北京大学学报(医学版) ›› 2024, Vol. 56 ›› Issue (4): 741-744. doi: 10.19723/j.issn.1671-167X.2024.04.031

• 病例报告 • 上一篇    下一篇

睾丸鞘膜高分化乳头状间皮肿瘤1例

方杨毅1,李强2,黄志高1,陆敏3,洪锴1,张树栋1,*()   

  1. 1. 北京大学第三医院泌尿外科,北京 100191
    2. 北京市中关村医院泌尿外科,北京 100190
    3. 北京大学第三医院病理科,北京 100191
  • 收稿日期:2024-03-18 出版日期:2024-08-18 发布日期:2024-07-23
  • 通讯作者: 张树栋 E-mail:zhangshudong@bjmu.edu.cn

Well-differentiated papillary mesothelial tumour of the tunica vaginalis: A case report

Yangyi FANG1,Qiang LI2,Zhigao HUANG1,Min LU3,Kai HONG1,Shudong ZHANG1,*()   

  1. 1. Department of Urology, Peking University Third Hospital, Beijing 100191, China
    2. Department of Urology, Beijing Zhongguancun Hospital, Beijing 100190, China
    3. Department of Pathology, Peking University Third Hospital, Beijing 100191, China
  • Received:2024-03-18 Online:2024-08-18 Published:2024-07-23
  • Contact: Shudong ZHANG E-mail:zhangshudong@bjmu.edu.cn

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关键词: 间皮肿瘤, 高分化, 乳头状, 睾丸鞘膜, 预后

Abstract:

The mesothelium, which consists of a monolayer of mesothelial cells, extends over the surface of the serosal cavities (pleura, pericardium, peritoneum and tunica vaginalis). Mesothelial tumours of the tunica vaginalis is rare compared with those arise from pleura or peritoneum. According to World Health Organization 2022 Classification of Urinary and Male Genital Tumours (5th edition), mesothelial tumours of the tunica vaginalis were categorized into adenomatoid tumour, well-differentiated papillary mesothelial tumour (WDPMT) and mesothelioma. Since WDPMT of tunica vaginalis was rare, there was no consensus concerning the treatment of it. In this case report, a 29-year-old man who had endured intermittent right scrotal pain for 8 months, aggravating scrotal pain for 2 weeks was admitted. No symptoms, such as frequent, urgent, or painful urination were shown. Physical examination revealed the enlargement and tenderness of right scrotum, with no signs of lifting pain. The most recent scrotal ultrasonography before surgery revealed right hydrocele with maximum depth of 4 centimeters and poor blood flow of right testis. Under the circumstance of patient’ s chronic history of testicular hydrocele, he underwent an emergency operation of right scrotal exploration and hydrocelectomy under epidural anesthesia. After opening the vagina tunic cavity, spot-like bleeding was observed on the right testicle, epididymis and vaginalis surface. The vaginalis was obviously thickened and the inner and outer walls were smooth. The post-operative histopathology revealed a grayish-brown tissue with a thickness of 0.3-0.5 cm, smooth inner and outer walls, and a suspected WDPMT with a diameter of 1. 5 cm. Immunohistochemical staining showed positive for Calretinin, BAP1, WT-1, CK5/6, D2-40 and P16,which confirmed the diagnosis of WDPMT. To sum up, the purpose of this case report was to raise awareness of a rare disease WDPMT, which was usually asymptomatic and could be diagnosed by pathology and immunohistochemistry. The disease should be differentiated from testicular torsion, epididymitis, orchitis and oblique inguinal hernia in symptoms, and from malignant mesothelioma and adenomatoid tumour in pathology. Because of the rarity of the cases, there was no unified standard for the treatment of WDPMT at present. The common treatment methods reported in literature included orchidectomy and vaginectomy. Due to the lack of understanding of this disease, postoperative follow-up was still recommended for at least 5 years.

Key words: Mesothelial tumour, well-differentiated, papillary, Tunica vaginalis, Prognosis

中图分类号: 

  • R737.2

图1

患者术前检查及术中所见"

图2

高分化乳头状间皮肿瘤的形态学特点"

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