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Case Reports
. 2018 Sep 20:12:872.
doi: 10.3332/ecancer.2018.872. eCollection 2018.

Use of PEG-asparaginase in a case of Hepatosplenic γδ T-cell lymphoma with long-term remission after stem cell transplantation

Affiliations
Case Reports

Use of PEG-asparaginase in a case of Hepatosplenic γδ T-cell lymphoma with long-term remission after stem cell transplantation

Kai Sun et al. Ecancermedicalscience. .

Abstract

Hepatosplenic γδ T-cell lymphoma (HSTCL) is a rare aggressive peripheral T-cell lymphoma. Prognosis is usually poor with a median survival between 8 and 16 months after traditional chemotherapy. Stem cell transplantation (SCT) is promising and with a more intense induction regimen, has yielded positive results. We report the use of pegylated-asparaginase (PEG-asparaginase) along with a conventional anthracycline-containing regimen in a 51-year-old male who was diagnosed with HSTCL, achieved a complete remission, and subsequently underwent peripheral blood SCT and remained in remission at the time of this case report.

Keywords: Hepatosplenic γδ T-cell lymphoma; pegylated-asparaginase; stem cell transplant.

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References

    1. Vose J, Armitage J, Weisenburger D, et al. International T-Cell Lymphoma Project. International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes. J Clin Oncol. 2008;26(25):4124–4130. doi: 10.1200/JCO.2008.16.4558. - DOI - PubMed
    1. Weidmann E. Hepatosplenic T cell lymphoma. A review on 45 cases since the first report describing the disease as a distinct lymphoma entity in 1990. Leukemia. 2000;14(6):991–997. doi: 10.1038/sj.leu.2401784. - DOI - PubMed
    1. Yabe M, Medeiros LJ, Wang SA, et al. Clinicopathologic, immunophenotypic, cytogenetic, and molecular features of gammadelta T-cell large granular lymphocytic leukemia: an analysis of 14 patients suggests biologic differences with alphabeta T-cell large granular lymphocytic leukemia. Am J Clin Pathol. 2015;144(4):607–619. doi: 10.1309/AJCPJSA1E1YWSZEY. - DOI - PubMed
    1. Belhadj K, Reyes F, Farcet JP, et al. Hepatosplenic gammadelta T-cell lymphoma is a rare clinicopathologic entity with poor outcome: report on a series of 21 patients. Blood. 2003;102(13):4261–4269. doi: 10.1182/blood-2003-05-1675. - DOI - PubMed
    1. Farcet JP, Gaulard P, Marolleau JP, et al. Hepatosplenic T-cell lymphoma: sinusal/sinusoidal localization of malignant cells expressing the T-cell receptor gamma delta. Blood. 1990;75(11):2213–2219. - PubMed

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