Hepatosplenic T-cell lymphoma with isochromosome 7q, translocation t(7;21), and tetrasomy 8 in a 9-year-old girl

American Journal of Pediatric Hematology/Oncology

Volumn 24, Issue 2, 2002, Pages 154-157

  Rossbach, Hans Christoph ^a   Chamizo, Wilfredo ^a   Dumont, Doris P ^a   Barbosa, Jerry L ^a   Sutcliffe, Maxine J ^a  

^a UNIVERSITY OF SOUTH FLORIDA   (United States)

Author keywords

Hepatosplenic T cell lymphoma; Isochromosome 7q; Tetrasomy 8; Translocation t(7,21)

Indexed keywords

CD16 ANTIGEN; CD3 ANTIGEN; CD56 ANTIGEN; T LYMPHOCYTE RECEPTOR;

ANTIGEN EXPRESSION; ARTICLE; BONE MARROW; CASE REPORT; CHROMOSOME 7Q; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; FEMALE; HEPATOSPLENOMEGALY; HUMAN; ISOCHROMOSOME; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; T CELL LYMPHOMA; TETRASOMY; THROMBOCYTOPENIA; TRISOMY 8;

ANEUPLOIDY; ANTIGENS, CD3; ANTIGENS, CD56; ANTIGENS, NEOPLASM; ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS; BONE MARROW; BONE MARROW TRANSPLANTATION; CHILD; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; HEPATOMEGALY; HUMANS; IMMUNOPHENOTYPING; ISOCHROMOSOMES; LIVER NEOPLASMS; LYMPHOMA, T-CELL; MONOSOMY; RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA; RECEPTORS, IGG; REMISSION INDUCTION; SPLENIC NEOPLASMS; SPLENOMEGALY; TRANSLOCATION, GENETIC; TRANSPLANTATION, HOMOLOGOUS; TRISOMY; TUMOR STEM CELLS; X CHROMOSOME;

EID: 0036170857     PISSN: 01928562     EISSN: None     Source Type: Journal    
DOI: 10.1097/00043426-200202000-00020     Document Type: Article

References (20)

1. Jaffe ES, Krenacs L, Kumar S, et al. Extranodal peripheral T-cell and NK-cell neoplasms. Am J Clin Pathol 1999; 111(S1): S46-55.
2. Yao M, Tien HF, Lin MT, et al. Clinical and hematological characteristics of hepatosplenic T gamma/delta lymphoma with isochromosome for long arm of chromosome 7. Leuk Lymphoma 1996; 22: 495-500.
3. Jonveaux P, Daniel MT, Martel V, et al. Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphoma. Leukemia 1996; 10: 1453-5.
4. Cooke CB, Krenacs L, Stetler-Stevenson M, et al. Hepatosplenic T-cell lymphoma: a distinct clinicopathologic entity of cytotoxic gamma delta T-cell origin. Blood 1996; 88: 4265-74.
5. Coventry S, Punnett H, Tomczak E, et al. Consistency of isochromosome 7q and trisomy 8 in hepatosplenic T-cell lymphoma: detection by fluorescence in situ hybridization of a splenic touch-preparation from a pediatric patient. Pediatr Dev Pathol 1999; 2: 478-83.
6. Garcia-Sanchez F, Menarguez J, Cristobal E, et al. Hepatosplenic gamma-delta malignant lymphoma: report of the first case in childhood, including molecular minimal residual disease follow-up. Br J Haematol 1995; 90: 943-6.
7. Alonsozana ELC, Stamberg J, Kumar D, et al. Isochromosome 7q: the primary cytogenetic abnormality in hepatosplenic T cell lymphoma. Leukemia 1997; 11: 1367-93.
8. Francois A, Lesesve JF, Stamatoullas A, et al. Hepatosplenic gamma/delta T-cell lymphoma: a report of two cases in immunocompromised patients, associated with isochromosome 7q. Am J Surg Pathol 1997; 21: 781-90.
9. Salhany K, Feldman M, Kahn M, et al. Hepatosplenic T-cell lymphoma: ultrastructural, immunophenotypic, and functional evidence for cytotoxic T lymphocyte differentiation. Hum Pathol 1997; 28: 674-85.
10. Steinherz PG, Redner A, Steinherz L, et al. Development of a new intensive therapy for acute lymphoblastic leukemia in children at increased risk of early relapse. The Memorial Sloan-Kettering-New York-II protocol. Cancer 1993; 72: 3120-30.
11. Mertens F, Johansson B, Mitelman F. Isochromosomes in neoplasia. Genes Chromosomes Cancer 1994; 10: 221-30.
12. Johannson B, Mertens F, Mitelman F. Cytogenetic deletion maps for hematologic neoplasms: Circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer 1993; 8: 205-18.
13. Garipidou V, Yamada T, Prentice HG, et al. Trisomy 8 in acute lymphoblastic leukemia (ALL): A case report and update of the literature. Leukemia 1990; 10: 717-9.
14. Sohn S, Ahn T, Kim D, et al. Hepatosplenic T-cell lymphoma: prolymphocytic transformation 18 months after splenectomy. Int J Hematol 1997; 66: 227-32.
15. Maurici D, Perez-Atayde A, Grier H, et al. Frequency and implications of chromosome 8 and 12 gains in Ewing sarcoma. Cancer Genet Cytogenet 1998; 100: 106-10.
16. Armengol G, Tarkkanen M, Virolainen M, et al. Recurrent gains of 1q, 8 and 12 in the Ewing family of tumors by comparative genomic hybridization. Br J Cancer 1997; 75: 1403-9.
17. Kwong YL, Wong KF, Chan TK. Trisomy 8 in acute promyelocytic leukemia: an interphase study by fluorescence in situ hybridization. Br J Haematol 1995; 90: 697-700.
18. United Kingdom Cancer Cytogenetics Group (UKCCG). Primary, single, autosomal trisomies associated with haematological disorders. Leuk Res 1992;9: 841-51.
19. Raimondi S, Roberson P, Pui CH, et al. Hyperdiploid (47-50) acute lymphoblastic leukemia in children. Blood 1992; 12: 3245-62.
20. Seghezzi L, Maserati E, Minelli A, et al. Constitutional trisomy 8 as first mutation in multistep carcinogeneis: clinical, cytogenetic, and molecular data on three cases. Genes Chromosomes Cancer 1996: 17: 94-101.