Geographic Variability of Nodular Lymphocyte-Predominant Hodgkin Lymphoma A Clinicopathologic Reappraisal in the Modern Era

被引:3
作者
Xia, Daniel [1 ]
Sayed, Shahin [2 ]
Moloo, Zahir [2 ]
Gakinya, Samuel M. [2 ]
Mutuiri, Anderson [2 ]
Wawire, Jonathan [2 ]
Okiro, Patricia [2 ]
Courville, Elizabeth L. [3 ]
Hasserjian, Robert P. [4 ,5 ]
Sohani, Aliyah R. [4 ,5 ]
机构
[1] Univ Hlth Network, Div Hematopathol & Transfus Med, Toronto, ON, Canada
[2] Aga Khan Univ Hosp, Nairobi, Kenya
[3] Univ Virginia, Dept Pathol, Charlottesville, VA 22903 USA
[4] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[5] Harvard Med Sch, Boston, MA 02114 USA
关键词
Nodular lymphocyte-predominant Hodgkin lymphoma; Classic Hodgkin lymphoma; Epstein-Barr virus; IgD; T cell rich; Low; middle-income country; EPSTEIN-BARR-VIRUS; B-CELL LYMPHOMA; PROGNOSTIC IMPACT; VARIANT PATTERNS; EBV INFECTION; DISEASE; CHILDREN; EXPRESSION; TUMOR; KENYA;
D O I
10.1093/ajcp/aqab113
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Objectives Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) differs from classic Hodgkin lymphoma (CHL) in terms of clinicopathologic features, including Epstein-Barr virus (EBV) association. CHL geographic variability is well known, with higher frequencies of mixed-cellularity subtype and EBV positivity in low/middle-income countries (LMICs), but there are few well-characterized series of NLPHL from LMICs. Methods We detail clinicopathologic findings of 21 NLPHL cases received in consultation from Kenya and summarize reports of NLPHL with EBV testing published since 2000. Results Median age of consultation cases was 36 years, and male/female ratio was 3.2. All cases involved peripheral lymph nodes and showed at least some B-cell-rich nodular immunoarchitecture, with prominent extranodular lymphocyte-predominant (LP) cells and T-cell-rich variant patterns most commonly seen. LP cells expressed pan-B-cell markers, including strong OCT2; lacked CD30 and CD15 expression in most cases; and were in a background of expanded/disrupted follicular dendritic cell meshworks and increased T-follicular helper cells. LP cells were EBV negative in 18 cases. Historical cases showed a low rate of EBV positivity with no significant difference between LMICs and high-income countries. Conclusions Unlike CHL, NLPHL shows few geographic differences in terms of clinicopathologic features and EBV association. These findings have implications for diagnosis, prognostication, and treatment of patients with NLPHL in LMICs.
引用
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页码:231 / 243
页数:13
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