Bilateral Testicular Epidermoid Cysts in a Man with Klinefelter Syndrome: A Case Report

被引:1
作者
Win, Mya L. [1 ]
Kaur, Devinder [1 ]
Oyibo, Samson O. [1 ]
Rajkanna, Jeyanthy [1 ]
Sagi, Satyanarayana, V [1 ]
机构
[1] Peterborough City Hosp, Diabet & Endocrinol, Peterborough, England
关键词
epidermoid cyst; testis; klinefelter syndrome; case report; testosterone hormone; testicular; hypergonadotropic hypogonadism; x chromosome; adult teratoma; multi-disciplinary teams; TESTIS;
D O I
10.7759/cureus.11834
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Klinefelter syndrome is a rare chromosomal disorder with at least one extra X chromosome in males resulting in male hypogonadism, androgen deficiency and impaired spermatogenesis. It is associated with an increased risk of certain malignancies; including leukemia, breast cancer, non- Hodgkin's lymphoma and mediastinal germ cell tumors, however, testicular tumors are rare in men with Klinefelter syndrome. Testicular epidermoid cysts are rare benign tumors affecting the testes. We report a case of bilateral testicular epidermoid cysts in a 30-year-old man known to have Klinefelter syndrome. He had an incidental finding of bilateral hard irregular-surfaced testes during routine assessment for testosterone replacement therapy. Biochemical investigation confirmed primary hypogonadism and ultrasound imaging demonstrated bilateral solid testicular masses with no blood flow seen within the lesions. The patient went on to have a right-sided radical orchiectomy with left-side sparing. The histology revealed features in keeping with that of a testicular epidermoid cyst with no evidence of malignancy. The patient was commenced on testosterone replacement therapy. This case emphasizes the importance of routine physical examination of the male external and internal genitalia when considering testosterone replacement therapy.
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