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原发性交界性黏液性睾丸肿瘤:一例报告及文献综述

Primary Borderline Mucinous Testicular Tumor: A Case Report and Literature Review.

作者信息

Hao Changjuan, Kang Chunsong, Kang Xiaoyan, Yu Zhuanzhuan, Li Tingting, Xue Jiping

机构信息

Department of Ultrasound, Shanxi Bethune Hospital affiliated to Shanxi Medical University, Taiyuan, China.

Department of Pathology, Shanxi Bethune Hospital affiliated to Shanxi Medical University, Taiyuan, China.

出版信息

Front Oncol. 2021 Mar 9;10:619774. doi: 10.3389/fonc.2020.619774. eCollection 2020.

Abstract

Primary mucinous tumors of the testis and paratestis are very rare, with only 29 reported cases detected in a PubMed search. The histopathological characteristics of primary testicular mucinous tumors are similar to their ovarian counterparts, and the diagnosis and naming criteria refer to the criteria for female ovarian mucinous tumors. However, the clinical and imaging features of primary testicular mucinous tumors are poorly understood, and they are thus frequently undiagnosed or misdiagnosed. We present the case of a patient with a primary testicular mucinous tumor. A 52-year-old man presented with a 1-year history of painless enlargement of the left scrotum. Ultrasound examination revealed a cystic mass in the left testis, with viscous fluid areas and calcified spots, irregular solid bulges on the cyst wall, and a small blood supply. Serum alpha-fetoprotein, β-human chorionic gonadotropin, lactate dehydrogenase, renal function, inflammatory markers, and routine urine and blood examinations were all normal. The patient underwent radical resection of the left testis. Postoperative pathology showed a multilocular cystic mass, with the inner wall of the sac lined with mucous columnar epithelial cells, some with mild nuclear atypia, and no interstitial infiltration. The pathological diagnosis was testicular mucinous tumor. Postoperative abdominal and pelvic computed tomography, colonoscopy, and gastroscopy showed no suspicious lesions. The final diagnosis was primary testicular borderline mucinous tumor. The patient underwent postoperative follow-up examinations once a year for 4 years. Serum tumor markers, scrotal ultrasound, abdominal and pelvic computed tomography scans, and colonoscopy and gastroscopy revealed no evidence of metastases or other primary adenocarcinoma. This case highlights the clinical and imaging characteristics of primary testicular mucinous tumors, which might aid their differential diagnosis.

摘要

睾丸及睾丸旁原发性黏液性肿瘤极为罕见,在PubMed检索中仅发现29例报道病例。原发性睾丸黏液性肿瘤的组织病理学特征与其卵巢对应肿瘤相似,诊断及命名标准参照女性卵巢黏液性肿瘤的标准。然而,原发性睾丸黏液性肿瘤的临床及影像学特征尚不清楚,因此常未被诊断或误诊。我们报告一例原发性睾丸黏液性肿瘤患者的病例。一名52岁男性,左侧阴囊无痛性肿大1年。超声检查显示左侧睾丸有一囊性肿物,内有黏性液体区及钙化斑,囊壁有不规则实性凸起,血供少。血清甲胎蛋白、β-人绒毛膜促性腺激素、乳酸脱氢酶、肾功能、炎症标志物以及尿常规和血常规检查均正常。患者接受了左侧睾丸根治性切除术。术后病理显示为多房囊性肿物,囊内壁衬有黏液柱状上皮细胞,部分有轻度核异型性,无间质浸润。病理诊断为睾丸黏液性肿瘤。术后腹部及盆腔计算机断层扫描、结肠镜检查及胃镜检查均未发现可疑病变。最终诊断为原发性睾丸交界性黏液性肿瘤。患者术后每年进行随访检查,共4年。血清肿瘤标志物、阴囊超声、腹部及盆腔计算机断层扫描以及结肠镜检查和胃镜检查均未发现转移或其他原发性腺癌的证据。该病例突出了原发性睾丸黏液性肿瘤的临床及影像学特征,可能有助于其鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20c/7986722/67f0a8b3384a/fonc-10-619774-g001.jpg

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