Post-transplant Lymphoproliferative Disorder Presented in a Form of Primary Effusion Lymphoma with t (8;14)

被引:0
|
作者
Sultana, Sadia [1 ]
Al Salihi, Suhair [1 ]
Tandon, Nidhi [1 ]
Jaso, Jesse [1 ]
Nguyen, Nghia D. [1 ]
Zhang, Songlin [1 ]
Liu, Jing [1 ]
机构
[1] UTHlth McGovern Med Sch, Dept Pathol & Lab Med, 6431 Fannin St,MSB 2-202, Houston, TX 77030 USA
来源
关键词
Post-transplant lymphoproliferative disorder (PTLD); Primary effusion lymphoma (PEL); positive EBV; negative HHV8; t(8; 14); HEPATITIS-C VIRUS; DISTINCT ENTITY; LIVER-CIRRHOSIS; HERPES-VIRUS; PATIENT; RECIPIENTS; HIV;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Post-transplant lymphoproliferative disorders (PTLD) are emergent complications of organ transplantation occurring in 2% to 10% of transplanted patients. Epstein-Barr virus (EBV) infections are considered the most important factors for the development of these heterogeneous disorders. Primary effusion lymphoma (PEL) is a lymphoproliferative disorder predominantly described in patients with advanced AIDS and it is almost universally associated with human herpesvirus 8 (HHV8). In rare case, PEL also occurs in HHV8-negative patient, in the setting of hepatitis B and C virus infection. However, all these cases showed pan B-cell markers to be positive. Here, we report a case of PTLD presented as HHV8 negative and HIV-negative primary effusion lymphoma lacking near all lymphoid markers except PAX5 on immunohistochemistry, which created a diagnostic challenge. The diagnosis requires multiple approaches including molecular and genetic tests.
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收藏
页码:344 / 348
页数:5
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