Primary Cutaneous B-Cell Lymphoma Complicated by Clonal T-Cell Populations: A Diagnostic Dilemma

被引:2
作者
Symes, Emily [1 ]
Dominiak, Nicole [2 ]
机构
[1] Univ Toledo, Coll Med & Life Sci, Med Ctr, Toledo, OH 43614 USA
[2] Univ Toledo, Dept Pathol, Coll Med & Life Sci, Toledo, OH 43614 USA
关键词
composite lymphoma; cutaneous; B-cell lymphoma; T-cell lymphoma; IMMUNOGLOBULIN GENE REARRANGEMENT; LYMPHOPROLIFERATIVE DISORDERS; DUAL GENOTYPE;
D O I
10.1097/DAD.0000000000001906
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Cutaneous lymphomas, both B-cell and T-cell, are not uncommonly seen in the skin, but those lymphomas exhibiting clonality for both B-cell and T-cell populations are scarce. Characterization of dual receptor rearrangement as primary composite lymphoma versus primary lymphoma with reactionary response is complex and often a challenge that goes unrecognized. In this study, we report a unique case of T-cell gene rearrangement positivity complicating the diagnosis of primary cutaneous low-grade B-cell lymphoma along with a review of reported cases containing dual receptor rearrangement to identify trends among final diagnostic decisions. As one might guess, for cutaneous lymphomas presenting with clonality for both T-cell and B-cell receptors, diagnosis can be difficult and confusing because the differential is broad. The literature suggests the majority of these cases may be cutaneous composite lymphomas. However, immunohistochemical, clinical, and histomorphologic features must all be assessed for an accurate diagnosis, which is critical for proper prognosis and therapy.
引用
收藏
页码:454 / 458
页数:5
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