Serie de casos : Características del Carcinoma de Células de Merkel en pacientes del Centro de Cáncer de Piel del Hospital Italiano de Buenos Aires - Argentina. 2004-2018

Juan Pablo Valdivieso Aguirre, Mercedes Solis Ramirez, Amalia Luna, Damián Ferrario, L. Mazzuoccolo
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Abstract

BACKGROUND: Merkel cell carcinoma is described as a malignant and aggressive neuroendocrine tumor, which represents less than 1% of non-melanoma skin tumors. It is a rare type of skin cancer that is associated with a poor prognosis and a high rate of recurrence. Despite significant advances, its pathogenesis is still poorly understood. Early diagnosis and proper management are essential to improve the survival rate. Although it affects both genders, it has male predominance. It is presented as hard, bright, reddish, and asymptomatic tumors with a certain predilection for head, neck and limbs. The treatment is surgical and in some cases, it requires adjuvant radiation therapy. An early diagnosis and appropriate handling are essential to improve the survival rate. METHODS: We conducted an observational, descriptive study ⸻case series⸻, which included 10 patients diagnosed with MCC, from the dermatology service of the Skin Cancer Center of Hospital Italiano de Buenos Aires, from January 2004 to August 2018. RESULTS: Over the course of 15 years, ten patients, 5 men and 5 women, were clinically and histopathologicallly diagnosed with Merkel Cell Carcinoma, with mean age of presentation of 83 years (range: 74-95 years). There was a high frequency (70%) of immunological alterations due to autoimmune diseases, renal-transplanted patients, and chronic lymphocytic leukemia. The therapeutic option was conventional surgery, with a margin of 3 cm, in six patients and Mohs micrographic surgery in four patients. Three patients developed local recurrence, who received adjuvant radiotherapy. CONCLUSION: The mean age of presentation was 83 years of age; there was no predominance according to sex. Most cases were localized in head and neck. Most of the patients had a concomitant immunological alteration. Most cases were resolved by conventional surgery. Recurrence rate was lower than expected (30%).
病例系列:2004-2018年阿根廷布宜诺斯艾利斯意大利医院皮肤癌中心默克尔细胞癌患者特征
背景:默克尔细胞癌是一种恶性侵袭性神经内分泌肿瘤,占非黑色素瘤皮肤肿瘤的不到1%。这是一种罕见的皮肤癌,预后差,复发率高。尽管取得了重大进展,但其发病机制仍知之甚少。早期诊断和适当的治疗是提高生存率的关键。虽然它影响两性,但以男性为主。它表现为硬、亮、红、无症状的肿瘤,有一定的头部、颈部和四肢的偏好。治疗方法是手术,在某些情况下,需要辅助放射治疗。早期诊断和适当处理对提高生存率至关重要。方法:我们进行了一项观察性描述性研究⸻病例系列⸻,其中包括2004年1月至2018年8月期间来自布宜诺斯艾利斯意大利医院皮肤癌中心皮肤科服务的10例诊断为MCC的患者。结果:在15年的时间里,10例患者,5男5女,临床和组织病理学诊断为默克尔细胞癌,平均年龄为83岁(范围:74-95岁)。免疫性疾病、肾移植患者和慢性淋巴细胞白血病引起的免疫改变发生率很高(70%)。6例患者的治疗选择为常规手术,切缘为3cm, 4例患者采用莫氏显微摄影手术。3例局部复发,均行辅助放疗。结论:患者的平均发病年龄为83岁;没有性别上的优势。多数病例局限于头颈部。大多数患者伴有免疫改变。大多数病例通过常规手术解决。复发率低于预期(30%)。
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