眼睑梅克尔细胞癌。

IF 1.3 Q4 ONCOLOGY
ecancermedicalscience Pub Date : 2025-07-17 eCollection Date: 2025-01-01 DOI:10.3332/ecancer.2025.1946
Dario Alvaro Rueda, Cecilia Schweitzer, Lorena Di Nisio, María Laura Piccoletti, Nicolas Torressi, Víctor Acevedo, Silvia Ferrandini
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引用次数: 0

摘要

默克尔细胞癌(MCC)是一种罕见的侵袭性皮肤肿瘤,其特点是局部复发率高,淋巴结受累。我们提出的情况下,58岁的妇女谁发展了一个5厘米的肿瘤右下眼睑,导致眼闭塞。磁共振成像显示右眼眶外生性病变,活检证实了MCC的诊断。在手术切除和宫颈排空后,患者接受辅助放疗。最终诊断为MCC, pT3期pN1 M0。眼周位置和肿瘤大小是决定治疗的决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bulky palpebral Merkel cell carcinoma of the eyelid.

Bulky palpebral Merkel cell carcinoma of the eyelid.

Bulky palpebral Merkel cell carcinoma of the eyelid.

Bulky palpebral Merkel cell carcinoma of the eyelid.

Merkel cell carcinoma (MCC) is a rare and aggressive tumour of the skin, characterised by a high rate of local recurrence and lymph node involvement. We present the case of a 58-year-old woman who developed a 5-cm tumour on the right lower eyelid, leading to ocular occlusion. Magnetic resonance imaging revealed an exophytic lesion in the right orbit, and a biopsy confirmed the diagnosis of MCC. After complete surgical resection and cervical emptying, the patient was treated with adjuvant radiotherapy. The final diagnosis was MCC, stage pT3 pN1 M0. The periocular location and tumour size were determinants in the treatment decision.

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来源期刊
CiteScore
3.80
自引率
5.60%
发文量
138
审稿时长
27 weeks
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