Kremer M, Sandherr M, Geist B, Cabras A D, Höfler H, Fend F
Institute of Pathology, Technical University Munich, Germany.
Mod Pathol. 2001 Feb;14(2):91-7. doi: 10.1038/modpathol.3880262.
The association of mycosis fungoides (MF) and Hodgkin's lymphoma is a relatively frequent occurrence, but the potential clonal relationship of the two neoplasms is still controversial. We report a case of a patient with a history of MF in Clinical Stage 1A who developed retroperitoneal lymphadenopathy 9 years after the initial diagnosis of MF. A bone marrow biopsy obtained at this time showed nodular involvement by a mixed cellular infiltrate with large, atypical cells consistent with Hodgkin and Reed-Sternberg (RS) cells. These atypical cells were positive for CD30 and CD15 and did not express B- or T-cell markers. In addition, they lacked evidence of infection by Epstein-Barr virus, both by immunohistochemical staining for latent membrane protein 1 and by in situ hybridization for EBER1/2. The background population consisted mainly of small T cells without morphological or phenotypical signs of malignancy. Review of the skin biopsy obtained 9 years before showed the typical features of MF. Polymerase chain reaction analysis of the T-cell receptor T-gene confirmed the presence of a clonal T-cell rearrangement in the skin specimen. The bone marrow biopsy, however, showed a polyclonal pattern both for the T-cell receptor gamma-gene, as well as for immunoglobulin heavy chain genes. Isolation of RS cells stained for CD30 was performed by laser capture microdissection. Polymerase chain reaction analysis of several groups of RS cells showed a reproducible biallelic rearrangement of IgH genes, which was confirmed by cloning and sequencing of polymerase chain reaction products. To our knowledge, this is the first case in which a distinct clonal origin of MF and Hodgkin's lymphoma arising in the same patient is clearly demonstrated, based on molecular analysis of microdissected RS cells.
蕈样肉芽肿(MF)与霍奇金淋巴瘤的关联较为常见,但这两种肿瘤潜在的克隆关系仍存在争议。我们报告一例临床1A期MF患者,在MF初诊9年后出现腹膜后淋巴结病。此时进行的骨髓活检显示,混合细胞浸润呈结节状累及,其中有与霍奇金和里德-斯腾伯格(RS)细胞一致的大的非典型细胞。这些非典型细胞CD30和CD15呈阳性,不表达B或T细胞标志物。此外,通过潜伏膜蛋白1的免疫组化染色和EBER1/2的原位杂交,均未发现它们有EB病毒感染的证据。背景细胞群主要由小T细胞组成,无恶性形态学或表型特征。回顾9年前获取的皮肤活检标本显示有MF的典型特征。T细胞受体T基因的聚合酶链反应分析证实皮肤标本中存在克隆性T细胞重排。然而,骨髓活检显示T细胞受体γ基因以及免疫球蛋白重链基因均呈多克隆模式。通过激光捕获显微切割分离出CD30染色的RS细胞。对几组RS细胞进行聚合酶链反应分析显示IgH基因存在可重复的双等位基因重排,这通过聚合酶链反应产物的克隆和测序得以证实。据我们所知,这是首例基于显微切割RS细胞的分子分析,明确显示同一患者中MF和霍奇金淋巴瘤有不同克隆起源的病例。