Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Am J Surg Pathol. 2012 May;36(5):716-25. doi: 10.1097/PAS.0b013e3182487158.
An association between classical Hodgkin lymphoma (cHL) and mycosis fungoides (MF) or lymphomatoid papulosis has been reported in the literature. However, there can be considerable morphologic and immunophenotypic overlap between cHL and nodal involvement by CD30-positive T-cell lymphoproliferative disorders (CD30-T-LPD). To examine this potential association, biopsies from patients with a history of MF or primary cutaneous CD30-T-LPD and lymph node biopsies reported as either CD30-positive T-cell lymphoma (TCL) with Hodgkin-like cells or cHL were retrieved from the authors' institution. Of 11 cases identified, 10 were considered CD30-positive TCL with Hodgkin-like cells, whereas 1 was confirmed as cHL upon review. Five cases originally diagnosed as cHL were revised as CD30-positive TCL. Cases of CD30-positive TCL with Hodgkin-like cells showed a male predominance (M:F, 4:1) with a median age of 53 years (range, 44 to 72 y). Nearly all patients (9/10) initially presented with skin lesions. In 7/10 patients the draining lymph node was involved, whereas in 3 cases this could not be confirmed. Tumor cells morphologically resembled Hodgkin/Reed-Sternberg cells; they were uniformly strongly positive for CD30, and CD15 was expressed in 9/10 (90%) cases. A T-cell derivation was confirmed by T-cell antigen expression (7/10) and clonal rearrangement of T-cell receptor genes (9/10). In 3 cases a common T-cell clone was identified in skin and lymph node. B-cell markers (CD20/PAX5) were consistently negative. In 1 case the diagnosis of cHL followed by lymphomatoid papulosis was confirmed, with Hodgkin/Reed-Sternberg cells expressing PAX5, CD30, and CD15. In situ hybridization studies for Epstein Barr virus were negative. We show that cHL is less often associated with MF and primary cutaneous CD30-T-LPD than previously thought and that the coexpression of CD30 and CD15 in these TCLs may lead to a mistaken diagnosis of cHL.
经典霍奇金淋巴瘤(cHL)与蕈样真菌病(MF)或淋巴母细胞性丘疹病(LPP)之间的关联在文献中有报道。然而,cHL 与 CD30 阳性 T 细胞淋巴增生性疾病(CD30-T-LPD)的淋巴结受累之间可能存在相当大的形态学和免疫表型重叠。为了研究这种潜在的关联,从作者所在机构的 MF 病史或原发性皮肤 CD30-T-LPD 患者的活检以及报告为 CD30 阳性 T 细胞淋巴瘤(TCL)伴霍奇金样细胞或 cHL 的淋巴结活检中检索到了活检。在确定的 11 例病例中,10 例被认为是 CD30 阳性 TCL 伴霍奇金样细胞,而 1 例经复查后确认为 cHL。5 例最初诊断为 cHL 的病例被修订为 CD30 阳性 TCL。CD30 阳性 TCL 伴霍奇金样细胞的病例表现为男性为主(M:F,4:1),中位年龄为 53 岁(范围,44 至 72 岁)。几乎所有患者(9/10)最初均表现为皮肤病变。在 10 例中有 7 例累及引流淋巴结,而在 3 例中无法确认。肿瘤细胞形态上类似于霍奇金/里斯滕伯格细胞;它们均强烈表达 CD30,9/10(90%)病例表达 CD15。通过 T 细胞抗原表达(7/10)和 T 细胞受体基因的克隆重排(9/10)证实了 T 细胞的来源。在 3 例中,在皮肤和淋巴结中发现了共同的 T 细胞克隆。B 细胞标志物(CD20/PAX5)始终为阴性。在 1 例病例中,经证实存在 cHL 继发淋巴母细胞性丘疹病,霍奇金/里斯滕伯格细胞表达 PAX5、CD30 和 CD15。原位杂交研究 Epstein Barr 病毒为阴性。我们表明,cHL 与 MF 和原发性皮肤 CD30-T-LPD 的关联比以前认为的要少,这些 TCL 中 CD30 和 CD15 的共表达可能导致对 cHL 的误诊。