A Case of Combined Germ Cell Tumor in Testis

고환의 원발성 결합성 생식세포 종양 -A case report with literature review-

  • Nam, Hae-Joo (Department of Anatomical Pathology College of Medicine, Yeungnam University) ;
  • Choi, Won-Hee (Department of Anatomical Pathology College of Medicine, Yeungnam University) ;
  • Lee, Tae-Sook (Department of Anatomical Pathology College of Medicine, Yeungnam University) ;
  • Suh, Jun-Gju (Department of Urology College of Medicine, Yeungnam University) ;
  • Lee, Kyung-Chul (Laboratory Service, VA Medical Center)
  • 남혜주 (영남대학교 의과대학 병리학교실) ;
  • 최원희 (영남대학교 의과대학 병리학교실) ;
  • 이태숙 (영남대학교 의과대학 병리학교실) ;
  • 서준규 (영남대학교 의과대학 비뇨기과학교실) ;
  • 이경철
  • Published : 1985.06.30

Abstract

Primary germ cell tumor of the testis is, rare, which occupies 1 to 2% of all reported malignant male neoplasms. Combined primary germ ceil tumor of the testis composed of embryonal carcinoma and seminoma is more rare tumor. The authors experienced a case of 50-year old male who presented with painless enlargement of right testicle. He has had radical orchiectomy and diagnosed by pathologically as combined germ cell tumor of testis. The testicle is measuring 180 gm in weight and $9{\times}6{\times}5$ cm in dimension, and almostly replaced by tumor mass. Grossly the tumor is rubbery solid smooth tumor mass, with variegated cut surface with geographically outlined diffuse necrotic area. Histologically the tumor is composed of two components of tumor, which are solid growth pattern of large round to polyhedral cells with clear or granular cytoplasm and distinct cell border, and anastomosing glandular and papillary arrangement of anaplastic epithelial cells. The former corresponds to seminoma, and the latter to embryonal carcinoma. Each tumor lobule is separated by abundant fibrous stroma.

저자들은 최근 50세 남자 환자에서 병리조직학적으로 증명된 정상피종과 태아성 암으로 구성된 결합종양 1예를 경험하였기에 문헌 고찰과 아울러 보고하는 바이다.

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