Farcet J P, Kuentz M, Andre C, Darves J M, Reyes F, Dreyfus B, Rochant H
Am J Hematol. 1983 Dec;15(4):403-11. doi: 10.1002/ajh.2830150413.
A new T-cell disorder has recently emerged: the so-called adult T-cell lymphoma leukemia (ATLL) initially described in Japan. Subsequently, ATLL cases were recognized in patients from the Caribbean. We summarize the clinical and hematological features of 19 published cases from Western countries, in addition to a new case we encountered. The leukemic cells display characteristic morphological features and a T3+T4+T8-T6- surface antigenic phenotype. Overall survival is of short duration, but remission could be obtained in our case despite a subsequent relapse in skin and CNS. Geographic clusters of ATLL cases have led to the discovery of the possible role of a new retrovirus, HTLV, in the genesis of this rare malignancy.
一种新的T细胞疾病最近出现了:即最初在日本被描述的所谓成人T细胞淋巴瘤白血病(ATLL)。随后,在来自加勒比地区的患者中也发现了ATLL病例。除了我们遇到的1例新病例外,我们还总结了西方国家19例已发表病例的临床和血液学特征。白血病细胞呈现出特征性的形态学特征以及T3+T4+T8-T6-表面抗原表型。总体生存期较短,但在我们的病例中尽管随后皮肤和中枢神经系统复发仍获得了缓解。ATLL病例的地理聚集导致发现了一种新的逆转录病毒——人类嗜T淋巴细胞病毒(HTLV)在这种罕见恶性肿瘤发生过程中可能发挥的作用。