Medicine School Department of Federal University of Fronteira Sul - UFFS, Chapecó City 89815-899, Brasil.
Exp Oncol. 2022 Aug;44(2):174-176. doi: 10.32471/exp-oncology.2312-8852.vol-44-no-2.18006.
Primary cystic adenoid skin carcinoma is a rare and poorly documented neoplasm in literature worldwide, with just over 250 reports. This work describes a 52-year-old male patient, with no comorbidities, who presented this neoplasm in nodular format in the posterior thoracic region, associated with localized pain and erythema - symptoms that led him to seek medical help. The clinical findings, differential diagnosis and treatment particularities were reviewed and correlated with the clinical case. The choice of type of surgical treatment was done considering the characteristics of the primary lesion that are associated with a worse prognosis. Despite its rarity, this neoplasm is easily identified through histological examination, the correct choice of treatment and patient follow-up, essential to increase survival. Thus, this work contributes to diminish the scarcity of literature related to this topic, especially the form of treatment employed.
原发性囊性腺样皮肤癌是一种罕见且在世界范围内文献记录甚少的肿瘤，仅有超过 250 例报告。本工作描述了一名 52 岁男性患者，无合并症，在后胸区域呈结节状出现这种肿瘤，伴有局部疼痛和红斑 - 这些症状导致他寻求医疗帮助。回顾了临床发现、鉴别诊断和治疗特点，并与临床病例相关联。选择手术治疗类型时考虑了与预后较差相关的原发性病变的特征。尽管这种肿瘤很少见，但通过组织学检查很容易识别，正确的治疗选择和患者随访对于提高生存率至关重要。因此，本工作有助于减少与该主题相关的文献稀缺性，特别是所采用的治疗方法。
