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. 2021 Mar 18;61(1):35–41. doi: 10.3960/jslrt.20062

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© 2021 by The Japanese Society for Lymphoreticular Tissue Research

This is an open-access article distributed under the terms of the Creative Commons Attribution ShareAlike (CC BY-NC-SA) 4.0 License.

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Fig. 1 — The OS of BCL patients including MCL, FL grade 3, MZL, DLBCL, unclassified BCL, and PT/NKCL. The PT/NKCL group included 53 patients with PTCL-NOS, 46 with angioimmunoblastic T-cell lymphoma, 18 with anaplastic large cell lymphoma, 17 with extranodal NK/T-cell lymphoma nasal type, one with subcutaneous panniculitis-like T-cell lymphoma, and one with enteropathy-type T-cell lymphoma as described in a previous report [11]. The OS of BCL patients including MCL, FL grade 3, MZL, DLBCL, unclassified BCL, and PT/NKCL. The PT/NKCL group included 53 patients with PTCL-NOS, 46 with angioimmunoblastic T-cell lymphoma, 18 with anaplastic large cell lymphoma, 17 with extranodal NK/T-cell lymphoma nasal type, one with subcutaneous panniculitis-like T-cell lymphoma, and one with enteropathy-type T-cell lymphoma as described in a previous report [11].