Silva Claudine Yap, Goldberg Lynne J, Mahalingam Meera, Bhawan Jag, Wolpowitz Deon
Department of Dermatology, Dermatopathology Section, Boston University School of Medicine, Boston, MA 02118, USA.
J Cutan Pathol. 2011 Oct;38(10):797-800. doi: 10.1111/j.1600-0560.2011.01756.x. Epub 2011 Aug 4.
Pseudomelanocytic nests in the setting of lichenoid inflammation can mimic atypical melanocytic proliferations. Both melanocytic and cytokeratin immunohistochemical stains may be utilized to differentiate these entities. Unlike true melanocytic nests, pseudomelanocytic nests contain Melanoma Antigen Recognized by T-cells 1 (MART-1)/ Melan-A-positive cells and cells positive for pan-cytokeratins, CD3 and/or CD68. Recently, rare (1-2 cells/nest) microphthalmia- associated transcription factor (MiTF)-positive cells were also reported in pseudomelanocytic nests. We present a 48-year-old man with a 2 × 3 cm violaceous to hyperpigmented, non-blanching, polygonal patch on the neck. Histopathology showed focal epidermal atrophy, irregularly distributed junctional nests and a lichenoid infiltrate with colloid bodies. Immunoperoxidase studies revealed occasional pan-cytokeratin and MART-1/Melan-A-positive staining in nests as well as focal S-100 protein-positive cells. Importantly, the majority of nests showed numerous cells positive for MiTF and SOX10 (>2 cells/nest and some the majority of cells). This combined staining pattern confounds the above-described immunohistochemical distinction between pseudo and true melanocytic nests. Clinically felt to represent unilateral lichen planus pigmentosus/erythema dyschromicum perstans and not malignant melanoma in situ, this lesion highlights the importance of clinicopathologic correlation and suggests either a new melanocytic entity or a novel pattern of benign melanocytic reorganization in a subset of lichenoid dermatitides.
苔藓样炎症背景下的假黑素细胞巢可模拟非典型黑素细胞增殖。黑素细胞和细胞角蛋白免疫组化染色均可用于区分这些病变。与真正的黑素细胞巢不同,假黑素细胞巢含有T细胞识别的黑色素瘤抗原1(MART-1)/黑素-A阳性细胞以及全细胞角蛋白、CD3和/或CD68阳性的细胞。最近,在假黑素细胞巢中也报道了罕见的(每个巢1 - 2个细胞)小眼相关转录因子(MiTF)阳性细胞。我们报告一名48岁男性,其颈部有一个2×3 cm的紫蓝色至色素沉着、不褪色的多边形斑片。组织病理学显示局灶性表皮萎缩、分布不规则的交界性巢以及伴有胶样小体的苔藓样浸润。免疫过氧化物酶研究显示巢内偶尔有全细胞角蛋白和MART-1/黑素-A阳性染色以及局灶性S-100蛋白阳性细胞。重要的是,大多数巢显示大量MiTF和SOX10阳性细胞(每个巢>2个细胞,有些巢大多数细胞阳性)。这种联合染色模式混淆了上述假黑素细胞巢与真正黑素细胞巢之间的免疫组化区分。临床上认为该病变代表单侧扁平苔藓色素沉着症/持久性红斑色素异常而非原位恶性黑色素瘤,此病变突出了临床病理相关性的重要性,并提示在一部分苔藓样皮炎中存在一种新的黑素细胞病变或良性黑素细胞重排的新模式。