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成人T细胞白血病-淋巴瘤临床亚型的诊断标准及分类。淋巴瘤研究组报告(1984 - 1987年)

Diagnostic criteria and classification of clinical subtypes of adult T-cell leukaemia-lymphoma. A report from the Lymphoma Study Group (1984-87).

作者信息

Shimoyama M

机构信息

Haematology-Oncology and Medical Oncology Division, National Cancer Center Hospital, Tokyo, Japan.

出版信息

Br J Haematol. 1991 Nov;79(3):428-37. doi: 10.1111/j.1365-2141.1991.tb08051.x.

Abstract

The following diagnostic criteria are proposed to classify four clinical subtypes of HTLV-1 associated adult T-cell leukaemia-lymphoma (ATL): (1) Smouldering type, 5% or more abnormal lymphocytes of T-cell nature in PB, normal lymphocyte level (less than 4 x 10(9)/l), no hypercalcaemia (corrected calcium level less than 2.74 mmol/l), lactate dehydrogenase (LDH) value of up to 1.5 x the normal upper limit, no lymphadenopathy, no involvement of liver, spleen, central nervous system (CNS), bone and gastrointestinal tract, and neither ascites nor pleural effusion. Skin and pulmonary lesion(s) may be present. In case of less than 5% abnormal T-lymphocytes in PB, at least one of histologically-proven skin and pulmonary lesions should be present. (2) Chronic type, absolute lymphocytosis (4 x 10(9)/l or more) with T-lymphocytosis more than 3.5 x 10(9)/l, LDH value up to twice the normal upper limit, no hypercalcaemia, no involvement of CNS, bone and gastrointestinal tract, and neither ascites nor pleural effusion. Lymphadenopathy and involvement of liver, spleen, skin, and lung may be present, and 5% or more abnormal T-lymphocytes are seen in PB in most cases . (3) Lymphoma type, no lymphocytosis, 1% or less abnormal T-lymphocytes, and histologically-proven lymphadenopathy with or without extranodal lesions. (4) Acute type, remaining ATL patients who have usually leukaemic manifestation and tumour lesions, but are not classified as any of the three other types. A total of 818 ATL patients with a mean age of 57 years, newly diagnosed from 1983 to 1987, were analysed by this criteria. There were 448 males and 370 females, and 253 were still alive with a median follow-up time of 13.3 months from diagnosis, while 565 were dead with a median survival time (MST) of 5.4 months. MST was 6.2 months for acute type, 10.2 months for lymphoma type, 24.3 months for chronic type, and not yet reached for smouldering type. Projected 2- and 4-year survival rates were 16.7% and 5.0% for acute type, 21.3% and 5.7% for lymphoma type, 52.4% and 26.9% for chronic type, 77.7% and 62.8% for smouldering type, respectively. Distinct clinical features and laboratory findings of each clinical subtype are described.

摘要

现提出以下诊断标准,用于对人嗜T淋巴细胞病毒1型(HTLV-1)相关成人T细胞白血病-淋巴瘤(ATL)的四种临床亚型进行分类:(1)冒烟型,外周血(PB)中5%或更多具有T细胞性质的异常淋巴细胞,淋巴细胞水平正常(低于4×10⁹/L),无高钙血症(校正钙水平低于2.74 mmol/L),乳酸脱氢酶(LDH)值最高为正常上限的1.5倍,无淋巴结病,无肝、脾、中枢神经系统(CNS)、骨骼及胃肠道受累,无腹水及胸腔积液。可能存在皮肤和肺部病变。若PB中异常T淋巴细胞少于5%,则组织学证实的皮肤和肺部病变中至少应有一项存在。(2)慢性型,绝对淋巴细胞增多症(4×10⁹/L或更多),T淋巴细胞增多超过3.5×10⁹/L,LDH值最高为正常上限的两倍,无高钙血症,无CNS、骨骼及胃肠道受累,无腹水及胸腔积液。可能存在淋巴结病以及肝、脾、皮肤和肺部受累,大多数情况下PB中可见5%或更多异常T淋巴细胞。(3)淋巴瘤型,无淋巴细胞增多症,异常T淋巴细胞占1%或更少,且组织学证实有淋巴结病,有或无结外病变。(4)急性型,其余通常有白血病表现和肿瘤病变但未归类为其他三种类型的ATL患者。对1983年至1987年新诊断的818例平均年龄57岁的ATL患者按此标准进行分析。其中男性448例,女性370例,253例仍存活,自诊断起中位随访时间为13.3个月,565例死亡,中位生存时间(MST)为5.4个月。急性型的MST为6.2个月,淋巴瘤型为10.2个月,慢性型为24.3个月,冒烟型尚未达到。急性型的预计2年和4年生存率分别为16.7%和5.0%,淋巴瘤型分别为21.3%和5.7%,慢性型分别为52.4%和26.9%,冒烟型分别为77.7%和62.8%。描述了各临床亚型独特的临床特征和实验室检查结果。

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