Bernhards J, Fischer R, Werner M, Hübner K, Schwarze E W, Georgii A
Pathologisches Institut, Medizinischen Hochschule Hannover.
Verh Dtsch Ges Pathol. 1992;76:159-63.
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.
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。