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具有不良临床病程的霍奇金淋巴瘤与非霍奇金淋巴瘤的边界:德国霍奇金淋巴瘤研究中33例病例的临床、组织学和免疫组化分析

[Borderline between Hodgkin and non-Hodgkin lymphomas with unfavorable clinical course: a clinical, histological and immunohistochemical analysis of 33 cases within the German Hodgkin Lymphoma Study].

作者信息

Bernhards J, Fischer R, Werner M, Hübner K, Schwarze E W, Georgii A

机构信息

Pathologisches Institut, Medizinischen Hochschule Hannover.

出版信息

Verh Dtsch Ges Pathol. 1992;76:159-63.

PMID:1283250
Abstract

Reevaluation of diagnostic biopsies from 502 patients who entered the German Hodgkin Therapy trial was performed by a panel of four pathologists. Classification revealed 90% of unambiguous Hodgkin-lymphomas (HL), 1.6% of Non-Hodgkin-lymphomas (NHL) and 8.4% of cases difficult to evaluate, reflecting to the well-known problem of the border between these 2 groups of lymphoma. As these cases had the worst prognosis, a second attempt of reclassification, including immunohistochemical studies, was made, resulting in final classifying of 25% of these cases as NHL, 50% as HL, and 25% as further unclassifiable. The most common differential diagnostic problem was separating pleomorphic nodular sclerosing HL from large cell NHL's and HL with rather few Hodgkin- or Reed-Sternberg-cells from Lennerts lymphoma or angioimmunoblastic lymphadenopathy. Immunohistochemistry was helpful for the differential diagnostic decisions in these individual cases. A very high percentage of these problem cases had initially entered the trial as lymphocyte depleted HL, and the large majority of deaths came from the large cell NHL group.

摘要

由四位病理学家组成的小组对参加德国霍奇金淋巴瘤治疗试验的502例患者的诊断性活检样本进行了重新评估。分类结果显示,明确的霍奇金淋巴瘤(HL)占90%,非霍奇金淋巴瘤(NHL)占1.6%,难以评估的病例占8.4%,这反映了这两类淋巴瘤之间界限的著名难题。由于这些病例预后最差,因此进行了第二次重新分类尝试,包括免疫组化研究,最终将其中25%的病例分类为NHL,50%为HL,25%仍无法分类。最常见的鉴别诊断问题是将多形性结节硬化型HL与大细胞NHL区分开来,以及将霍奇金或里德-斯腾伯格细胞较少的HL与 Lennert淋巴瘤或血管免疫母细胞性淋巴结病区分开来。免疫组化有助于这些个别病例的鉴别诊断决策。这些疑难病例中很大一部分最初是以淋巴细胞消减型HL进入试验的,并且大多数死亡病例来自大细胞NHL组。

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