Molecular genetic data favoring a sequential clonal transformation of a large B cell lymphoma into an anaplastic large T cell lymphoma, ALK-negative

被引:0
|
作者
Vanecek, Tomas [1 ]
Walker, Kimberly [2 ]
Watson, Linden L. [2 ]
Rao, Arundhati [2 ]
Rampisela, Debby [2 ]
Donner, Ludvik R. [2 ]
机构
[1] Charles Univ Prague, Sikls Dept Pathol, Sch Med, Plzen, Czech Republic
[2] Texas A&M Hlth Sci Ctr, Coll Med, Scott & White Healthcare, Dept Pathol, Temple, TX 76504 USA
关键词
Large B cell lymphoma; T lymphocytes; IGK rearrangement; ACUTE LYMPHOBLASTIC-LEUKEMIA; EPSTEIN-BARR-VIRUS; NON-HODGKINS-LYMPHOMA; HISTIOCYTIC SARCOMA; FOLLICULAR LYMPHOMA; COMPOSITE LYMPHOMA; IMMUNOGLOBULIN; DISEASE; REARRANGEMENTS; DIAGNOSIS;
D O I
10.1007/s12308-015-0245-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A large B cell lymphoma with monoclonal rearranged, sequentially identical TRG and near identical IGH genes twice relapsed as an anaplastic large T cell lymphoma, ALK-negative. While these IGH and TRG rearrangements were also detected in both relapsed lymphomas, near identical IGK rearrangement was present in the primary and the first relapse, though not in the second relapse, and identical TRB rearrangement was detected only in both relapses, not in the primary. Normal T lymphocytes were the only T cell component found in the primary lymphoma, thus excluding a possibility that the primary lymphoma was a classic composite B and T cell lymphoma. Our data, particularly, the presence of sequentially identical monoclonal TRG and near identical IGH rearrangement in the primary and both relapsed lymphomas, favor a gradual transformation of a B cell lymphoma into a T cell lymphoma. In our opinion, this previously not described phenomenon likely represents a composite lymphoma in statu nascendi.
引用
收藏
页码:243 / 253
页数:11
相关论文
共 50 条
  • [21] ALK-negative anaplastic large cell lymphoma mimicking a soft tissue sarcoma
    Hudacko, Rachel
    Rapkiewicz, Amy
    Berman, Russell Scott
    Simsir, Aylin
    JOURNAL OF CYTOLOGY, 2011, 28 (04) : 230 - U104
  • [22] Skin involvement in ALK-negative systemic anaplastic large-cell lymphoma
    Hoshina, Daichi
    Arita, Ken
    Mizuno, Osamu
    Fujimoto, Katsuya
    Nishio, Mitsufumi
    Kondo, Takeshi
    Abe, Riichiro
    Shimizu, Hiroshi
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2012, 67 (04) : E159 - E160
  • [23] ALK-negative systemic intravascular anaplastic large cell lymphoma presenting in the skin
    Rieger, K. E.
    Polidore, T.
    Warnke, R.
    Kim, J.
    JOURNAL OF CUTANEOUS PATHOLOGY, 2011, 38 (02) : 216 - 220
  • [24] Progress in the identification of subgroups in ALK-negative anaplastic large-cell lymphoma
    Boddicker, Rebecca L.
    Feldman, Andrew L.
    BIOMARKERS IN MEDICINE, 2015, 9 (08) : 719 - 722
  • [25] Leukemic presentation of a highly aggressive ALK-negative anaplastic large cell lymphoma
    Xu, Danmei
    Naresh, Kikkeri N.
    BLOOD, 2021, 138 (13) : 1198 - 1198
  • [26] Recurrent ALK-Negative Anaplastic Large T-Cell Lymphoma Presenting as Necrotizing Vasculitis
    Nambudiri, Vinod E.
    Aboutalebi, Amir
    Granter, Scott R.
    Saavedra, Arturo
    AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2013, 35 (04) : 512 - 516
  • [27] Primary bone ALK-negative anaplastic T cell lymphoma
    Zablocka, T.
    Isajevs, S.
    Nazarovs, J.
    Repnikovs, A.
    VIRCHOWS ARCHIV, 2019, 475 : S343 - S343
  • [28] ALK-negative anaplastic lymphoma after autologous stem cell transplant for relapsed diffuse large B-cell lymphoma
    Lim, Seah H.
    Guileyardo, Joseph M.
    Graham, Robbie
    Strong, Lorna R.
    Esler, William V.
    LEUKEMIA RESEARCH, 2011, 35 (06) : E59 - E60
  • [29] ALK-negative, T-Cell anaplastic large cell lymphoma with hypocellular and neutrophil-rich features
    Martín, CA
    JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2001, 20 (04) : 615 - 616
  • [30] ALK-negative anaplastic large-cell lymphoma demonstrates similar poor prognosis to peripheral T-cell lymphoma, unspecified
    ten Berge, RL
    de Bruin, PC
    Oudejans, JJ
    Ossenkoppele, GJ
    van der Valk, P
    Meijer, CJLM
    HISTOPATHOLOGY, 2003, 43 (05) : 462 - 469