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首页> 外文期刊>Archivio Italiano di Urologia e Andrologia >Metastasis of the epididymis and spermatic cord from pancreatic adenocarcinoma: A rare entity. Description of a case and revision of literature
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Metastasis of the epididymis and spermatic cord from pancreatic adenocarcinoma: A rare entity. Description of a case and revision of literature

机译:胰腺腺癌附睾和精索的转移:一种罕见的实体。案例描述和文献修订

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Introduction: Metastatic epididymal and spermatic cord adenocarcinoma from epithelial tumors are a rare condition. The most frequent primary cancers are prostate, lung, kidney, gastrointestinal tumors and breast. In literature, there are very low number of cases reporting metastasis from pancreatic cancer to epididymis and spermatic cord. Case description: We report a case of 70-years old man with history of left orchiectomy for undescended testicle, who presented to our department with a palpable nodule in the right scrotum. Scrotal ultrasound revealed an inhomogeneous hypoechoic nodule of epididymis and/or spermatic cord. Neoplastic markers showed high levels of CEA (carcinoembryonic antigen) and bHCG (beta Human Chorionic Gonadotropin). The patient underwent right surgical scrotal exploration with orchifunicolectomy. Pathologic examination revealed pathologic tissue showing rare glandular structures. Immunohistochemistry profile was compatible with malign epithelial neoplasm with glandular differentiation. Total body CT-scan revealed pathologic tissue in pancreas between head and body and a suspect pathologic lesion in liver and 18-FDG PET-scan confirmed the pancreatic neoplastic mass and a suspect secondary hepatic lesion. Biopsy of pancreatic pathologic area was positive for ductal pancreatic adenocarcinoma. The patient was sent to oncologic evaluation and started chemotherapy. Conclusions: Malignancies of epididymis and spermatic cord are rare entities and, in literature, very low number of cases of metastasis from pancreatic carcinoma to epididymis and spermatic cord are described. Early differential diagnosis is fundamental mostly in those patients with age range unusual for testis cancers.
机译:简介:上皮肿瘤转移的附睾和精索腺癌是一种罕见的疾病。最常见的原发癌是前列腺癌,肺癌,肾癌,胃肠道肿瘤和乳腺癌。在文献中,极少数病例报告了从胰腺癌转移至附睾和精索的转移。病例描述:我们报告一例70岁的男性,睾丸未降,有左睾丸切除术史,他向我们科室提出了位于右阴囊的明显结节。阴囊超声显示附睾和/或精索的异质性低回声结节。肿瘤标记物显示高水平的CEA(癌胚抗原)和bHCG(β人绒毛膜促性腺激素)。该患者接受了睾丸切除术并进行了阴囊探查。病理检查发现病理组织显示稀有的腺体结构。免疫组织化学谱与具有腺分化的恶性上皮肿瘤相容。全身CT扫描显示头部和身体之间的胰腺中有病理组织,肝脏中有可疑的病理病变,而18-FDG PET扫描证实了胰腺肿瘤性肿块和疑似继发性肝病变。胰管腺癌的病理切片活检为阳性。患者被送去进行肿瘤评估并开始化疗。结论:附睾和精索的恶性肿瘤是罕见的,在文献中,从胰腺癌到附睾和精索的转移病例很少。早期鉴别诊断主要是针对那些睾丸癌罕见的年龄范围的患者。

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