Primary Cutaneous Adenoid Cystic Carcinoma Of The Chest Wall With Axillary Lymph Node Metastases And Its Management: A Case Report.

Klein Dantis, Radhakrishna Ramchandani, Shamendra Anand Sahu, Vandita Yogendra Singh, Subhajit Dasgupta
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Abstract

Primary cutaneous adenoid cystic carcinoma (PCACC) is a rare form of adenoid cystic carcinoma (ACC) arising commonly from the salivary gland. Less often they originate outside the head and neck region, with the scalp being the commonest cutaneous site in 40% of the cases. The presentation on the chest wall is rare, with no reports to date on axillary lymph node metastases. Here we report a case of a 65-year-old female with previously operated PCACC of the chest wall at a different center, showing uptake on positron emission tomography imaging at the site of surgical scar that w as inconclusive on needle biopsy metastasized to the axillary lymph node confirmed by needle biopsy managed with wide local excision, axillary lymph node dissection, and chest wall reconstruction with keystone island flap. The postoperative outcome was uneventful with no recurrence or axillary complications at one year's follow-up. She was advised to receive adjuvant radiotherapy; however, she refused. To conclude, though PCACC is rare, they can have an aggressive presentation, and a multidisciplinary approach is necessary for a better outcome.

原发性胸壁皮肤腺样囊性癌伴腋窝淋巴结转移及其处理一例报告。
原发性皮肤腺样囊性癌(PCACC)是一种罕见的腺样囊性癌(ACC),常见于唾液腺。很少发源于头颈部以外,40%的病例发源于最常见的皮肤部位头皮。在胸壁的表现是罕见的,没有报告到目前为止腋窝淋巴结转移。在此,我们报告一例65岁女性胸壁不同中心的PCACC患者,在手术疤痕部位的正电子发射断层成像显示,针活检不确定的手术疤痕转移到腋窝淋巴结,经针活检证实,局部广泛切除,腋窝淋巴结清扫,胸壁重建keystone岛状皮瓣。术后随访1年无复发或腋窝并发症。建议行辅助放疗;然而,她拒绝了。总之,虽然PCACC是罕见的,但它们可以有侵略性的表现,为了更好的结果,多学科的方法是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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