Cerroni L, Beham-Schmid C, Kerl H
Department of Dermatology, University of Graz, Austria.
J Cutan Pathol. 1995 Jun;22(3):229-35. doi: 10.1111/j.1600-0560.1995.tb00743.x.
Studies of skin involvement in Hodgkin's disease are infrequent in the literature. In particular, immunophenotypic analyses of specific cutaneous infiltrates have been performed in only a few cases. We analyzed the clinical, histological and immunohistochemical features of specific cutaneous manifestations of Hodgkin's disease comparing histologic and immunophenotypic aspects of skin lesions with those of the nodal counterpart. Seven patients with Hodgkin's disease of the lymph nodes and specific cutaneous lesions, where both nodal and skin biopsies were available for histologic and immunohistochemical analyses, were included in this study. Immunohistochemical stains were performed with a 3-step immunoperoxidase technique on routinely-fixed, paraffin-embedded tissue sections. All 7 patients had nodular sclerosis Hodgkin's disease of the lymph nodes. In the skin, clinical presentations included reddish-brown papules, plaques, nodules and ulcerated tumors. Histologic examination of cutaneous lesions showed features consistent with nodular sclerosis Hodgkin's disease in 6 cases and unclassifiable Hodgkin's disease in one. Reed-Sternberg cells and lacunar cells were present in 4 cases (57.1%). Immunohistochemical analysis of Hodgkin's and Reed-Sternberg cells revealed a constant positivity for CD30 (BerH2) and negativity for CD45 (LCA) in both the lymph nodes and the skin. Staining with CD15 (M1) revealed positivity in 7/7 nodal samples and 5/7 skin biopsies. Cytoplasmic expression of immunoglobulin light chains (both lambda and kappa) was observed in one cutaneous case. The accompanying infiltrate was mostly composed of T-lymphocytes admixed with variable numbers of monocytes/macrophages and eosinophils. Our results indicate that the histology of cutaneous specific manifestations of Hodgkin's disease correlates with that of the nodal counterpart in most cases.(ABSTRACT TRUNCATED AT 250 WORDS)
关于霍奇金淋巴瘤皮肤受累情况的研究在文献中并不常见。特别是,仅在少数病例中对特定皮肤浸润进行了免疫表型分析。我们分析了霍奇金淋巴瘤特定皮肤表现的临床、组织学和免疫组化特征,将皮肤病变的组织学和免疫表型方面与相应淋巴结病变进行比较。本研究纳入了7例有淋巴结霍奇金淋巴瘤及特定皮肤病变的患者,其淋巴结和皮肤活检标本均可供组织学和免疫组化分析。采用三步免疫过氧化物酶技术对常规固定、石蜡包埋的组织切片进行免疫组化染色。所有7例患者均为淋巴结结节硬化型霍奇金淋巴瘤。皮肤临床表现包括红棕色丘疹、斑块、结节和溃疡肿瘤。6例皮肤病变的组织学检查显示特征与结节硬化型霍奇金淋巴瘤一致,1例为无法分类的霍奇金淋巴瘤。4例(57.1%)存在里德-斯腾伯格细胞和陷窝细胞。对霍奇金细胞和里德-斯腾伯格细胞的免疫组化分析显示,淋巴结和皮肤中CD30(BerH2)均持续阳性而CD45(LCA)均阴性。CD15(M1)染色显示7/7例淋巴结样本和5/7例皮肤活检呈阳性。在1例皮肤病例中观察到免疫球蛋白轻链(λ和κ)的细胞质表达。伴随的浸润主要由T淋巴细胞组成,混有数量不等得单核细胞/巨噬细胞和嗜酸性粒细胞。我们的结果表明,大多数情况下霍奇金淋巴瘤皮肤特定表现的组织学与相应淋巴结病变相关。(摘要截选至250字)