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Pigmented adenoid cystic carcinoma of the ear skin arising from the epidermis: a case report with immunohistochemical studies

机译:表皮色素性腺样囊性囊性癌:免疫组化研究1例

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摘要

Adenoid cystic carcinoma (ACC) in the skin is very rare; only about 60 cases have been reported. Herein presented is a case of pigmented ACC arising from epidermis of the ear skin. An 85-year-old man presented black tumor of the right ear. Dermatologists’ diagnosis was basal cell carcinoma (BCC). Large biopsy was obtained. The biopsy showed proliferation of atypical basaloid cells arranged in a cribriform pattern. The tumor cells were continuous with epidermis, as if it arose from the epidermis. Focal areas show melanin deposition in the tumor cells. Mucin stains showed that the tumor cells and tubular lumens contained acidic mucin. Immunohistochemically, the tumor cells were positive for cytokeratin (CK) AE1/3, CK34BE12, CK5/6, CK7, CK14, p63, alpha-smooth muscle actin (ASMA), S100 protein, p53, Ki-67 (labeling 85%), KIT, PDGFRA and CD56. The tumor cells were negative for CK CAM5.2, CK8, CK18, CK19, CK20, EMA, desmin, CEA, HMB45, CD10, CD34, neuron-specific enolase, chromogranin, synaptophysin, CDX2, MUC1, MUC2, MUC5AC and MUC6. HMB-positive and S100-positive melanocytes were seen in a very few areas. Since characteristic cribriform pattern was recognized in the tumor and the tumor showed epithelial markers, myoepithelial markers (CD14, p63, ASMA, S100 protein) and KIT, the pathological diagnosis of ACC was made. No distant and lymph node metastasis is now seen. The patient will be treated by complete resection. The present cutaneous ACC was unique in that the ACC arose from the epidermis, had melanin pigment, and occurred in ear skin.
机译:皮肤腺样囊性癌(ACC)非常罕见;仅报道了60例。本文介绍的是一例从耳朵皮肤表皮产生的色素沉着的ACC。一名85岁的男子出现右耳黑色瘤。皮肤科医生的诊断是基底细胞癌(BCC)。大活检。活检显示以筛状排列的非典型基底细胞增生。肿瘤细胞与表皮是连续的,好像它是由表皮产生的。病灶区域显示黑色素沉积在肿瘤细胞中。粘蛋白染色表明,肿瘤细胞和肾小管腔中含有酸性粘蛋白。免疫组织化学分析,肿瘤细胞的细胞角蛋白(CK)AE1 / 3,CK34BE12,CK5 / 6,CK7,CK14,p63,α平滑肌肌动蛋白(ASMA),S100蛋白,p53,Ki-67呈阳性(标记为85%) ,KIT,PDGFRA和CD56。肿瘤细胞对CK CAM5.2,CK8,CK18,CK19,CK20,EMA,结蛋白,CEA,HMB45,CD10,CD34,神经元特异性烯醇化酶,嗜铬粒蛋白,突触素,CDX2,MUC1,MUC2,MUC5AC和MUC6呈阴性。 HMB阳性和S100阳性黑色素细胞出现在极少数区域。由于在肿瘤中识别出特征性的筛状图案,并且肿瘤表现出上皮标志物,肌上皮标志物(CD14,p63,ASMA,S100蛋白)和KIT,因此对ACC进行了病理诊断。现在没有远处和淋巴结转移。将通过完全切除治疗该患者。本发明的皮肤ACC的独特之处在于,ACC来自表皮,具有黑色素色素,并发生在耳部皮肤中。

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