Tamaru Jun-Ichi, Tokuhira Michihide, Nittsu Nozomi, Nakamura Shigeo, Ichinohasama Ryo, Suzuki Ritsuro, Mori Hiraki, Takagi Toshiyuki, Suzuki Takahiro, Itami Jun, Itoyama Shinji, Mikata Atsuo
Department of Pathology, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan.
Leuk Lymphoma. 2007 Jun;48(6):1127-38. doi: 10.1080/10428190701342000.
In the WHO classification, the majority of Hodgkin-like ALCL cases as defined by the REAL classification are considered to be CHL. However, establishing a histological diagnosis for the gray zone between CHL and ALCL is often confusing. In this study, we re-evaluated such cases by performing immunohistochemistry with antibodies against PAX-5/BSAP, Oct.2, and BOB.1/OBF.1. Expression of PAX-5/BSAP was observed in 88% (76/87) of CHL specimens and none (0/11) of ALK-positive ALCL specimens. Among specimens of Hodgkin-like ALCL and ALK-negative ALCL, expression of PAX-5/BSAP was observed in 77% (20/26) and 18% (3/17), respectively. Most of the PAX-5/BSAP-positive specimens were negative for Oct.2 and/or BOB.1/OBF.1 except for four CHL specimens. Our results may support the WHO classification in which most cases of Hodgkin-like ALCL are classified as CHL. However, the patients with Hodgkin-like ALCL with CHL-immunophenotype (PAX-5/BSAP-positive and negative for Oct.2 and/or BOB.1) did not have a favorable outcome, with a 5-year OS rate of 58%.
在世界卫生组织(WHO)分类中,按照修订的欧美淋巴瘤分类(REAL分类)定义的大多数霍奇金样间变性大细胞淋巴瘤(ALCL)病例被认为是经典型霍奇金淋巴瘤(CHL)。然而,对CHL和ALCL之间的灰色地带进行组织学诊断往往令人困惑。在本研究中,我们通过使用抗PAX-5/BSAP、Oct.2和BOB.1/OBF.1的抗体进行免疫组织化学,对这些病例进行了重新评估。在88%(76/87)的CHL标本中观察到PAX-5/BSAP表达,而在间变性淋巴瘤激酶(ALK)阳性的ALCL标本中均未观察到(0/11)。在霍奇金样ALCL和ALK阴性ALCL标本中,PAX-5/BSAP表达分别在77%(20/26)和18%(3/17)中观察到。除4例CHL标本外,大多数PAX-5/BSAP阳性标本Oct.2和/或BOB.1/OBF.1呈阴性。我们的结果可能支持WHO分类,其中大多数霍奇金样ALCL病例被分类为CHL。然而,具有CHL免疫表型(PAX-5/BSAP阳性且Oct.2和/或BOB.1阴性)的霍奇金样ALCL患者预后不佳,5年总生存率为58%。