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Molecular genetic and cytogenetic analysis of a primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma.
Kato, Keisuke; Oh, Yukiko; Takita, Junko; Gunji, Yuji; Kobayashi, Chie; Yoshimi, Ai; Nakao, Tomohei; Noma, Mio; Koike, Kazutoshi; Morimoto, Akira; Iijima, Shigeko; Hojo, Hiroshi; Tsuchida, Masahiro.
Affiliation
  • Kato K; Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Futaba-dai 3-3-1, Mito, Ibaraki, 311-4145, Japan. k-kato@ibaraki-kodomo.com.
  • Oh Y; Department of Pediatrics, Jichi Medical University School of Medicine, Shimotsuke, Japan.
  • Takita J; Department of Cell Therapy and Transplantation, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Gunji Y; Department of Pediatrics, Jichi Medical University School of Medicine, Shimotsuke, Japan.
  • Kobayashi C; Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Futaba-dai 3-3-1, Mito, Ibaraki, 311-4145, Japan.
  • Yoshimi A; Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Futaba-dai 3-3-1, Mito, Ibaraki, 311-4145, Japan.
  • Nakao T; Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Futaba-dai 3-3-1, Mito, Ibaraki, 311-4145, Japan.
  • Noma M; Division of Cardiovascular Surgery, Ibaraki Children's Hospital, Mito, Japan.
  • Koike K; Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Futaba-dai 3-3-1, Mito, Ibaraki, 311-4145, Japan.
  • Morimoto A; Department of Pediatrics, Jichi Medical University School of Medicine, Shimotsuke, Japan.
  • Iijima S; Division of Dermatology, Mito Saiseikai Hospital, Mito, Japan.
  • Hojo H; Division of Pathology, Fukushima Prefectural University Hospital, Fukushima, Japan.
  • Tsuchida M; Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Futaba-dai 3-3-1, Mito, Ibaraki, 311-4145, Japan.
Int J Hematol ; 103(2): 196-201, 2016 Feb.
Article in En | MEDLINE | ID: mdl-26676804
ABSTRACT
We performed cytogenetic and molecular cytogenetic analyses of a primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma, a rare type of primary cutaneous T-cell lymphoma. G-banded analysis at initial diagnosis and recurrence revealed complex karyotype and clonal evolution reflecting genomic instability that parallels the aggressive clinical course observed. Spectral karyotyping revealed numerous structural abnormalities. SNP array-based analysis of an initial diagnostic sample revealed numerous gains and losses of chromosomal material, including loss of short arm of the chromosome 17, to which TP53 is mapped. The molecular cytogenetics and array data of this case suggest genomic instability, particularly chromosomal instability and haploinsufficiency for TP53, the latter possibly giving rise to alteration of p14ARF-Mdm2-p53 tumor suppressor protein pathway, likely to be associated with unfavorable clinical course.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, T-Cell, Cutaneous / CD8 Antigens / Cytogenetic Analysis Limits: Child / Female / Humans Language: En Journal: Int J Hematol Journal subject: HEMATOLOGIA Year: 2016 Type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, T-Cell, Cutaneous / CD8 Antigens / Cytogenetic Analysis Limits: Child / Female / Humans Language: En Journal: Int J Hematol Journal subject: HEMATOLOGIA Year: 2016 Type: Article Affiliation country: Japan