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作 者:王可欣[1] 苏琦[1] 周秀田[1] 李一琴[1]
机构地区:[1]衡阳医学院附二医院儿科,衡阳医学院肿瘤研究所
出 处:《癌症》1995年第6期446-449,共4页Chinese Journal of Cancer
摘 要:本文对44例儿童恶性淋巴瘤进行免疫病理分类和临床病理分析。结果表明,临床主要表现浅表淋巴结肿大、消溲、苍白、发热及腹腔肿块。非何杰金氏淋巴瘤(NHL)33例,全部为弥漫型,其中B淋巴瘤18例,裂,无裂细胞性和无裂细胞性各7例;T淋巴瘤14例,大部分为淋巴母细胞性(12例);组织细胞性1例,何杰金氏淋巴瘤(HL)11例,混合细胞型6例,结节硬化型5例。NHL与HL的男女之比分别是2.67:1与4.5:1,高发年龄各为6~13岁与9~13岁。原发部位:结内32例,大部在颈部(20)例);结外11例,多为腹腔(7例)。9例NHI。广泛侵犯骨髓、肝、脾,导致淋巴瘤性白血病。cases of childern with malignant lyphoma(ML) were studied by immunopathologic classification according to Chengdu working Formulation and Clinicopathologic analysis.Predominate clianic manifectations were superficical lymphadenopathy,weight,loss,fever,anemia and abdominal mass;NHL 33 cases(75%),all were diffuse type,of which 18 cases(54.6%)were B cell type,including cases of cleaved-noncleaved and 7 cases of noncleaved, T Cell type 14 cases (42.4),mostly lymphoblastic 12 cases,and histiocyte lcase( 3%);HL ll cases,of which mixed 6 cases and nodulal selerosis 5 cases;male to female radio,the age distribution and the primary sides of NHL and HL were also analysed.
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