Cavdar A O, Arcasoy A, Babacan E, Gözdaşoğlu S, Topuz U, Fraumeni J F
Cancer. 1978 Apr;41(4):1606-9. doi: 10.1002/1097-0142(197804)41:4<1606::aid-cncr2820410451>3.0.co;2-y.
In a series of 166 leukemic children from Turkey, 56 had acute myelomonocytic leukemia (AMML). Seventeen boys and 3 girls presented with chloroma-like deposits (granulocytic or myeloid sarcomas) in the eye and orbit, all showing AMML on initial study of blood and marrow. The ocular lesions responded rapidly to antileukemic therapy. Laboratory studies of AMML cases revealed no cytogenetic or immune defects, and Epstein-Barr virus titers were normal. A group-specific (GS-3) antigen (type-C virus?) was identified in one patient by radioimmunoassay of orbital tumor extracts. It is not clear what factors contribute toward the myelomoncytic differentiation of leukemia and its localization in the eye and orbit, but opportunities for further study are enhanced by reports of a predisposition to ocular chloroma among leukemic children in Africa, Egypt, and Japan.
在来自土耳其的166名白血病儿童中,56名患有急性粒单核细胞白血病(AMML)。17名男孩和3名女孩眼部和眼眶出现绿色瘤样沉积物(粒细胞性或髓细胞肉瘤),在对血液和骨髓进行初步检查时均显示为AMML。眼部病变对抗白血病治疗反应迅速。对AMML病例的实验室研究未发现细胞遗传学或免疫缺陷,爱泼斯坦-巴尔病毒滴度正常。通过对眼眶肿瘤提取物进行放射免疫测定,在一名患者中鉴定出一种群特异性(GS-3)抗原(C型病毒?)。尚不清楚哪些因素导致白血病的粒单核细胞分化及其在眼部和眼眶的定位,但非洲、埃及和日本白血病儿童易患眼部绿色瘤的报道增加了进一步研究的机会。