Khan W A, Yu L, Eisenbrey A B, Crisan D, al Saadi A, Davis B H, Hankin R C, Mattson J C
Clinical Pathology Department, William Beaumont Hospital, 3601 W 13 Mile Rd, Royal Oak, MI 48073, USA.
Am J Clin Pathol. 2001 Jul;116(1):41-50. doi: 10.1309/TC9U-FAV7-0QBW-6DFC.
We describe 2 male patients in whom hepatosplenic gamma/delta T-cell lymphoma (HSTL) developed 6 and 10 years after renal transplantation. The onset was abrupt with systemic symptoms, cytopenia, and hepatosplenomegaly. The histologic examination of the spleen (case 1), liver, and bone marrow revealed sinusoidal infiltrates of markedly abnormal lymphocytes. The neoplastic cells in these cases were CD2+, CD3+, CD4-, CD5-, CD7+, CD8+, CD16+, CD56+, beta F1-negative, and TIA-1-negative. Both cases displayed clonal rearrangement of the T-cell receptor (TCR) delta gene and the TCR beta gene. The spleen in case 1 was positive for Epstein-Barr virus genome and showed TCR-gamma gene rearrangement by polymerase chain reaction. Isochromosome 7 [i(7)(q10)] was found in each case. Both patients died within 4 months of diagnosis. HSTL has been reported in only 5 renal transplant recipients. HSTL may be relatively more frequent in immunocompromised patients compared with the general population.
我们描述了2例男性患者,他们在肾移植后6年和10年发生了肝脾γ/δ T细胞淋巴瘤(HSTL)。起病急骤,伴有全身症状、血细胞减少和肝脾肿大。对脾脏(病例1)、肝脏和骨髓进行组织学检查,发现有明显异常淋巴细胞的窦状浸润。这些病例中的肿瘤细胞CD2+、CD3+、CD4-、CD5-、CD7+、CD8+、CD16+、CD56+、βF1阴性、TIA-1阴性。两例均显示T细胞受体(TCR)δ基因和TCRβ基因的克隆性重排。病例1的脾脏Epstein-Barr病毒基因组呈阳性,通过聚合酶链反应显示TCR-γ基因重排。两例均发现7号等臂染色体[i(7)(q10)]。两名患者均在诊断后4个月内死亡。仅在5例肾移植受者中报告过HSTL。与普通人群相比,HSTL在免疫功能低下患者中可能相对更常见。