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Merkel细胞癌(Merkel cell carcinoma,MCC)是一种临床罕见的高度恶性神经内分泌肿瘤,具有较强的侵袭性[1]。1972年Toker[2]首次以皮肤梁状癌报道,之后的大量研究证实了这种皮肤肿瘤来源于Merkel细胞,并具有神经内分泌功能。本文就本院诊治的1例皮肤Merkel细胞癌报告如下。临床资料患者,女性,52岁。主因右颞部肿物6个月,于2014年10月就诊。6个月前无明显诱因,患者右颞部出现一米粒大小灰白色肿物,略隆起,有轻度痒感。自行涂抹鱼石脂软膏,无效,肿物逐渐增大。平素体健,家族中
Merkel cell carcinoma (Merkel cell carcinoma, MCC) is a clinically rare high-grade neuroendocrine tumor with high invasiveness [1]. In 1972, Toker [2] first reported as a skin-beam carcinoma. Subsequent studies confirmed that this dermal tumor originated from Merkel cells and possessed neuroendocrine function. This article on the diagnosis and treatment of a hospital skin Merkel cell carcinoma is as follows. Clinical data Patient, female, 52 years old. Main due to right temporal tumor for 6 months, in October 2014 treatment. 6 months ago, no obvious incentive, the patient appeared in the right temporal part of the size of a grain of gray-white tumor, slightly uplift, mild itching. Fish grease ointment coated, invalid, the tumor gradually increased. Usually physical health, family