Voigt J J, Alsaati T, Gorguet B, Caveriviere P, Scarna H, Bugat R, Delsol G
Ann Pathol. 1985;5(3):195-203.
The clinical and pathological features of 14 cases of Merkel cell carcinoma are reported. They commonly arise in the skin of elderly patients, particularly on the face and pelvis. They have a loco-regional aggressivity (nodal metastases in 4 cases) but some patients die with disseminated metastases (2 cases). These tumors are composed of round cells with scanty cytoplasm, arranged in solid or trabecular sheets. Mitotic figures are usually numerous. The ultrastructural study reveal secretory granules and paranuclear collection of intermediate filaments. Immunohistochemical phenotype is highly characteristic: cytoplasmic diffuse positivity with an anti-neuron-specific enolase polyclonal antibody; polar and/or diffuse positivity with anti-cytokeratin, anti-epithelial membrane antigen and anti-S100 protein monoclonal antibodies; polar positivity with an anti-neurofilament monoclonal antibody. The negativity with an anti-common leucocyte antigen monoclonal antibody is helpful to differentiate Merkel cell carcinoma from cutaneous malignant lymphoma.
报告了14例默克尔细胞癌的临床和病理特征。它们通常发生于老年患者的皮肤,尤其是面部和骨盆。这些肿瘤具有局部侵袭性(4例出现淋巴结转移),但有些患者死于远处转移(2例)。这些肿瘤由胞质稀少的圆形细胞组成,呈实性或小梁状排列。核分裂象通常较多。超微结构研究显示有分泌颗粒和中间丝的核旁聚集。免疫组化表型具有高度特征性:抗神经元特异性烯醇化酶多克隆抗体呈胞质弥漫阳性;抗细胞角蛋白、抗上皮膜抗原和抗S100蛋白单克隆抗体呈极性和/或弥漫阳性;抗神经丝单克隆抗体呈极性阳性。抗普通白细胞抗原单克隆抗体阴性有助于将默克尔细胞癌与皮肤恶性淋巴瘤相鉴别。