Kuo Tseng-tong, Chen Ming-Jing, Kuo Ming-Chung
Department of Pathology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kwei San, Taoyuan, Taiwan.
Am J Surg Pathol. 2006 Sep;30(9):1197-201. doi: 10.1097/01.pas.0000213263.99973.09.
Intravascular lymphoma (IVL) is a rare variant of non-Hodgkin lymphoma with a predilection for skin and brain. Except a few cases of T-cell lineage, most of the reported cases were large B-cell lymphomas. We encountered a case of cutaneous IVL in a 71-year-old woman presenting with multiple erythematous patches and nodules on her trunk and extremities. The intravascular large cells showed an immunophenotype of CD3epsilon(+);, CD5(-), CD20(-), CD30(-), CD56(+), and TIA-1(+). The lymphoma cells were also positive for Epstein-Barr virus by Epstein-Barr virus-encoded RNA in situ hybridization test and the T-cell receptor gene was germline. This IVL differs from nasal type NK/T-cell lymphoma only by its intravascular nature. Only 3 cases of intravascular NK-cell lymphoma have been reported before. Because this variant is extremely rare, our case is documented and compared with the 3 previously reported cases.
血管内淋巴瘤(IVL)是一种罕见的非霍奇金淋巴瘤变体,好发于皮肤和脑。除少数T细胞谱系病例外,大多数报道的病例为大B细胞淋巴瘤。我们遇到一例71岁女性的皮肤IVL,其躯干和四肢出现多个红斑性斑块和结节。血管内大细胞显示出CD3ε(+)、CD5(-)、CD20(-)、CD30(-)、CD56(+)和TIA-1(+)的免疫表型。通过爱泼斯坦-巴尔病毒编码RNA原位杂交试验,淋巴瘤细胞对爱泼斯坦-巴尔病毒也呈阳性,且T细胞受体基因是种系的。这种IVL仅因其血管内性质与鼻型NK/T细胞淋巴瘤不同。此前仅报道过3例血管内NK细胞淋巴瘤。由于这种变体极其罕见,我们记录了该病例并与之前报道的3例病例进行比较。