Department of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnan-chou, Joetsu, Niigata 943-0147, Japan.
Int J Hematol. 2013 Feb;97(2):275-9. doi: 10.1007/s12185-013-1262-7. Epub 2013 Jan 29.
We present a case of classical Hodgkin's lymphoma (HL) co-occurring with histological features of Castleman's disease (CD). A 25-year-old man presented with left supraclavicular and axillary lymph node swelling and mediastinal mass. Using an initial biopsy specimen from left axillary lymph node, a tentative diagnosis of multicentric CD of plasma cell type was made. The serum level of interleukin-6 (IL-6) was elevated. The patient was treated with immunosuppressive therapy containing tocilizumab (TCZ). Shrinkage of mediastinal mass and axillary lymph nodes was seen; however, swelling of his left axillary lymph nodes reemerged, even after therapy with TCZ. A second left axillary lymph node biopsy was performed and a diagnosis of nodular sclerosis of classical HL without histologic features of CD was made. The initial biopsy specimen was re-examined, and scattered CD30+ Hodgkin/Reed-Sternberg cells were found in the interfollicular area. Interestingly, Hodgkin/Reed-Sternberg cells and surrounding reactive cells in both lymph nodes were stained with anti-IL-6 antibody. We emphasize that biopsy specimens with HL involvement may also have histologic features reminiscent of those seen in CD. To our knowledge, this is the first report to provide a detailed description of this pathology, including a survey of IL-6 and clinical course upon treatment with TCZ.
我们报告了一例经典霍奇金淋巴瘤(HL)合并 Castleman 病(CD)组织学特征的病例。一名 25 岁男性出现左锁骨上和腋窝淋巴结肿大及纵隔肿块。根据左腋窝淋巴结的初始活检标本,初步诊断为浆细胞型多中心 CD。血清白细胞介素 6(IL-6)水平升高。患者接受了包含托珠单抗(TCZ)的免疫抑制治疗。纵隔肿块和腋窝淋巴结缩小;然而,即使在 TCZ 治疗后,他的左腋窝淋巴结仍出现肿胀。进行了第二次左腋窝淋巴结活检,诊断为无 CD 组织学特征的经典 HL 的结节硬化型。重新检查初始活检标本,在滤泡间区发现散在的 CD30+霍奇金/里德-斯特恩伯格细胞。有趣的是,两个淋巴结中的霍奇金/里德-斯特恩伯格细胞和周围反应性细胞均用抗 IL-6 抗体染色。我们强调,伴有 HL 浸润的活检标本也可能具有类似于 CD 所见的组织学特征。据我们所知,这是第一份详细描述这种病理学的报告,包括对 IL-6 的调查以及 TCZ 治疗后的临床过程。