Human Pathology
Volume 41, Issue 9 , Pages 1231-1237, September 2010

Enteropathy-associated T-cell lymphoma—a clinicopathologic and array comparative genomic hybridization study☆☆

  • Young Hyeh Ko, MD, PhD

      Affiliations

    • Department of Pathology, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
    • Corresponding Author InformationCorresponding authors. Young Hyeh Ko is to be contacted at Department of Pathology, Samsung Medical Center, Sungkyunkwan University, Kangnamgu, Seoul, 135-710, Korea. Masao Seto, Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya 464-8681, Japan.
  • ,
  • Sivasundaram Karnan

      Affiliations

    • Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya 464-8681, Japan
  • ,
  • Kyeong Mee Kim, MD, PhD

      Affiliations

    • Department of Pathology, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Cheol Keun Park, MD, PhD

      Affiliations

    • Department of Pathology, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Eun Suk Kang, MD, PhD

      Affiliations

    • Laboratory Medicine, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Young Ho Kim, MD, PhD

      Affiliations

    • Division of Gastroenterology, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Won Ki Kang, MD, PhD

      Affiliations

    • Division of Gastroenterology, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Seok Jin Kim, MD, PhD

      Affiliations

    • Hemato-oncology of Internal Medicine, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Won Seog Kim, MD, PhD

      Affiliations

    • Hemato-oncology of Internal Medicine, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Woo Yong Lee, MD, PhD

      Affiliations

    • General surgery, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Ho Kyung Chun

      Affiliations

    • General surgery, Samsung Medical Center, Sungkyunkwan University, Seoul 135-710, Korea
  • ,
  • Masao Seto, MD, PhD

      Affiliations

    • Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya 464-8681, Japan
    • Corresponding Author InformationCorresponding authors. Young Hyeh Ko is to be contacted at Department of Pathology, Samsung Medical Center, Sungkyunkwan University, Kangnamgu, Seoul, 135-710, Korea. Masao Seto, Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya 464-8681, Japan.

Received 13 July 2009; received in revised form 9 November 2009; accepted 20 November 2009. published online 19 April 2010.

Summary 

According to the new World Health Organization classification system, there are 2 types of enteropathy-associated T-cell lymphoma. Type 1 is associated with celiac disease and accounts for the majority of cases in Western countries, whereas type 2 is not associated with celiac disease. To characterize enteropathy-associated T-cell lymphoma types in Korea, we carried out clinicopathologic and immunophenotypic analyses of 8 Koreans with enteropathy-associated T-cell lymphoma and investigated genomic profile using array comparative genomic hybridization. The tumors involved the small intestine in 5 patients and the colorectum in 3 patients. Two patients carried an HLA DQB1⁎0302 allele that corresponds to HLA DQ8. None of the patients had gluten-sensitive malabsorption syndrome. Intraepithelial lymphocytosis was observed in all patients. The sizes of the tumor cells were small or small-to-medium in 7 cases and medium-to-large in 1 case. The immunophenotypes of the tumor cells were CD4−CD8+CD56+ in 4 cases, CD4−CD8+CD56− in 1 case, CD4−CD8−CD56+ in 2 cases, and CD4−CD8−CD56− in 1 case. Array comparative genomic hybridization analysis showed that chromosome 9q33-q34.1 gain was present in 4 (80%) of the 5 cases examined. Other recurrent genomic alterations were gain of 6p21.1-21.31 (3/5, 60%), gain of 19q (2/5), and the loss of 3p12.1-p12.2 (2/5) and 3q26.31 (2/5). These results suggest that the most prevalent type of enteropathy-associated T-cell lymphoma in this geographic region is type 2, and the genetic changes associated with it are similar to those in Western countries.

Keywords: Lymphoma, Intestine, Enteropathy, Array comparative genomic hybridization

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 The authors have no conflict of interest to disclosure.

☆☆ This work was supported by a grant from Samsung Biomedical Research Institute, Seoul, Korea (SBRI C-A8-202).

PII: S0046-8177(10)00050-X

doi:10.1016/j.humpath.2009.11.020

Human Pathology
Volume 41, Issue 9 , Pages 1231-1237, September 2010