眼睑恶性肿瘤的临床特征和预后:一项五年回顾性研究

Mufid Burgic, Ermina Iljazović, A. Vodenčarević, Musfaha Burgic, Adi Rifatbegović, Amer Mujkanovic, Meliha Halilbašić, Mersiha Sinanovic
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引用次数: 9

摘要

据我们所知,这是第一个关于波黑图兹拉地区眼睑恶性肿瘤的研究,与其他国家的研究结果相似(图兹拉地区每年的眼睑肿瘤发病率约为3.73/10万人口)。眼睑恶性肿瘤相对罕见,但可能致命。然而,如果早期发现并适当治疗,预后通常很好。目的:对眼睑恶性肿瘤患者的临床及显微分析,提出眼睑恶性肿瘤的手术治疗方法及重建方法。方法:回顾性研究2012年1月至2016年12月在图兹拉大学临床中心接受手术治疗的60例眼睑恶性肿瘤患者,根据切除病变的最终组织学检查结果初步诊断为眼睑恶性肿瘤。结果:恶性肿瘤组中以基底细胞癌(BCC)最为常见(85%),主要发生在下眼睑(92.16%),女性居多(51.06%)。鳞状细胞癌(SCC)是第二常见的眼睑恶性肿瘤(15%),并倾向于累及下眼睑,男性居多(55.56%)。肿瘤直径达2cm(临床T1期)占78.33%,其中根治性切除占95.74%,非根治性切除占4.26%。结论:组织学证实肿瘤清除后,建议采用完全切除治疗。神经周围扩散是一个不良的预后征象,可能需要术后放疗。眼眶侵犯是一种罕见的并发症,但如果及早发现,可以通过清除术有效治疗。由于表现多样,准确诊断需要组织学检查,任何可疑的眼睑病变都应切除或活检。所有恶性肿瘤患者应被告知复发或新发肿瘤的风险,并鼓励参加终身随访。
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Clinical Characteristics and Outcome of Malignant Eyelid Tumors: A Five-Year Retrospective Study
Introduction: To the best of our knowledge, this is the first study about malignant eyelid tumors in the region of Tuzla, Bosnia and Herzegovina, and it shows similar results comparing with other countries (the annual incidence of eyelid tumors in Tuzla region is about 3.73/100 000 population). Malignant eyelid tumors are relatively uncommon, but potentially fatal disease. However, if detected early and treated adequately, the prognosis is generally excellent. Aim: The aim of this study was the clinical and microscopical analysis of malignant eyelid tumors in treated patients, the presentation of surgical treatment and reconstructive methods of eyelid tumors. Methods: This retrospective study included 60 patients surgically treated at the University Clinical Center Tuzla from January 2012 to December 2016, who were initially diagnosed with malignant eyelid tumors in accordance to the final results obtained by histological examination of excised lesions. Results: In the group of malignant tumors, the most common tumors were BCC (85%), which were predominantly found on the lower eyelids (92.16%) and showed female predominance (51.06%). SCC was the second most common eyelid malignancy (15%) and showed a predilection for the lower eyelid involvement and male predominance (55.56%). Tumors up to 2 cm in diameter (clinical stage T1) were found in 78.33% of cases, 95.74% of which with radical excision, while 4.26% with non-radical excision. Conclusion: Treatment by complete excision with histological confirmation of tumor clearance is recommended. Perineural spread is an adverse prognostic sign, which may require postoperative radiotherapy. Orbital invasion is a rare complication but, if recognized early, it can be treated effectively with exenteration. Because presentation varies and histological examination is required for accurate diagnosis, any suspicious lesion occurring on the eyelids should be excised or biopsied. All patients with malignant tumors should be advised of the risk of recurrent or new tumors and encouraged to attend lifelong follow up.
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