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International Journal of Hematology
/10.1007/s12185-018-02589-4
GUIDE LINE
JSH practical guidelines for hematological malignancies, 2018: 7.
Peripheral T-cell lymphoma (PTCL)
1 2
Motoko Yamaguchi · Ritsuro Suzuki
Received: 28 November 2018 / Accepted: 28 November 2018
© Japanese Society of Hematology 2019
Overview LDH level institutional upper limit of normal, and bone
marrow involvement [5].
The 2017 WHO Classifcation lists approximately 30 disease The Lugano classifcation (2014) also includes response
entities under the category of peripheral T-cell lymphomas criteria for PTCL that incorporates positron-emission
(PTCLs) and natural killer (NK) cell neoplasms [1]. The tomography fndings [4].
entity-specifc prevalence is known to difer between world Note: rare PTCL entities accounting for less than 5% of
regions. The International T-Cell Lymphoma Project, a all T/NK-cell neoplasms in the International T-Cell Lym-
global retrospective study of approximately 1300 patients, phoma Project include enteropathy-associated T-cell lym-
found that the most prevalent PTCL entities in western phoma (EATL), hepatosplenic T-cell lymphoma (HSTL),
countries, from highest to lowest prevalence, were PTCL primary cutaneous ALCL, and subcutaneous panniculitis-
not otherwise specifed (PTCL-NOS), angioimmunoblastic like T-cell lymphoma [2]. EATL accounts for 9.1% of all
T-cell lymphoma (AITL), ALK-positive anaplastic large lymphomas in Europe, where celiac disease is prevalent, and
cell lymphoma (ALCL), and ALK-negative ALCL [2]. This for 5.8% in North America, but is uncommon in Asia at only
chapte
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