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儿童非霍奇金淋巴瘤

Non-Hodgkin's lymphoma in children.

作者信息

Pinkel D, Johnson W, Aur R J

出版信息

Br J Cancer Suppl. 1975 Mar;2:298-323.

Abstract

The clinical and pathological features of 64 children with non-Hodgkin's malignant lymphoma seen between April 1962 and June 1973 are described. Forty-one children had diffuse, undifferentiated, non-Burkitt lymphoma (lymphoblastic lymphoma). They tended to be boys under 10 years of age and their median survival was 1 year. Almost one-third are surviving for 1-11 years, most in initial complete remission. Nineteen children had diffuse, poorly differentiated, histiocytic lymphoma. They tended to be boys more than 10 years of age, their median survival was only 6 months, and only the 3 patients with Stage I peripheral node tumour survived. Two children had nodular, lymphocytic, poorly differentiated lymphoma and 2 had lymphoma resembling the Burkitt type. From our clinical and pathological observations, we conclude that non-Hodgkin's malignant lymphomata in children cannot be separated from the acute lymphocytic, histiocytic and unclassified leukaemias by cytological or histological methods. What is called diffuse, undifferentiated, non-Burkitt type, or lymphoblastic lymphoma is actually acute lymphocytic leukaemia without apparent invasion of marrow and peripheral blood by neoplastic lymphocytes at time of diagnosis. What is termed diffuse, histiocytic lymphoma is acute histiocytic leukaemia without apparent infiltration of marrow and peripheral blood at initial presentation. One could say just as well that acute lymphocytic leukaemia is Stage IV lymphoblastic lymphoma and that acute histiocytic leukaemia is Stage IV histiocytic lymphoma. Further classification of lymphocytic and histiocytic cancers by newer functional, chemical and morphological methods should include both what is called lymphocytic or histiocytic leukaemia and what is called non-Hodgkin's lymphoma as one group of diseases, susceptible to subclassification by the new methods. We recommend that Stage I lymphocytic and histiocytic cancers be treated with local irradiation. Patients with Stages II-IV tumours should receive anti-leukaemic forms of therapy including prolonged multiple agent chemotherapy and preventive central nervous system irradiation. Staging laparotomy should be considered in patients with Stage I tumour in low cervical, axillary and inguinal nodes.

摘要

本文描述了1962年4月至1973年6月间收治的64例儿童非霍奇金恶性淋巴瘤的临床和病理特征。41例儿童患有弥漫性、未分化、非伯基特淋巴瘤(淋巴母细胞淋巴瘤)。这些患儿多为10岁以下男孩,中位生存期为1年。近三分之一的患儿存活了1至11年,多数处于初始完全缓解状态。19例儿童患有弥漫性、低分化、组织细胞淋巴瘤。这些患儿多为10岁以上男孩,中位生存期仅6个月,仅3例I期外周淋巴结肿瘤患者存活。2例儿童患有结节性、淋巴细胞性、低分化淋巴瘤,2例患有类似伯基特型的淋巴瘤。根据我们的临床和病理观察,我们得出结论,儿童非霍奇金恶性淋巴瘤无法通过细胞学或组织学方法与急性淋巴细胞性、组织细胞性和未分类白血病相区分。所谓的弥漫性、未分化、非伯基特型或淋巴母细胞淋巴瘤实际上是急性淋巴细胞白血病,在诊断时肿瘤性淋巴细胞未明显侵犯骨髓和外周血。所谓的弥漫性组织细胞淋巴瘤是急性组织细胞白血病,在初次就诊时骨髓和外周血无明显浸润。也可以说急性淋巴细胞白血病是IV期淋巴母细胞淋巴瘤,急性组织细胞白血病是IV期组织细胞淋巴瘤。通过更新的功能、化学和形态学方法对淋巴细胞性和组织细胞性癌症进行进一步分类时,应将所谓的淋巴细胞性或组织细胞性白血病以及所谓的非霍奇金淋巴瘤归为一组疾病,这些疾病易于通过新方法进行亚分类。我们建议I期淋巴细胞性和组织细胞性癌症采用局部放疗。II-IV期肿瘤患者应接受抗白血病治疗,包括延长多药化疗和预防性中枢神经系统放疗。对于低颈、腋窝和腹股沟淋巴结I期肿瘤患者,应考虑进行分期剖腹探查术。

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