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Carcinoma ex benign pleomorphic adenoma of the parotid gland.

机译:腮腺良性多形性腺癌。

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摘要

BACKGROUND: Carcinoma in pleomorphic salivary adenoma is a common histologic subtype of primary parotid malignancy. METHODS: In this study, 28 patients (predominantly male) with histologically diagnosed carcinoma in pleomorphic salivary adenoma presenting over 10 years were retrospectively reviewed. RESULTS: Only 25 percent of patients had a previously treated pleomorphic salivary adenoma. Although the presenting features suggested malignancy in some cases, overall they were nonspecific, overlapping with the presentation of benign disease. Preoperative investigations included fine needle aspiration cytology, which was only 29-percent sensitive, and computed tomography and/or magnetic resonance imaging. There were 14 superficial and 12 total or radical parotidectomies. The facial nerve was resected en bloc with the tumor in nine cases and immediately reconstructed with good reanimation results in patients with recent-onset facial paresis. Only 44 percent of patients had a complete histologic tumor clearance, and this was the most significant determinant of survival (p < 0.01, log-rank analysis). The locoregional control rate was 66 percent at 5 years, but recurrent disease proved invariably fatal. Five-year disease-specific survival was 44 percent with a high rate of disease-specific mortality (87 percent). CONCLUSIONS: Carcinoma in pleomorphic salivary adenoma is very difficult to diagnose preoperatively. Fine needle aspiration cytology had a disappointingly low sensitivity for this tumor, potentially misdirecting surgical management. While good locoregional disease control could be achieved with surgery and radiotherapy, carcinoma in pleomorphic salivary adenoma was shown to be aggressive with a high disease-specific rate of mortality. Given that incomplete tumor resection was the most important prognostic factor, a high index of clinical suspicion, radical ablative surgery, and immediate soft-tissue and nerve reconstruction for proven cases are advocated.
机译:背景:多形性涎腺腺癌是原发性腮腺恶性肿瘤的常见组织学亚型。方法:本研究回顾性分析了10年来出现的多形性涎腺腺瘤组织学诊断为癌的28例患者(主要为男性)。结果:只有25%的患者曾接受过多形性涎腺腺瘤治疗。尽管呈现的特征提示在某些情况下为恶性肿瘤,但总体而言它们是非特异性的,与良性疾病的呈现重叠。术前检查包括敏感度仅为29%的细针穿刺细胞学检查,计算机断层扫描和/或磁共振成像。有14例浅表和12例完全或根治性腮腺切开术。面部神经与肿瘤整块切除,其中9例在近期发生面部轻瘫的患者中立即重建,并具有良好的复活效果。只有44%的患者具有完整的组织学肿瘤清除率,这是存活率的最重要决定因素(p <0.01,对数秩分析)。 5年局部控制率为66%,但反复发作的疾病始终被证明是致命的。五年特定疾病生存率为44%,特定疾病死亡率较高(87%)。结论:多形性涎腺腺癌在术前很难诊断。细针穿刺细胞学检查对该肿瘤的敏感性低得令人失望,可能会误导外科治疗。尽管可以通过手术和放疗实现对局部区域疾病的良好控制,但多形性涎腺腺瘤中的癌仍具有侵袭性,且病死率高。鉴于不完整的肿瘤切除是最重要的预后因素,因此提倡对可疑病例进行高度的临床怀疑,根治性消融手术以及立即进行软组织和神经重建。

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