Herrmann R, Han T, Barcos M P, Lok M S, Henderson E S
Cancer. 1980 Sep 15;46(6):1383-8. doi: 10.1002/1097-0142(19800915)46:6<1383::aid-cncr2820460616>3.0.co;2-y.
We report a case of a T-zone malignant lymphoma of a cervical lymph node developing in a 25-year-old man. Only 14% of the marrow was originally involved, but within two months massive, leukemic dissemination ensued. The blast cells were unable to bind sheep erythrocytes (E) but expressed human thymus leukemia antigen (HTLA) and common ALL-stem-cell (cALL) antigen and had high terminal deoxynucleotidyl transferase (TdT) and acid phosphatase activity. These findings suggest a malignant lymphoproliferative disorder of pre-T-cell type. Complete remission was achieved with intensive chemotherapy. Two months later, acute myelomonocytic leukemia was diagnosed; at this time, over 90% of the blast cells were peroxidase, sudan black, and chloracetate-esterase positive. Consistent with loss of high TdT activity and HTLA and cALL antigens, 86% of the blasts now expressed Ia-like antigens. Cytogenetic studies demonstrated hyperdiploidy. Reports of granulocytic leukemia in lymphoma are reviewed in the context of the above findings and the hypothesis that a leukemogenic factor affects a multipotential stem cell.
我们报告了一例发生在一名25岁男性颈部淋巴结的T区恶性淋巴瘤病例。最初仅14%的骨髓受累,但在两个月内出现了大量白血病性播散。原始细胞不能结合绵羊红细胞(E),但表达人胸腺白血病抗原(HTLA)和普通急性淋巴细胞白血病干细胞(cALL)抗原,并且具有高末端脱氧核苷酸转移酶(TdT)和酸性磷酸酶活性。这些发现提示为前T细胞型恶性淋巴细胞增殖性疾病。通过强化化疗实现了完全缓解。两个月后,诊断为急性粒单核细胞白血病;此时,超过90%的原始细胞过氧化物酶、苏丹黑和氯乙酸酯酶呈阳性。与高TdT活性以及HTLA和cALL抗原的缺失一致,现在86%的原始细胞表达Ia样抗原。细胞遗传学研究显示为超二倍体。结合上述发现以及白血病致病因子影响多能干细胞的假说,对淋巴瘤中粒细胞白血病的报告进行了综述。