995): Sex chromosome aneuploidy and aging. Mutation Res 338:107-113.
7. Sandberg AA (1983): The X chromosome in human neoplasia, including sex chromatin and congenital conditions with X-chromosome anomalies. Cytogenetics of the Mammalian X Chromosome, Part B: X chromosome anomalies and their clinical manifestations, pp. 459-498. Alan R. Liss, Inc., New York.
8. Prosch U, Stobbe H (1985): Cytogenetic findings in acute myelogenous leukemias (FAB M 1 to M 6). Folia Haematol Int Mag Klin Morphol Blutforsch. 112:481-494.
9. Abruzzese E, Buss D, Rainer R, Rao PN, Pettanati MJ (1996): Study of clonality in myelodysplastic syndromes: detection of trisomy 8 in bone marrow cells smears by fluorescence in situ hybridization. Leuk Res 20:551-557.
10. Gerritsen WR, Donohue J, Bauman J, Jhanwar SC, Kernan NA, Castro-Malaspina H, O'Reilly RJ, Bourhis J-H (1992): Clonal analysis of myelodysplastic syndrome: monosomy 7 is expressed in the myeloid lineage, but not in the lymphoid lineage as detected by fluorescent in situ hybridization. Blood 80:217-224.
11. Anastasi J, Feng J, LeBeau MM, Larson RA, Rowley JD, Vardiman JW (1993): Cytogenetic clonality in myelodysplastic syndromes studied with fluorescence in situ hybridization: Lineage, response to growth factor therapy, and clone expansion. Blood 81:1580-1588.
12. Abruzzese E, Buss D, Rainer R, Pettenati MJ, Rao PN (1996): Progression of a myelodysplastic syndrome to pre-B Acute lymphoblastic luekemia: a case report and cell lineage study. Ann Hematol 73:35-38.
13. Dewald GW, Pierre RV, Phyliky RL (1982): Three patients with structural abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia. Blood 59: 100-105.
14. Dewald GW, Brecher M, Travis LB, Stupca PJ (1989): Twenty-six patients with hematologic disorder and X chromosome abnormalities: Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts. Cancer Genet Cytogenet 42:173-185.
15. Petit P, Fryns JP, Masure R, Van Den Berghe H (1982): Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome? Cancer Genet Cytogenet 7:339-341.
16. Mackinnon WB, Michael PM, Webber LM, Garson OM (1988): Isodicentric X chromosomes involving the Xq13 breakpoint in myelodysplasia and acute nonlymphomatic leukemia. Cancer Genet Cytogenet 30:43-52
17. Temperani P, Zucchini P, Emilia G, Sacchi S, Selleri L, Torelli U (1989): Isodicentric X chromosome in myeloproliferative disorders. Acta Haematol 81:152-154.
18. Lewis FJW, Poulding RH, Eastham RD (1963): Acute leukaemia in an XO/XXX mosaic. Lancet 2:306.
19. Dumars KW, Kitzmiller N, Gaskill C (1967): Cancer, chromosomes and congenital abnormalities. Cancer 20:1006-1014.
20. Newman AJ, Gross S (1967): Turner's syndrome and congenital erythroid hyperplasia. Lancet 1:449.
21. Pawliger DF, Barrow M, Noyes WD (1970): Acute leukaemia and Turner's syndrome. Lancet 1:1345.
22. Wertelecki W, Fraumeni JF, Mulvihill JJ (1970): Nongonadal neoplasia in Turner's syndrome. Cancer 26:485-488.
23. Wertelecki W, Shapiro JR (1970): 45,XO Turner's syndrome and leukaemia. Lancet 1:789-790.
24. Julia A, Sanchez C, Tresanchez JM, Sarret E (1979): Leucemia mieloide cronica (Ph' positiva) en el sindrome de Turner (45,X0). Rev Clin Exp 153:399-402.
25. Chaganti RSK, Bailey RB, Jhanwar SC, Arllin ZA, Clarkson BD (1982): Chronic myelogenous leukemia in the monosomic cell line of a fertile Turner syndrome mosaic (45,X/46,XX). Cancer Genet Cytogenet 5:215-221.
26. Otokida K, Ohira K, Ishikawa M, Arakawa N, Yoshida A, Kamimura A, Kou E, Kato M (1990): A case of Turner syndrome with the karyotype of 45,X/46,X,i(Xq) associated with acute monocytic leukemia. Tohoku J Exp Med 161:19-24.
27. Itoh K, Igarashi T, Wakita H, Minamihisamatsu M (1992): Sideroblastic anemia associated with multiple myeloma in Turner's syndrome. Int Med 31:483-485.
28. Mitelman F, Nilsson PG, Brandt L, Alimena G, Gastaldi R and Dallapiccola B (1981): Chromosome pattern, occupation, and clinical features in patients with acute non-lymphocytic leukemia. Cancer Genet Cytogenet 4:197-214.
29. Alimena G (1983): Personal communication with F. Mitelman (1988).
30. Chrz R, Michalova J, Musilova J (1985) Personal communication with F. Mitelman (1988).
31. Riske CB, Morgan R, Ondreyco S, Sandberg AA (1994): X and Y chromosome loss as sole abnormality in acute non-lymphocytic leukemia (ANLL). Cancer Genet Cytogenet 72:44-47.
32. Appelbaum FR, Barrall J, Storb R, Ramberg R, Doney K, Sale GE and Thomas ED (1987): Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia. Exp Hematol 15:1134-1139.
33. Suciu S, Kuse R, Weh HJ, Hossfeld DK (1990): Results of chromosome studies and their relation to morphology, course, and prognosis in 120 patients with de novo myelodysplastic syndrome. Cancer Genet Cytogenet 44:15-26.
34. Yamada Y, Furusawa S (1976): Preferential involvement of chromosomes No. 8 and No. 21 in acute leukemia and preleukemia. Blood 47:679-686.
35. Heerema NA, Palmer CG, Baehner RL (1985): Karyotypic and clinical findings in a consecutive series of children with acute lymphocytic leukemia. Cancer Genet Cytogenet 17:165-179.
36. Prigonina EL, Puchkova GP, Mayakova SA (1988): Nonrandom chromosomal abnormalities in acute lymphoblastic leukemia of childhood. Cancer Genet Cytogenet 32:183-203.
37. Gallen DF, Ford JH (1983): Chromosome abnormalities in chronic lymphocytic leukemia revealed by TPA as a mitogen. Cancer Genet Cytogenet 10:87-93.
38. Bird ML, Ueshima Y, Rowley JD, Haren JM, Vardiman JW (1989): Chromosome abnormalities in B cell chronic lymphocytic leukemia and their clinical correlations. Leukemia 3:182-191.
39. Nordenson (1985): Personal communication with F. Mitelman 1988.
40. Lisse IM, Drivsholm A and Christoffersen P (1988): Occurrence and type of chromosomal abnormalities in consecutive malignant monoclonal gammopathies: Correlation with survival. Cancer Genet Cytogenet 35:27-36.
41. Taniwaki M, Nishida K, Misawa S, Takino T, Abe T, Aozasa K, Katagiri S, Uonezawa T, Matsuzuka F, Kuma K (1989): Correlation of chromosome abnormalities with clinical characteristics in thyroid lymphoma. Cancer 63:873-876.