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头颈部黏膜黑色素瘤

Mucosal melanoma of the head and neck.

作者信息

Kanetaka Sayaka, Tsukuda Mamoru, Takahashi Masahiro, Komatsu Masanori, Niho Tatsuo, Horiuchi Choichi, Matsuda Hideki

机构信息

Department of Otolaryngology, Head and Neck Surgery, Yokohama City University School of Medicine, Kanagawa 236-0004, Japan.

出版信息

Exp Ther Med. 2011 Sep;2(5):907-910. doi: 10.3892/etm.2011.313. Epub 2011 Jun 30.

Abstract

Mucosal melanoma of the head and neck (MMHN) is a rare malignant tumor associated with a poor prognosis. A retrospective study of case records of patients treated at our department between 1992 and 2010 was carried out. Thirteen patients were enrolled. The median age of the patients (3 males and 10 females) was 61 years (range 39-78). The median follow-up period was 48 months (range 10-115). Two common primary sites were the nasal cavity (8 cases) and sinonasal complex (5 cases). Ten patients (77%) received curative surgery. Chemotherapy was administered to 10 patients. In addition, lymphokine-activated killer (LAK) cell therapy was administered to 7 patients as adjunctive immunotherapy after the initial treatment course. The overall 5-year, cause-specific survival rate was 56%. Patients who received adjunctive LAK cell therapy had a survival rate of 67% at 5 years, while patients who did not receive adjunctive LAK cell treatment had a survival rate of 33%. MMHN is associated with a poor survival rate. The most common cause of death is distant metastasis. Surgery, radiotherapy and chemotherapy are common strategies for MMHN, but the control of metastasis is difficult. The use of immunotherapy remains uncommon for MMHN. However, from the viewpoint of a systemic disease, due to its high rate of metastases, immunotherapy using LAK cell treatment may contribute to the improvement of prognosis in patients with MMHN.

摘要

头颈部黏膜黑色素瘤(MMHN)是一种罕见的恶性肿瘤,预后较差。我们对1992年至2010年在我科接受治疗的患者病历进行了回顾性研究。共纳入13例患者。患者(3例男性和10例女性)的中位年龄为61岁(范围39 - 78岁)。中位随访期为48个月(范围10 - 115个月)。两个常见的原发部位是鼻腔(8例)和鼻窦复合体(5例)。10例患者(77%)接受了根治性手术。10例患者接受了化疗。此外,7例患者在初始治疗疗程后接受了淋巴因子激活的杀伤(LAK)细胞治疗作为辅助免疫治疗。总体5年病因特异性生存率为56%。接受辅助LAK细胞治疗的患者5年生存率为67%,而未接受辅助LAK细胞治疗的患者生存率为33%。MMHN的生存率较差。最常见的死亡原因是远处转移。手术、放疗和化疗是MMHN的常见治疗策略,但转移的控制较为困难。免疫治疗在MMHN中的应用仍然不常见。然而,从全身性疾病的角度来看,由于其转移率高,使用LAK细胞治疗的免疫治疗可能有助于改善MMHN患者的预后。

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