Scrotal Wall Metastasis from Adenocarcinoma of Unknown Origin, with Concurrent Extramammary Paget's Disease - a Case Report.

Q3 Medicine
The gulf journal of oncology Pub Date : 2023-09-01
Liang Meng Loy, Kiat Yee Elise Vong, Szu Lyn Cristine Ding, Zhan Peng Daniel Yong, Justin Kwan, Bien Peng Tan
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引用次数: 0

Abstract

Introduction: Scrotal cancer is a very rare disease, with the most common subtype being squamous cell carcinoma. Metastatic carcinoma to the scrotal wall is very rare. A histological finding of adenocarcinoma in a scrotal malignancy invariably suggests a metastasis from another primary cancer. We describe an enigmatic case of metastatic adenocarcinoma to the scrotum managed as metastatic adenocarcinoma of unknown origin. Attempts to identify a primary cancer were complicated by ambiguous diagnostic results. This is the first case in literature of metastatic cancer to the scrotum from an adenocarcinoma of unknown origin, and this was complicated by concurrent extramammary Paget's disease.

Case presentation: A 70-year-old male presented with painless progressive scrotal skin swelling, which was shown on histology to be adenocarcinoma. Immunohistochemistry showed prostatic lineage markers. However, the argument for a prostatic primary was weakened by negative prostate transrectal ultrasound biopsy findings and negative radiological findings. The scrotal metastatic adenocarcinoma was managed as metastatic adenocarcinoma of unknown origin. A differential of occult poorly differentiated prostatic primary was considered in view of the clinical phenotype of an elderly male patient with extensive sclerotic bony metastases, immunohistochemistry results and relatively low PSA level in relation to systemic burden of disease. The patient was managed with palliative systemic chemotherapy (carboplatin/paclitaxel) with initial disease response, but eventually developed progressive disease.

Discussion and conclusion: Finding of adenocarcinoma in scrotal skin malignancy indicates a metastasis and should prompt further work-up to identify a primary cancer, particularly of other genitourinary or lower gastrointestinal origin, so that treatment can be targeted at the underlying primary malignancy. However, attempts to identify a primary cancer might be complicated by ambiguous diagnostic results.

来源不明的腺癌的阴囊壁转移,并发乳腺外Paget病一例报告。
简介:睾丸癌症是一种非常罕见的疾病,最常见的亚型是鳞状细胞癌。阴囊壁转移癌是非常罕见的。阴囊恶性肿瘤中腺癌的组织学发现总是提示来自另一原发性癌症的转移。我们描述了一个神秘的阴囊转移腺癌病例,作为不明来源的转移腺癌处理。鉴别原发性癌症的尝试因不明确的诊断结果而变得复杂。这是文献中第一例不明原因的腺癌转移到阴囊的癌症,并伴有乳腺外Paget病。病例介绍:一名70岁男性,出现无痛性进行性阴囊皮肤肿胀,组织学显示为腺癌。免疫组织化学显示前列腺谱系标记。然而,前列腺经直肠超声活检阴性结果和放射学阴性结果削弱了原发性前列腺的论点。阴囊转移性腺癌被视为来源不明的转移腺癌。考虑到一名患有广泛硬化性骨转移的老年男性患者的临床表型、免疫组织化学结果以及与系统疾病负担相关的相对较低的PSA水平,考虑了隐匿性低分化原发性前列腺的差异。患者接受了姑息性全身化疗(卡铂/紫杉醇),最初有疾病反应,但最终发展为进行性疾病。讨论和结论:阴囊皮肤恶性肿瘤中发现腺癌表明有转移,应促使进一步检查以确定原发性癌症,特别是其他泌尿生殖系统或下消化道来源的癌症,以便针对潜在的原发性恶性肿瘤进行治疗。然而,识别原发性癌症的尝试可能会因诊断结果不明确而变得复杂。
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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来源期刊
The gulf journal of oncology
The gulf journal of oncology Medicine-Medicine (all)
CiteScore
0.90
自引率
0.00%
发文量
37
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