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头颈部默克尔细胞癌的腮腺转移:14例病例系列

Parotid gland metastasis in Merkel cell carcinoma of the head and neck: A series of 14 cases.

作者信息

Day Kristine E, Carroll William R, Rosenthal Eben L

机构信息

Department of Otolaryngology, UAB School of Medicine, BDB Suite 563, 1808 7th Ave. S., Birmingham, AL 35294-0012, USA.

出版信息

Ear Nose Throat J. 2016 Sep;95(9):398-404.

Abstract

Merkel cell carcinoma (MCC) is a rare cutaneous cancer of neuroendocrine cell origin that occurs frequently on the head and neck. With a high incidence of local recurrence and regional and distant metastasis, it carries a poor prognosis. We performed a retrospective study to determine the prognostic implications of parotid gland metastasis in MCC of the head and neck. Our study population was made up of 14 patients-13 men and 1 woman, aged 62 to 87 years (mean: 75.9)-who underwent a parotidectomy for the diagnosis of MCC over a period of 10 years and 9 months. Ten patients had a primary skin lesion of the head and neck and 4 presented with a parotid mass and an unknown primary. In all, 13 of the 14 patients were found to have parotid involvement-either a direct extension of MCC into the gland or a positive intraparotid lymph node; some patients had both. All patients underwent tumor excision, and 10 underwent neck dissection. Eleven patients received adjuvant radiotherapy; none received adjuvant chemotherapy. Of the 10 patients who underwent a neck dissection, 6 were found to have a cervical lymph node metastasis on pathologic examination. Follow-up ranged from 1.3 to 39.2 months (mean: 12.4). Three patients were lost to follow-up shortly after surgery, although some information was available on 2 of them. At the final follow-up, mortality data were available on 12 patients; of these, 11 had died. The lone survivor was the patient without a parotid metastasis. Among those known to have died, survival ranged from 1.6 to 49.2 months (mean: 16.0). We conclude that parotid metastasis in patients with MCC of the head and neck is associated with a dismal survival rate that is even worse than the poor survival associated with cervical node involvement.

摘要

默克尔细胞癌(MCC)是一种起源于神经内分泌细胞的罕见皮肤癌,常见于头颈部。由于局部复发、区域及远处转移的发生率较高,其预后较差。我们进行了一项回顾性研究,以确定腮腺转移对头颈部MCC预后的影响。我们的研究对象包括14例患者,其中13例男性和1例女性,年龄在62至87岁之间(平均75.9岁),他们在10年9个月的时间里因诊断为MCC而接受了腮腺切除术。10例患者头颈部有原发性皮肤病变,4例表现为腮腺肿块且原发灶不明。14例患者中,共有13例发现有腮腺受累,即MCC直接蔓延至腮腺或腮腺内淋巴结阳性;部分患者两者均有。所有患者均接受了肿瘤切除,10例患者接受了颈部清扫术。11例患者接受了辅助放疗;无人接受辅助化疗。在接受颈部清扫术的10例患者中,6例经病理检查发现有颈部淋巴结转移。随访时间为1.3至39.2个月(平均12.4个月)。3例患者术后不久失访,不过其中2例有一些可用信息。在最后一次随访时,有12例患者的死亡数据;其中11例已死亡。唯一的幸存者是没有腮腺转移的患者。在已知死亡的患者中,生存期为1.6至49.2个月(平均16.0个月)。我们得出结论,头颈部MCC患者的腮腺转移与生存率极低相关,甚至比颈部淋巴结受累相关的不良生存情况更差。

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